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1220 Cards in this Set

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Best treatment for ventricular tachy in a pt with stable BP?
amidarone is drug of choice. lidocaine can also be used.
What type of arrhythmias can be treated by Digoxin?
atrial arrhythmias
Tx for sustained ventricular tachy with hemodynamic compromise?
Cardioversion
What role does carotid massage play in ventricular tachy?
None - useful for SUPRAventricular tachy (narrow complex)
What kind of pulse is found in aortic regurg?
bounding aka "water hammer"
What causes a bounding or water hammer pulse in aortic regurg?
AR is associated with an increased SV which produces an abrupt rise in the systolic BP and rapid distension of the peripheral arteries. Then during diastole, there is a regurg of blood back into the left ventricle, resulting in a low diastolic pressure and collapse of the peripheral arteries.
Fixed splitting of S2 plus a midsystolic pulmonary flow murmur?
ASD
Why is lidocaine not used prophylactically in patients with acute coronary sundromes to prevent ventricular fibrillation?
it increases the risk of asystole
3 most common causes of aortic stenosis?
senile calcific aortic stenosis, bicuspid aortic valve, and rheumatic heart disease.

S4 in aortic stenosis is common - atrial kick against a stiff left ventricle.
When is a pt at risk for ACUTE pericarditis after an MI?
first several days - diffuse ST elevations, esp with PR depressions are typical ECG findings.

Dressler syndrome is an immune-mediated pericarditis that can occur WEEKS to months after infarction.
Common complication 3-7 days after an MI?
ventricular free wall rupture - presents with rapid deterioration of the pt 2dry to pericardial tamponade -- pulseless electrical activity on ECG is common

OR

interventricular free wall rupture and papillary muscle rupture - presents with new onset systolic murmor
common LATE complication of anterior wall MI?
ventricular aneurysm - can occur days to months after the initial infarction.

will see persistent ST elevations on ECG. S/sx of CHF, ventricuar arrhythmias, mitral regur, and/or thrombus formation can be seen.
MILD hypovolemia can cause syncope in what population of pts?
elderly - they very poorly tolerate even what seems to be an insignificant loss of fluid - especially orthostatic syncope upon getting up in the morning.

BUN/Cr ratio is a useful indicator of dehydration.
Treatment of choice for DRessler's syndrome?
NSAIDS. Corticosteroids can be used in refractory cases or if NSAIDs are CI.

Anticoagulation should be avoided to prevent development of hemorrhagic pericardial effusion.
Most likely artery that is occluded in acute inferior wall MI?
Right coronary artery, especially if it is complicated by right ventricular infarction (hypotension) and bradycardia.
LAD occlusion causes?
anterior wall MI
What can confirm a diagnosis of malignant hypertension?
Presence of papilledema - always suspect malig HTN if very high BPs (>/= 200/140).

Pathologic change responsible for end-organ dmg is fibrinoid necrosis of small arterioles.
leading cause of mitral stenosis worldwide?
Rheumatic heart disease

The mitral stenosis classically presents later during pregnancy bc of the physiologically increased total blood volume. Pulmonary edema and atrial fib may also occur due to left atrial overload/enlargement.
Pharmacologic management of variant (or Prinzmetal's angina)?
calcium ch blockers and/or nitrates to prevent coronary vasoconstriction.

Non-selective beta blockers and aspirin should be avoided bc they can promote vasoconstriction. Aspirin may cause vasospasm via prostacyclin inhibition.
Greatest risk factor for variant angina?
smoking
When does variant angina classically occur?
at night and can be associated with transient ST elevation on ECG.
PITTING edema vs. non-pitting edema?
PITTING - due to increased movement of fluid from vascular space into interstitial space. Can be due to increased intravascular hydrostatic pressure (CHF, portal HTN), decreased plasma oncotic pressure (low albumin 2ndry to malnutrition, nephrotic sydnrome, cirrhosis), or increased capillary leak (burns, trauma, or infection).

non-pitting - due to lymphatic obstruction (lymphedema) or decreased lymphatic flow(myxedema from hypothyroidism)
First step in treating pt with a WITNESSED cardiac arrest?
defibrillation

if arrest is unwitnessed or greater than 4-5 minute lapse btn arrest and arrival of defibrillator, a 2-min trial of CPR should precede defibrillaiton.
tx for first degree heart block?
nothing - completely benign condition
A stenotic mitral valve causes increased left atrial pressure which in turn gets transmitted to the pulmonary vasculature. What symptoms can this increase in pulm vascular pressure cause?
exertional dyspnea, nocturnal cough, and hemoptysis (hemoptysis in particular should raise suspicion for mitral stenosis)
how do nitrates reduce chest pain in angina pectoris?
venodilation --> blood pools in systemic venous circulation --> decreases preload --> reduces ventricular volume and wall stress (stretch) --> decreased myocardial oxygen demand.

They also cause some ARTERIAL vasodilation with modest decrease in afterload and myocardial oxygen consumption but this is not main mechanism.
thiazide diuretic may cause electrolyte disturbances causing sudden syncope without warning signs. this is caused by?
ventricular arrhythmia - drug predisposis to this
s/sx of coarctation of the aorta?
majority of pts are asymptomatic - but common s/sx (when present) include headache, epistaxis, cold extremities, delayed femoral pulse, or HTN in the upper extremity. In adults, enlarged pulsatile collateral vessels may be palpated in the intercostal spaces anteriorly, in the axilla or in the interscapular area. Also, upper extremity may be preferentially well developed.
Almost pathognomonic for coarctation of aorta?
"3" sign -indentations of the aorta at the site of the coarctation and pre and post stenotic dilation along the left paramedian border.
Patent ductus arteriosus is associated with?
birth at high altitudes and maternal rubella infection.
aortic aneurysms present with what s/sx?
hoarseness, chest pain, dysphagia or a dry cough.
When is surgery indicated for an aortic aneurysm?
aneurysm > 6 cm in diameter, persistent pain, continued elevated BP or wide expansion of the aneurysm.
Why do pts with severe aortic stenosis have anginal chest pain?
due to increased myocardial oxygen demand 2dry to large left ventricular mass.
When is clopidogrel (plus aspirin) indicated for 2ndry prevention in a cardiac patient?
1) All patients with a UA/NSTEMI for at least 12 months (aspirin indefinitely)
2) post- PCI pts x 30 days for bare metal stents and 1 year for drug eluting stents. Drug eluting stents need a longer duration bc epithelialization occurs slowly.
How long is LMWH usually given post-MI?
first 48 hours typically
Classic physical exam findings for cardiac tamponade?
pulsus paradoxus and Beck's triad (hypotension, jugular venous distention, and muffled heart sounds)

pathophys: fluid fills in pericardial sac --> pressure riss above diastolic pressure of the ventricles --> ventricles less able to expand and accept venous return to the heart --> decreased preload, SV, and CO --> decrease in CO made worse by inspiration due to lower intrathoracic pressure --> more systemic venous blood return to right ventriclue --> intraventricular septum bows into the left vetricle causing further reduction of left ventricular filling
Why can a dual upstroke be present in HOCM?
occurs from midsystolic obstruction that develops as the heart contracts
What maneuver worsens the murmur of HOCM?
anything that decreases preload - valsava, standin g
Elevated BNP levels and an audible S3 are both signs of _____?
increased cardiac filling pressures due to volume overload.
Most useful test to assess coronary RE-occlusion after an MI?
CK-MB bc it returns to normal levesl within 1-2 days, while troponin T (genrally a more sensitive marker of cardiac injury) takes up to 10 days to return to normal after an MI.
Tx for hemodynamically stable SUPRAventricular tachy?
vagal maneuvers followed by adenosine and AV nodal blockers. adenosine decreases conduction through the AV node.

SVT should be suspected on ECG with a regular, narrow QRS complex tachy withOUT definite P waves.
What should be suspected in otherwise young healthy pts who develp s/sx of CHF including paroxysmal nocturnal dyspnea, dyspnea on exertion, peripheral edema, hepatomegaly, cardiomegaly, bilateral pleural effusions,a nd a third heart sound?
Dilated cardiomyopathy 2ndry to myocarditis should be high on the DDx. Coxsackie B virus is the most common cause.

Diagnosis is via echocardiogram which typically shows dilated ventricles and diffuse hypokinesia resulting in systolic dsyfunction (low EF).
Most effective lifestyle intervention for reducing blood pressure?
decreased consumption of alcohol. smoking cessation decreases a pt's risk of cardiovascular dz but does NOT improve blood pressure itself.
First line drugs for tx of cocaine-related cardiac ischemia?
benzodiazepines, nitrates, and aspirin - allays the anxiety and reduces the HTN and tachycardia

beta-blockers (Metoprolol) would be CI bc they aggravate cocaine-medited vasoCONStriction.
How long should a pt with an episode of rheumatic fever receive antibiotic prophylaxis with penicllin to prevent further attacks?
Treat until pt reaches age 18 to prevent repeat episodes which can worsen valvular function.
Most common cause of secondary HTN?
chronic oral contraceptive use - simply discontinuing its use can correct the problem
Tx for third degree heartblock?
pacemaker insertion

3rd degree or complete heart block is marked by complete indepenence of the P waves and QRS complexes.
Tx for subacute bacterial endocarditis?
empiric ABX until causative bacterium is identivied. Native valve bacterial endocardities is most commonly due to Streptococcus viridans, which is highly susceptible to IV penicillin G or IV ceftriaxone.
Intensive retrosternal pain that radiates to the back of the chest along with normal ECG strongly suggests?
aortic dissection - check BP in both arms and auscultate for diasolic murmur of aortic regurg. TEE is the preferred diagnostic tool (bc MRI and CT are time consuming) but before performing procedure, HTN should be controlled.
How does adenosine have diagnostic value in a suspected supraventricular tachycardia?
an SVT is usually terminated by adenosine whereas other tachycardias are simply slowed.
Review of renin-angiotensin-aldosterone axis...
renin is produced by the juxtaglomerular cells of the kidney in response to hypOperfusion. Renin cleaves angiotensinogen to agiotensin I. In turn, angiotensin I is converted into angiotensin II by ACE in the lungs. Angiotensin II is a potent vasoconstrictor. It also promotes vasopressin (ADH) release from the pituitary and aldosterone prodxn from the adrenal cortex. Aldosterone acts on the distal convoluted tubules and collecting ducts to promote sodium and water resorption (at the expense of potassium).
In a patient with an MI who develops a cold leg, one should get an ECHO to rule out?
thrombus in the left ventricle that may have embolized to the leg. An MI results in blood stasis in the akinetic part of the heart with resultant thrombus formation.
typical presentation for bacillary angiomatosis?
immunocompromised indvidual (e.g. AIDS, malignancy, undergoing chemo, organ transplant recipients) with non specific constitutional symptoms PLUS characteristic lesions of the skin and viscera (angioma-like blood vessel growths). This condition is caused by Bartonella henselae and Bartonella quintana. Antibiotic treatment causes lesion regression.
What should be suspected in a pt that has areflexic weakness in the upper extremities and dissociated anesthesia (loss of pain and temp with preserved position and vibration) in a "cape" distribution?
Syringomyelia - presence of a cavitary expansion of the spinal cord (known as a syringe) with destruction of the gray and white matter adjacent to and often communicating with the central canal. Most frequent site of involvement is the lower cervical or upper thoracic region. When syringes occur in the upper cervical cord and extend proximally to involve the medulla oblongata, the condition is called syringobulbia. Causes include congenital, trauma, inflammatory conditions,tumors, and idiopathic.
Strongest influence on long-term prognosis following an ST-elevation MI?
duration of time that passes before coronary blood flow is restored (via PTCA or fingrinolysis). Reperfusion injury can occur but benefits of reperfusion far outweigh the consequences of reperfusion injury.
Pt that presents with painLESS sub acute monocular vision loss?
DDx includes central retinal vein occlusion (CRVO) or central retinal artery occlusion (CRAO).

CRVO will show optic disk swelling, retinal hemorrhage, dilated veins, and cotton wool spots. CRAO shows pallor of the optic disk, a cherry red fovea, and boxcar segmentation of blood in the retinal VEINS.
Most common histologic lesion of diabetic nephropathy?
diffuse glomerulosclerosis but NODULAR glomerulosclerosis (with Kimmelstiel-Wilson nodules) is pathognomonic.

Dz progression can be slowed with strict glycemic control, treatment of HTN, and angiotensin axis blockade.
What can cause insoluble crystal precipitation in the tubular lumen leading to acute renal failure 2dry to renal tubular obstruction?
hyperuricemia from tumor lysis syndrome, indinavir, acyclovir, and sulfonamide therapy.

Inadequate hydration is a predisposing factor. Look for oliguria with elevated creatinine and BUN.
Best initial test in a patient with suspected hepatocellular carcinoma (typically caused by chronic viral hepatitis or cirrhosis)?
AFP which is frequently elevated in hepatocellular carcinoma but is NOT EXCLUDED by a normal AFP level. If AFP is elevated, imaging (CT or MRI) will be needed to detect the lesion. Biopsy may ultimately be necessary in many patients if a concerning lesion is found on imaging.

Note that ascites fluid cytology has a low yield for confirming diagnosis of hepatocellular carcinoma and generally not recommended.
Leukocytosis, anemia, and increased number of mature granulocytic forms (eg. segmented neutrophils and band forms on peripheral blood) with low leukocyte alkaline phosphatase score should raise suspicion for?
CML - typically seen after age 50. Presence of Philadelphia chromosome confirms dx.

The only other dzs that may cause a low leukocyte alkaline phosphatase are hypophosphatemia and paroxysmal nocturnal hemoglobinuria (PNH).
Elevated leukocyte alkaline phosphatase is characteristic of?
Leukemoid reaction
tartrate resistant acid phosphatase is present in ?
hairy cell eukemia
Adult treatment panel 3 recommendation for CHD or CHD risk equivalent (such as DM or PAD)?
Goal LDL < 100
Lifestyle modification @ >/= 100
Drug therapy @ >/= 130
Adult treatment panel 3 recommendation for 2+ risk factors for coronary heart disease?
Goal LDL < 130
Lifestyle modification @ >/= 130
Drug therapy @ >/= 160
Adult treatment panel 3 recommendation for 0-1 risk factors for coronary heart disease?
Goal LDL < 160
Lifestyle modification @ >/= 160
Drug therapy @ >/= 190
Risk factors for coronary heart disease?
men >/= 45
women >/= 55
HTN
cigarette smoking
HDL < 40
fam hx of premature CHD (male < 55, female <65)
CHD risk equivalents?
DM
symptomatic carotid artery dz
abdominal aortic aneurysm
peripheral artery dz
10-yr risk of CHD of 20% or higher
Decreases triglyceride levels and increases HDL concentrations?
Niacin - NOT considered first line for reducing LDL levels
Most common cause of fatal sporadic encephalitis in the U.S.?
Herpes encephalitis 2dry to HSV-1. Affects the temporal lobe of the brain and presents acutely (< 1 week) with focal neuro findings such as AMA, cranial nerve deficits, hemiparesis, dysphasia, aphasia, ataxia, or focal seizures. Fever is present in approx 90% of pts.

CSF analysis shows lymphocytic pleocytosis, increased number of erythrocytes (due to hemorrhagic destruction of the temporal lobe), and elevated protein levels. MRI is the preferred method of imaging as CT may be normal in up to 50% of pts. Focal EEG findings (prominent intermittent high amplitude slow waves) occur in > 70-80%.

PCR analysis of HSV DNA in the spinal fluid is the gold std of diagnosis.
India ink preparation is used to detect?
cryptococcal meningitis in immunocompromised patients.
What may simulate an iron deficiency anemia (microcytic/hypochromic) but with iron studies that reveal ELEVATED serum iron levels and decreased TIBC?
Sideroblastic anemia resulting from defective heme synthesis, most commonly due to pyridoxine-dependent impairment in early steps of protoporphyrin synthesis. Often caused by alcoholism or drugs such as isoniazid.

Microscopy reveals two gropus of RBCs ("dimorphic" RBC population) - microcytic and hypochromic.
Pt with signs of ischemia (parasthesia, change in temperature, and non-detectable radial arterial pulsations) BUT NORMAL neuro exam is suspicious for?
embolus of the upper extremity arterial bed, specifically the radial artery. Immediate anticoagulation with heparin and surgical intervention (i.e. embolectomy) are crucial bc can lead to tissue death and amputation if not effectively treated in hours.
Diagnostic study of choice in multiple sclerosis?
MRI which shows white matter dz
Reliable screening test for hemochromatosis?
Percent transferrin saturation (greater than 45%) and serum ferritin level (greater than 1000 microg/L).
Complications of hemachromatosis?
chronic liver disease or cirrhosis, hepatocellular carcinoma, diabetes, pancreatic insufficiency, skin pigmentation
First step in management of acute pyelonephritis?
Blood and urine cultures FIRST, followed by IV antibiotics.

Acute pyelonephritis can lead to gram-negative sepsis so it is important to determine the causative agent, evaluate for bacteremia, and check for drug resistant organisms.

Fluoroquinolones or ceftriaxones can be used for treatment.
When does acute pyelonephritis become complicated?
progression to renal corticomedullary abscess, perinephric abscess, emphysematous pyelonephritis, or papillary necrosis. Typically occurs in pts with DM, kidney stones, or other urologic abnormalities.
When is CT or ultrasound indicated in the mgmt of acute pyelo?
if fever or clinical symptoms persist after 48-72 hours of appropriate antimicrobial therapy to r/o obstruction, abscess, or other complications.
what is allergic conjunctivitis?
an acute hypersensitivity reaction caused by environmental exposure to allergens. Characterized by intense itching, hyperemia, tearing, conjunctival edema, and eyelid edema but NO vision disturbances. Usually a positive family or personal history of asthma, seasonal rhinitis, atopic dermatitis, food allergies, or urticaria. Condition usually subsides wi 24 hours even wo treatment. Topical antihistamines, artificial tears, and cool compresses can help.
What is atopic keratoconjunctivitis?
SEVERE form of ocular allergy with itching, tearing, THICK mucus d/c, photophobia, and blurred vision.
What is blepharitis?
chronic inflammatory condition involving lid margins bilaterally. Crusty d/c is seen clinging to lashes in ANTERIOR blepharitis whereas hyperemic lid margins with telangiectasias are seen in POSTERIOR blepharitis.
What is dacrocystitis?
infection of the lacrimal sac due to obstruction of the nasolacrimal duct. It is characterized by pain, swelling, tenderness, and redness in the tear sac area. Mucous or pus can be expressed.
Classic presentation of Guillain-Barre syndrome?
ascending paralysis, areflexia and sensory changes 3-4 wks after a URI or gastroenteritis, PLUS albumino-cytologic dissociation (elevated protein despite normal cell count). Also can have cranial nerve paralysis and autonomic dysfunction.
Tx for Guillan-Barre syndrome?
IV immunoglobulin and plasmapheresis.
Major signs/sx for Waldenstrom's macroglobulinemia:
1) increased size of the spleen, liver, and some lymph nodes
2) Tiredness, usually due to anemia
3) Tendency to bleed/bruise easily
4) night sweats
5) headache and dizziness
6) various visual problems (opthalmoscopy may show dilated, segmented, and tortuous retinal veins)
7) pain and numbness in the extremities due to a predominantly demyelinating sensorimotor neuropathy.
Diagnostic clues for Waldenstrom's macroglobulinemia?
an IgM spike on electrophoresis which causes hyperviscosity of the blood (seen for example by retinal vein engorgement).
Pts with multiple myeloma may present with similar symptoms but the involved immunoglobulins are usually IgG or IgA. Further, they rarely have hyperviscosity sindromes such as retinal vein engorgement.
Management of newly diagnosed iron deficiency anemia in an elderly pt?
Secondary to chronic GI blood loss until proven otherwise. Colonoscopy should be next step in mgmt. A single negative occult blood test does not exclude the possiblity of GI bleeding.
Clinical features of interstitial nephritis?
fever, rash, and arthralgias. May be accompanied by peripheral eosinophilia, hematuria, sterile pyuria, eosinophiluria, and urine WBC casts.

70% of cases are caused by drugs such as cephalosporins, penicillins, sulfonamides, sulfonamide containing diuretics, NSAIDs, rifampin, phenytoin, and allopurinol. Discontinuing drug is the treatment.
What drugs provide a survival benefit in CHF pts?
ACE-I, ARBs, beta-blockers, and spironolactones.

Digoxin and loop diuretics (furosemide) provide symptomatic relief but no survival benefit.
Warfarin inhibits?
synthesis of Vit K dependent factors II, VII, IX, X, protein C and protein S.
Antibiotic choice for prophylaxis/treatment of infections caused by human or dog bites?
Amoxicillin-clavulanate (covers polymicrobial infections)
Main mechanism of kidney damage in SLE?
immune-complex mediated which activates complement leading to low serum C3.
Mechanism of kidney damage in post-strep glomerulonephritis?
immune-complex mediated which activates complement leading to low serum C3.
Management of spontaneous subconjunctival hemorrhage?
A benign finding that requires no treatment. Minor bruising that may be due to simple trauma from rubbing eyes, violent coughing spells, or hypertensive episodes. Usually disppears in 24-28 hours.
Role of dihydropyridine calcium channel blockers (such as nifedipine) in ACS pts?
contraindicated bc can worsen cardiac ischemia via peripheral vasodilation and reflex tachy.

NON-dihydropyridines (diltiazem and verapamil) can be used in STEMI pts with ongoing ischemia after beta-blockers have been administered but even then, they do not improve mortality.
Classic findings of erysipelas?
sharply demarcated, erythematous, edematous, tender skin lesion with raised borders. Legs are most frequently-involved site.

Most frequently implicated organism is group A beta-hemolytic streptococcus (S. pyogenes).
Population most at risk of developing SLE?
young, african-american women aged 20-40 years.
common SLE s/sx?
fatigue, painLESS oral ulcers, non-deforming arthritis (commonly affecting MCP/PIP hand joints) in 90%, low grade fever, weight loss, malar or discoid rash, hematologic abnormalities (thrombocytopenia and leukopenia), serositis, and proteinuria.
What pathological mechanism underlies exophthalmos of Graves disease?
1) sympathetic nervous system mediated lid retraction.
2) autoimmune attack on extraocular muscles wherein lymphocytes infiltrate the EOMs and orbital fat causing edema, proliferation of local interstitial fibroblasts, and deposition of glycosaminoglycans. End result is fibrosis and edema with EOM enlargement that pushes the lobe outward.

May be bilateral or unilateral!

Eye "grittiness" or "sandiness" and excessive tearing may occur due to corneal exposure and keratitis resulting from inability to completely close eyelids over protruding eyeball.
First step in management of a diabetic ulcer?
Proper wound care and debridement followed by antibiotics.
Most common nephropathy associated with carcinoma?
Membranous nephropathy; however, minimal change disease is a well-known complication of Hodgkin's lymphoma.
Acanthosis nigricans is associated with?
1) insulin resistant states such as DM, acromegaly, obesity, and others
2) GI (or GU) malignancies
Reversible risk factors for premature atrial contractions?
tobacco and alcohol. beta-blockers are often helpful in pts who are symptomatic
Suspect what if there are signs of hypopituitarism plus headaches and bitemporal blindness?
craniopharyngiomas (benign suprasellar tumors).

In chidlren, retarded growth is the most prominent feature 2dry to low growth hormone and thyroid hormone. Sexual dysfunction is more prominent in adults. Women can present with amenorrhea. Tumor compresses optic chiasm causing bitemporal blindess. Headaches are due to an increased intracranial pressure.

TX is surgery and/or radiotherapy.
Tremor that is somewhat suppressed at rest and exacerbated toward the end of a goal-directed movement?
essential tremor-first line tx is propranalol especially if the pt is hypertensive. Other possibilities include anticonvulsants such as primidone and topiramate.
Tremor that is worst at rest and improves with intentional movement?
Resting tremor associated with Parkinson's.
Most common malignancy of the liver?
Metastasis from another primary source
Most common cause of hydatid cysts of the liver?
Cystic echinococcosis is cuased by the tapeworm Echinococcus granulosus mostly in immigrants or pts that live in the SW region of the country and are exposed to SHEEP and DOGS. Microscopic exam reveals encapsulated and calcified cyst that contains fluid and budding cells.
alpha feto protein is commonly elevated in which liver dz?
hepatocellular carcinoma
Suspect what if there is a solitary epithelial tumor of the liver (usually in the right hepatic lobe) in a middle-aged woman with a lengthy hx of oral contraceptive usage?
hepatic adenoma (benign condition)
Neoplasm of the liver characterized by vascular spaces that are lined with malignant cells?
hepatic angiosarcoma - rare neoplasm more common in older men exposed to toxins such as vinal chloride gas, arsenic compounds, and thorium oxide.
vomitus gastric contents are rich in?
hydrogen, chloride, and potassium
Remember what about heterophile antibodies used to dx infectious mono?
very sensitive and specific but may be negative early in illness.
Mechanism of hypercalcemia in pts with tumors that are metastatic to bone?
local osteolysis by production of CYTOKINES such as IL-1 and tumor necrosis factor (TNF).
Pathogenesis of chronic cough 2ndry to ACE-I?
Related to an accumulation of the inflammatory or proinflammatory mediators bradykinin, substance P, thromboxanes, and prostaglandins.
In mechanical ventilation, pO2 provides a measure of oxygenation and is influenced by _______ and ________ while pCO2 provides a measure of ventilation and is affected mainly by ________ and ________.
pO2: FiO2 and PEEP levels

pCO2: Respiratory rate and tidal volume.
Mechanical ventilation improves oxygenation by providing an increased fraction of inspired oxygen (FiO2) and by providing PEEP to prevent alveolar collapse.
Typical goal FiO2?
Initially, pts are usually given high FiO2 (~ 80% or 0.8), pending the results of the first blood gas analysis. Based on results, FiO2 should be decreased to prevent oxygen toxicity; typically below 50-60% is desirable. Goal is to maintain paO2 >/= 60!! PEEP can also be adjusted to increase/decrease the number of alveoli available for gas exchange and maintain adequate oxygenation.
Criterion for initiating home oxygen in COPD patients?
PaO2 < 55 mmHg or SaO2 < 88%.

Pts with signs of pulmonary htn or hematocrit > 55% should be started on home oxygen when the PaO2 < 60 mmHg.

The dose of oxygen should be titrated such that SaO2 is maintained at >90% during sleep, normal waking hours, and at rest. Survival benefits are significant when used for a minimum of 15 hours per day.
Acidosis accompanied by hypercarbia (elevated pCO2) and a normal/elevated serum bicarb is diagnostic of a?
respiratory acidosis (often caused by hypOventilation)

Note: post-ictal state can cause apnea/hypoapnea during prologned seizures or an aspiration event.
Pathogenesis of aspirin sensitivity syndrome?
a 'psuedo-allergic' reaction due to prostaglandin/leukotriene misbalance. Aspirin is a cyclooxygenase inhibitor --> arachidonate diverges from blocked COXs to a 5-lipoxygenase pathway --> accumulation of leukotrienes and changed prostaglandin/leukotriene balance triggers characteristic reactions (bronchoconstriction, polyp formation).

Tx includes avoidance of NSAIDs and the use of leukotriene receptor ANTagonists (drug of choice).
Very high yield!
Common cause of upper lobe cavitary lung lesions in immigrant patients?
TB
Recommended therapy for an acute bacterial exacerbation of COPD?
supplemental oxygen, inhaled bronchodilators (beta-2 agonests or anticholinergics such as ipratropium), broad-spectrum ABX, a 2-week corticosteroid taper, and smoking cessation.

Care must be taken with supplemental oxygen bc it can suprress the hypoxia-fueled respiratory drive in COPD pts.
An important cause of pneumonia in HIV/AIDS patients?
Pneumocystis jiroveci (carinii) pneumonia - hypoxia occurs 2ndry to alveolar and interstitial inflammation causing areas of V/Q mismatch. This manifests as an increase in the alveolar-arterial oxygen gradient.
Symptoms that help distinguish Legionella from other causes of community acquired pneumonia?
1) high-grade vever
2) GI symptoms
3) confusion
What will be a common finding on sputum gram stain for Legionella pneumophila?
Many neutrophils but no organisms bc it is a Gram-negative rod that stains poorly and is primarily intracellular.
Commonly spread by cooling towers and water supplies. Travel-associated infection is well-documented.
Diagnosis and treatment of Legionella pneumophila CAP?
Dx is confirmed by urine antigen testing or culture on charcoal agar. Tx with azithromycin or levofloxacin.
NEW clubbin in a pt with COPD often indicates?
lung cancer - interestingly finger clubbing is RARELY a feature of COPD.
Alveolar hypoventilation (as in COPD exacerbation) can cause?
confusion, somnolence, coma, and tonic-clonic seizures. Sedatives should be avoided in these pts as they can exacerbate alveolar hypoventilation.
Only two modalities shown to decrease mortality in COPD?
home oxygen therapy and smoking cessation
Non-cardiogenic pulmonary edema aka ARDS can develop in what settings?
sepsis, severe bleeding, pneumonia, toxic ingestion, or burns when release of inflammatory mediators cause increased alveolar capillary permeability and resultant pulmonary edema.
How can cardiogenic pulmonary edema be distinguished from non-cardiogenic?
Measurement of pulmonary capillary wedge pressure (PCWP).

PCWP > 18 mmHg -- pulmonary edema 2dry to impaired left ventricular fxn.

PCWP < 18 mmHg -- NON-cardiogenic etiology
Non-invasive positive pressure ventilation (NIPPV) should be tried before intubation and mechanical ventilation in a pt with respiratory distress because?
Better alveolar ventilation and less fiatigue of respiratory muscles.

Recommended in pts with a pH < 7.35 or PaCO2 > 45 mmHg or respiratory rate > 25/min.
When is non-invasive positive pressure ventilation contraindicated?
pts who are septic, hypotensive, or dysrhythmic.
Characteristic change in FEV1/FVC in COPD patients versus restrictive lung dz?
decreased in COPD due to reduction of mainly FEV1.

normal ratio in restrictive lung dz.
DLCO (diffusion capacity) may help distinguish between what two COPD entities?
it is decreased in emphysema and normal in chronic bronchitis
Suspect what with presence of a mobile cavitary mass (crescent radiolucency next to a rounded mass) in the lung which presents with intermittent hemoptysis?
Aspergilloma - cavitations are due to destruction of underlying pulmonary parenchyma. Mobile mass is due to debris and hyphae coalescing to form a fungus ball.
Number one cause of chronic cough in nonsmokers?
postnasal drip
Most specific test available for GERD?
24-hour pH recording - usually used in pts with chest pain or chronic cough when esophagoscopy is negative.
Suspect what in COPD pts with catastrophic worsening of their respiratory symptoms?
spontaneous secondary pneumothorax - destruction of alveolar sacs and formation of large airspaces (generally in the UPPER lobes) are predisposing factors.
In addition to panlobular emphysema, pts with alpha-1 antitrypsin deficiency are also at risk for _________?
liver disease

note: AAT is an enzyme that counteracts NEUTROPHIL ELASTASE. Uninhibited elastase causes bullous changes of the lungs.
Goal INR in pts with prosthetic heart valves?
2.5-3.5
how long should a pt with a VTE be treated with oral anticoagulation?
At least 3 months if there is a reversible risk factor and for 6-12 months in pts with idiopathic DVT.
The proximal deep veins include?
iliac, femoral and popliteal
Potential therapies for patients with obesity hypoventilation syndrome?
weight loss, ventilator support, oxygen therapy and progestins (a respiratory stimulant).
cause of obesity hypoventilation sydrome aka Pickwickian sydrome?
decreased lung compliance
Suspect what if a loculated, abnormally contured effusion with adjacent pulmonary consolidation is seen on CXR?
empyema, an intrapleural collection of pus - most commonly due to bacterial seeding from an untreated pneumonia.

Often unrepsonsive to antibiotics bc infection progresses to a mixed aerobic and anaerobic bacterial population.
How can bronchiectasis be identified on CT?
presence of dilated bronchi with thickened walls. Hemoptysis, sometimes massive to the point of requiring bronchial artery emoblization is a potential complication.
Treat an ANaerobic lung infection (suspected due to foul-smelling sputum) with what ABX?
Clindamycin
Common responsible antigens in hypersensitivity pneumonitis?
aerosolized bird droppings ("bird facier's lung") and molds associated with farming ("farmer's lung")
Typical presentation of hypersensitivity pneumonitis?
acute episodes of cough, breathlessness, fever, and malaise that occur within 4-6 hours of antigenic exposure. Chronic exposure may cause weight loss, clubbing, and "honeycombing" of the lung. Management is avoidance of the responsible antigen.
In pneumonia pts, placing the consolidated lung segment in a dependent position can increase right-to-left shunt. Why?
Alveoli of consolidated lung segments are filled with exudate and do not participate in pulmonary gas exchange, so their ventilation is essentially zero, i.e. blood perfusing consolidated areas is not oxygenated. These positions decrease the patient's oxygen saturation levels which is the same theory as an increased R-to-L shunt.
Mainstay therapy for ARDS?
Mechanical ventilation with LOW tidal volumes and PEEP. Levels up to 15 of PEEP may be necessary in ARDS pts.

Note: potential complications of PEEP include barotrauma and tension pneumothorax.
What may help distinguish asthma from COPD?
FEV1 measurement before and after bronchodilator treatment - demonstrates reversibility if greater than 15% improvement of FEV1 is seen. Reversibility is more consistent with asthma; however a certain subset of pts with COPD also show positive bronchodilator response indicating an overlap of pathophysiology may exist.
Presentation of blastomycosis?
pulmonary and CXR findings similar to TB and histoplasmosis however systemic blastomycosis may cause skin ulcerations and lytic bone lesions.

Note: found endemically in the Great Lakes, Mississippi and Ohio River basins. Wisconsin has the HIGHEST rate of infection.
Coccidiodomycosis is endemic to what part of the US?
Southwestern

Causes fungal infection of the lungs that can lead to fever, cough, and night sweats. X-pulmonary manifestations include skin, skeleton, and MENINGES.
Definitive diagnostic test for bronchiectasis?
high-resolution CT scan
Suspect what in a pt with an asymptomatic pulmonary nodule that resides in Mississippi?
Histoplasma capsulatum - endemic to Mississippi and Ohio River valleys and Central America. Found in soil with a high concentration of bird or bat guano droppings.

Note: chronic cavitary pulmonary histoplasmosis (which is a fatal form) usually develps in older COPD pts. Disseminated histoplasmosis is seen in immunocompromised pts.
Bacteria commonly responsible for acute exacerbation of COPD?
S. pneumoniae, H. influenza, and M. catarrhalis. All pts suspected with a bacterial pneumonia should have a CXR as the first step and then ABX wo waiting for sputum gram stain or cultures.
How long before Warfarin becomes therapeutic in treatment of a VTE?
4-5 days which is why concurrent heparin for 5 days should be used.
Drugs of choice for in-patient treatment of community acquired pneumonia?
newer antipneumoccocal quinolones like levofloxacin or moxifloxacin.

For outpatient therapy, either azithromycin or doxycyline can be used.
What is an important interaction of ciprofloxacin and erythromycin with theophylline?
decreases theophylline clearance and raises plasma concentration with possibility of theophylline toxicity. Toxicity manifests as CNS timulation (headache, insomnia), GI disturbance (N/V), and cardiac toxicity (arrhythmia). Mechanisms responsible for toxicity may include phosphodiesterase inhibition, adenosine antagonism, and stimulation of epinephrine.
Typical FEV1/FVC ratio in COPD?
less than 0.7
Suspect what with asymmetric breath sounds immediately after intubation?
Right mainstem bronchus intubation - a relatively common complication of endotracheal intubation. Ideally the tip of the endotracheal tube should be between the vocal cords and the carina. CXR confirms diagnosis and slight withdrawal of the tube resolves the complication.
Left-sided endocarditis commonly sends septic emoli to where?
regions rich in blood supply such as the brain, kidneys, liver, and spleen.
Drug of choice in a pt who presents with stable angina AND hypertension?
beta-blocker - increases the threshold for the development of an anginal episode and controls the hypertension. They are also believed to be cardioprotective bc they decrease the sympathetic output to the heart.
What makes a test reliabile?
similar results on repeat measurements. reliability is maximal when random error is minimal.
What makes a test valid or accurate?
The test's ability to measure what it is supposed to measure. To determine validity, results must be compared to those obtained from the gold standard test.
When should a patient be screened for bladder cancer?
never due to its relatively low incidence and poor positive predictive value.
The two phases involved in the pathogenesis of metabolic alkalosis?
generation phase - vomiting results in the loss of gastric fluids high in HCl, NaCl, and water. The loss of hydrogen ions as HCl results in unbalanced retention of HCO3- leading to a metabolic alkalosis.

maintenance phase - volume loss in the vomitus causes a decrease in the ECV volume leading to decreased renal perfusion pressure. The kidneys respond by increasing activation of the renin-angiotensin-aldosterone system. Aldosterone promotes retention of water at the expense of H+ and K+ loss in the urine. This action of aldosterone is what causes the hypokalemia and a contraction alkalosis.

First step in management - restoration of the ECF volume with IV normal saline and potassium.
Possible mechanism of adverse effects such as myopathy of statins?
decreased synthesis of products unrelated to cholesterol products such as reduced CoQ10 production.
Mechanism of action of statin?
inhibits HMG-CoA reductase which is the rate-limiting enzyme in the synthesis of cholesterol that converts HMG-CoA to mevalonate.
When is an AIDS pt at risk for CMV retinitis?
When CD4 count falls below 50. Pts may be asymptomatic with characteristic fundoscopic findings of yellow-white patches of retinal opacification and hemorrhages. Tx is ganciclovir or foscarnet.
Suspect what if there is necrosis involving the inner layers of the retina that appear as white, fluffy lesions surrounded by retinal edema and vitritis?
ocular toxoplasmosis in an immunocompromised host. More than 50% will also have encephalitis.
Suspect what in an older pt that presents with fever, malaise, and a burning/itching sensation of the periorbital region with examination revealing a vesicular rash in the distribution of the cutaneous branch of the first divison of the trigeminal nerve?
Herpes zoster opthalmicus caused by varicella-zoster. Usually in the elderly but may also be a presenting sign in HIV pts that predict increased risk of progression to AIDS.
A saw-tooth pattern of P waves that do not all conduct QRS complexes?
atrial flutter due to a re-entrant rhythm within the atria. A 2:1, 3:1, or 4:1 heart block is often seen.
A P-wave that is morphologically distinct from those originating in the sinus node; will also occur prematurely and may not conduct to the ventricles?
atrial ectopy
Suspect what in a pt with diffuse telangiectasias, recurrent severe epistaxis, and widespread AV malformations in the mucous membranes, skin, GI tract or even the liver, brain, and lung?
Osler-Weber-Rendu sydrome aka hereditary telangiectasia.

Note: AVMs in the lungs can shunt blood from the right to the left side of the heart causing chronic hypoxemia and a reactive polycythemia. They can also present as massive hemoptysis.
The use of anti-estrogen, tamoxifen, reduces the risk of recurrence of breast cancer from the original site or a new breast site, but increases the risk of ________, _______, and _______?
endometrial cancer, uterine sarcoma and venous thrombosis.

Tamoxifen has a mixed agonist and antagonist activity.
Diarrhea due to Vibrio parahaemolyticus is usually transmitted by the ingestion of ?
seafood including shrimp, crab, and raw oysters
Post-splenectomy pts are at increased risk for sepsis from encapsulated organisms due?
impaired antibody-mediated opsonization in phagocytosis - antibodies produced by germinal center plasma cells enter the systemic circulation to bind specific antigens and facilitate phagocytosis via opsonization which is not possible in asplenic pts.
Fever every 48 hours occurs with what type of malaria?
P. vivax and P. ovale
Fever every 72 hours occurs with what type of malaria?
P. malariae
Type of malaria with no periodicity?
P. faciparum - most malaria deaths are due to faciparam malaria
"Smudge cells" are characteristically seen in?
CLL - a disease of mostly older patients. Pts are often asymptomatic and diagnosed due to incidental finding of lymphocytosis with a peripheral blood fil showing small, mature-appearing lymphocytes. Symptomatic pateints usually c/o lymphadenopathy.
What indicates a poor prognosis in CLL?
thrombocytopenia
Chronology of disease progression in measles caused by Paramyxovirus?
1) exposure to the virus transmitted via respiratory droplets.
2) Prodrome of cough, coryza, and conjunctivitis after 10 days
3) Koplik's spots appear ~48 hours BEFORE skin rash and slowly fade once the rash appears.
4) Rash is initially over the face and then spreads to cover trunk and extremeties.

Koplik's spots are red spots with bluish specks over the buccal mucosa opposite the premolar tooth.
Complications are pneumonia, Vit A deficiency, and bronchiectasis. Late complications include immunosuppression and subacute sclerosing panencephalitis.
What type of thyroid cancer has the propensity for early hematogenous spread to the lung, brain, and bones?
Follicular thyroid cancers - they can be differentiated from follicular adenomas by histopathological demonstration of invasion of the capsule and blood vessels.
Most common thyroid malignancy?
Papillary throid cancer characterized by psammoma bodies. Fine needle aspiration biopsy reveals large cells with ground glass cytoplasm, and pale nuclei with inclusion bodies and central grooving.
Prognosis of papillary thyroid cancer?
excellent even in the presence of metastasis
sensory and reflex abnormalities on PE generally indicate?
neuropathies due to peripheral nerve problems
What should be suspected with absent/diminished reflexes at rest but improved muscular strength with repetitive tasks?
PREsynaptic membrane damage, i.e. Lambert-Eaton syndrome
paraplegia/quadriplegia with sensory abnormalities and urinary retention/incontinence on PE generally indicates?
some type of myelopathy originating from damage to the spinal cord
Even with therapeutic range INRs, there is significant risk of _______ with warfarin treatment?
Retroperitoneal hematoma - should be suspected with back pain and hemodynamic compromise. Dx with an abdominal CT.
DOC for trigeminal neuralgia?
carbamazepine - effective in approx 80% of cases.

Note: Risk of aplastic anemia; therefore routine CBC should be included in follow up management.
Tx for cluster headaches?
Sumatriptan and high-flow oxygen
Untreated hyperthyroid pts are at risk for?
Rapid bone loss resulting from increased osteoclastic activity (from direct effects of the thyroid hormones) AND cardiac tachyarrhythmias including A-fib.
Toxic adenomas causing hyperthyroidism do not cause proptosis as in Grave's disease bc?
there is no autoimmune process underlying the disease
Glucocorticoids cause what classic changes on blood cells?
1) Leukocytosis due to neutrophilia
2) Diminished eosinophils
3) Lymphopenia
DOC for treatment of myasthenia gravis?
oral anticholinesterase such as pyridostigmine or neostigmine. Atropine (anticholinergic agent) can be used to prevent muscarinic side effects of anti-ACh therapy.

Note: edrophonium can be used to diagnose MG but is no longer used
What is a complication that can arise in pts requiring multiple blood transusions or immediately after surgery that manifests as hyperactive deep tendon reflexes, muscle cramps, and sometimes convusions?
hypOcalcemia resulting from volume expansion and hypOaluminemia PLUS decreased IONIZED calcium due to citrate binding.

Note: severe hypOmagnesemia may mimic hypocalcemia bc it causes decreased PTH secretion and decreased peripheral responsiveness to PTH.
When is aspirin indicated as the ONLY antithrombotic therap in a pt with atrial fibrillation?
IN an otherwishe healthy pt with "lone" atrial fibrillation in the absence of other risk factors for stroke (CHADS2).
Indications for thyroid function tests?
1) hyperlipidemia, esp high LDL
2) unexplained hypOnatremia
3) elevated serum muscle enzymes
Drugs of choice for treating/preventing chemo-induced N/V?
serotonin ANTagonists that block 5HT3 receptors such as ondansetron. Corticosteroids are sometimes added to the regimen for better prophylaxis.
A rare malignancy that often arises in Hispanic and Southwestern Native American females with a hx of gallstones?
Gallbladder carcinoma - typically diagnosed after cholecystectomy. If discovered while still confined to the lamina propria of the gallbladder, a simple cholecystectomy results in a cure rate of 73-100% and is considered sufficient treatment.
Negative predictive value varies with?
pretest probability of a dz - a pt with high probability of having a dz will have a low NPV whereas a pt with low probability of having a dz will have a high NPV.
Known side effects of anti-tubercular therapy?
peripheral neuropathy due to pyridoxine deficiency (Vit B6) and hepatitis
Light's criteria to distinguish an exudative pleural effusion from one that is transudative:
1) pleural fluid protein/serum protein ration > 0.5
2) pleural fluid LDH/serum LDH ratio > 0.6
3) pleural fluid LDH greater than 2/3 of the upper limit of normal for serum LDH
How to determine if a pleural effusion is complicated?
Complicated fluids have:
1) a positive gram stain or cultures
2) pH < 7.2
3) glucose level < 60 mg/dL

Complicated effusions require a chest tube drainage.
Prophylaxis for a cluster headache?
prophylaxis is key to mgmt and includes verapamil, lithium, and ergotamine. Tx of acute attacks is inhalation of 100% oxygen and subcutaneous sumatriptan.
Tx for acute exacerbations of MS?
corticosteroids; beta-interferon or glatiramer acetate is used to decrease the frequency of exacerbations.
Evaluation for diarrhea in HIV-infected pts should include?
stool culture, examination for ova and parasites, and test for C. difficile toxin.
Suspect what in a pt over 50 years old with pain and stiffness in the neck, shoulders, and pelvic girdle with an elevated ESR and morning stiffness lasting OVER 1 hour?
polymyalgia rheumatica - treatment when NOT associated with giant cell arteritis is low-dose prednisone.

Note: pts indicate that pain is in the soft tissues and not the joints.
Characteristic findings in brain death?
ABSENT cortical and brain stem functions such as pupillary light rxn, heart acceleration after atropine injection, or spontaneous respiration.

The spinal cord may still be functioning; terhefore, deep tendon reflexes may be present.
Management of pts with probable benign prostatic hyperplasia based on hx and rectal exam?
urinalysis and serum creatinine to assess for infection, obstruction, or hematuria. Abnormalities warrant furter investigation.
Life threatening complication of succinylcholine used during rapid-sequence intubation?
Hyperkalemia leading to life-threatening arrhythmias - should not be used in pts at high risk for hyperkalemia such as those with crush/burn injuries more than 8 hours old (due to high risk of rhabdomyolysis), demyelinating syndromes like Guillain-Barre, and tumor lysis syndrome.

Vecuronium or rocuronium are better choice in these pts.
Most common cause of death in acromegaly?
cardiovascular accounting for ~ 38-62%.

acromegaly results from: high GH-->excess prodxn of IGF-1 --> excessive/abnormal bone and soft tissue growth including the heart leading to cardiomyopathy
What can help prevent contrast-induced nephropathy in pts with a hx of DM or chronic renal insufficiency (elevated baseline creatinine)?
Adequate IV hydration with isotonic bicarbonate or normal saline AND administration of acetylcysteine.

Contast-induced nephropathy presents as a transient spike in creatinine within 24 hours of contrast administration with a return to normal renal function within 5-7 days.
Suspect what in a pt older than 60 years with back pain that radiates to the buttocks/thighs and numbness/parasthesias that are worse during walking and lumbar extension and better with lumbar flexion?
Lumbar spinal stenosis due to two factors:
1) enlarging osteophytes at facet joints
2) hypertrophy of the ligamentum flavum

Dx via MRI.
Common extracolonic manifestations of inflammatory bowel dz?
1) skin findings such as erythema nodosum and pyoderma gangrenosum.
2) episcleritis
3) arthritis
4) cholangitis

p-ANCA is positive in ulcerative colitis.
What do inflammatory bowel dz and ankylosing spondylitis have in common?
HLA-B27 and presentation of arthritis is similar (low back pain/stiffness worse in the morning and improved with activity; plain radiographs show sacroiliac joint inflammation).
Suspect what with sharply localized pain over the anteromedial part of the tibial plateau just below the joint line of the knee (with possible complaints of exacerbation of pain while sleeping on one's side)?
Anserine bursitis - the result of abnormal gait, overuse, or trauma. A valgus stress test does NOT reproduce pain, thereby ruling out damage to the medial collateral ligament and XR will be normal. Treatment is rest, ice, and maneuvers that reduce pressure on the bursa. Corticosteroid injections into the bursa are helpful.
Most appropriate step in management of a pt with suspected recurrence of gouty arthritis?
synovial fluid analysis bc gouty arthritis cannot be reliably distinguished from septic arthritis (which can rapidly dstro the involved joint) or pseudogout based upon history and exam alone.

Synovial fluid analysis will reveal a WBC count of 2,000-50,000/ml and needle-shaped, NEGatively birefringent crystals under polarized light. Gram stain and culture will be negative.
Most appropriate step in managment of a young patient presenting with progressive low back pain and spinal stiffness of >3 month duration that typically improves with exercise?
XR demonstrating fused sacroiliac joints and/or bamboo spine caused by ankylosing spondylitis. It is a seronegative (negative for rheumatoid factor and ANA)spondyloarthropathy with a strong association with HLA-B27 (>90%).
Most likely diagnosis in a pt that is awakened by severe, acute pain in the great toe and describes occasional pruritus that can be "unbearable" after a hot bath?
Polycythemia vera-related gout. Myeloproliferative disorders are common causes of uric acid overproduction that can precipitate attacks of gouty arthritis.

Note: Polycythemia vera commonly causes splenomegaly and characteristic pruritis (due to histamine release from an increased number of circulating basophils).
Treatment of fibromyalgia?
Improves with TCAs and exercise.

Seen in women 20-50 years and is associated with fatigue, poor sleep, and depression.
A common complication of advanced osteoporosis?
compression fracture of the vertebrae - usually manifests as acute back pain withOUT any obvious preceding trauma. PE will show local tenderness and a normal neuro and musculoskeletal exam.

Note: Glucocorticoids predispose a pt to osteoporosis.

Note: Absent ankle reflex can be seen in elderly pts as part of the normal aging process.
Common complication of giant cell or temporal arteritis?
aortic aneurysms due to the involvement of the branches of the aorta. Pts should be followed with serial chest X-rays.
signs and symptoms of temporal arteritis?
symptoms such as headache, jaw claudication, muscle fatigue, and visual disturbance. PE may show scalp tenderness and a decreased temporal artery pulse. ESR is greater than 50 typically.
Prophylaxis for gout?
Allopurinol and probenecid - there is some risk of inducing uric acid RENAL stones with probenicid, so allopurinol is the first line agent.
Presentation of drug-induced serum sickness?
Symptoms of fever, urticaria, and arthralgias begin 1-2 weeks after administration of a drug such as penicillin, amoxicillin, TMP-SMX or cefaclor. Most commonly occurs in young children when a VIRAL infection is treated with an antibiotic agent.
How does degenerative joint disease (osteoartritis aka "wear and tear" arthritis) present?
Adults over 40 with indolent but progressive pain of the hands and weight bearing joints that is exacerbated by exercise and relieved by rest BUT sometimes with MILD morning stiffness (LESS than 30-60 minutes unlike rheumatoid arthritis). Unlike autoimmune processes, systemic symptoms are absent. Effusions may occur but joint will remain cool to touch. Bony crepitus, bony enlargement, and painful or decreased range of motion are common on exam. Synovial fluid analysis will reveal fewer than 2,000 WBC, no organisms, and no crystals.
What will a plain film of an osteoarthritic joint show?
narrowed joint space with osteophyte formation and subchondral sclerosis/cysts.
How many WBCs can be seen on synovial fluid analysis with septic arthritis?
> 50,000
What should be suspected with proximal muscle weakness PLUS an elevated ESR AND CK?
an inflammatory myopathy such as polymyositis or dermatomyositis - confirmed by muscle biopsy. Classic cutaneous findings include a rash over the face (with periorbital edema known as heliotrope sign), chst and lateran neck (called shawl sign), and on the knucles, elbows, and knees (Gottron's sign). Lichenoid papules overlying joints are known as Gottron's papules. Treated with high-dose corticosteroids.
Auto-antibody associated with dermatomyositis?
anti-Mi-2 (against helicase).
What type of regular screening should a pt with dermatomyositis undergo?
Cancer screening - over 10% will develop an internal malignancy, most commonly an ovarian cancer.
Suspect what if a woman in the fifth or sixth decade complanes of keratoconjunctivitis sicca (xerophthalmia, dry eyes), xerostomia (dry mouth), and other associated problems such as dental caries and difficulty swallowing?
Sjogren syndrome - diagnosed by the either the presence of lymphocytic infiltration of the salivary glands or serum autoantibodies against SSA (Ro) and/or SSB (La).

PE may reveal enlargement and firmness to palpation of the salivary glands. Due to the antimicrobial and lubricating properties of normal amounts of saliva, there is an increased incidence of dental caries and difficulty swallowing with Sjogren's syndrome.
Next step in management in a pt with rheumatoid arthritis?
disease modifying anti--rheumatic drugs (DMARDs): methotrexate is the initial drug of choice.
What is diagnostic of rheumatoid arthritis?
Lab testing shows rheumatoid factor and anti-cyclic citrullinated peptide, while XR shows joint erosions, uxt-articular osteoporosis and narrowing of joint spaces (most commonly affecting the proximal interphalangeal and metacarpophalangeal joints).
initial drug of choice for osteoarthritis?
acetaminophen
Most frequent cause of prosthetic joint septic arthritis?
Staphylococcus aureus via hematogenous spread.
Important adverse effect with use of methotrexate?
Macrocytic anemia, sometimes even pancytopenia. Routine peripheral blood counts should be taken every 3 months.

Methotrexate works by inhibiting dihydrofolate reductase which can lead to folate depletion. The addition of folic acid supplements can alleviate or prevent this side effect.

Other side effects include, nausea, stomatitis, rash, hepatotoxicity, interstitial lung dz, alopecia, and fever.
Who is at highest risk for osteomyelitis?
injection drug uses, patients with sickle cell anemia, and immunosuppressed pts. The vertebrae is frequently involved site in IV drug abusers.

Platelet count is often high as a marker of inflammation/stress and the ESR is significantly elevated (>100) as well. MRI is the most sensitive diagnostic study. Treatment is long term IV ABX with or without surgery.
Most common septic arthritis in young, sexually active pts?
Neisseria gonorrhea which may present in one of two ways:
1) an asymetric polyarthrits (often with tenosynovitis and skin rash) OR
2) isolated purulent arthritis affecting one or a few joints.
**In some, an asymmetric polyarthritis will precede purulent monoarthritis.

Dx may be confirmed by gram stain of synovial fluid, blood cultures, urethral cultures or skin cultures.
What is tennis elbow?
Lateral epicondylitis that manifests as pain with supination or extension of the wrist and point tenderness just distal to the lateral epicondyle. Can be caused by a variety of activities that involve repeated forceful wrist extension and supination such as backhand in tennis or use of a screwdriver.

Underlying pathophysiology: degeneration of the extensor carpi radialis brevis tendon near the lateral epicondyle.
What does "neuropathic claudication" in lumbar spinal stenosis mean?
Exacerbation of leg symptoms with walking (similar to PVD). However, unlike PVD, the symptoms are positional. Extension (e.g. standing and DOWNhill walking) exacerbate symptos bc this narrows the spinal canal, whereas fexion (e.g. sitting and UPhill walking) improves symptoms bc it widens the spinal canal.
Manifestations of sarcoidosis?
cough, dyspnea, erythema nodosum, antrior uveitis, and acute polyarthrits.

CXR shows hilar adenopathy with or without reticulonodular infiltrates. Bioposy will reveal NONcaseating granulomas. Elevated serum ACE may be elevated.
Treatment for symptomatic sarcoidosis?
Systemic glucocorticoids. Asymptomatic sarcoidosis is often followed without treatment due to the high rate of spontaneous remission.
Lab and radiographic evidence that supports the diagnosis of psuedogout?
fever, leukocytosis with a left shift, and chondrocalcinosis (calcified articular cartilage). Synovial fluid analysis (needed for diagnosis) IDs rhomboid, positively birefringent crystals.
Settings that may precipitate pseudogout?
trauma, surgery, or medical illness.
Characteristics of SLE induced arthralgia/arthritis?
Affects greater than 90% of pts but is considered NON-deforming. Most commonly involves hands or knees. It is a migratory arthritis with pain that is often disproportionate to objective physical findings.
First line therapy for reactive arthritis?
NSAIDs
Triad for reactive arthritis (Reiter syndrome)?
conjunctivitis, Asymmetric oligoarthritis, and nongonococcal urethritis. Arthritis often involves knee and sacroiliac spine.

Note: mucocutaneous lesions (ulcers) and enthesitis (Achilles tendon pain) are common too!
Red flags that warrant investigation rather than conservative treatment of back pain?
1) Age over 50
2) Hx of previous cancer
3) Unexplained weight loss
4) Pain greater than 1 month duration
5) Nighttime pain causing difficulty with sleep
6) No response to previous therapy
7) Neurologic syndrome

**Initial test of choice is plain films to look for lytic lesions and compression fractures.
Pain aggravated by pushing, pulling, lifting the arm above the head, and lying on the affected shoulder is most likely due to?
Rotator cuff tear vs. rotator cuff tendonitis. Lidocaine injection can help distinguish btn the two - amelioration of pain with injection indicates tendonitis whereas no improvement indicates a tear. MRI is the study of choice for confirmation of diagnosis.
Most likely cause of proximal muscle weakness with associated fatiguability, tremor, anxiety, and weight loss?
Thyroid myopathy (in this case hypErthyroidism but can also be caused by hypothyroidism). Causes predominantly proximal muscle weakness. Search for additional symptoms of thyroid dysfunction to confirm diagnosis.
How to distinguish btn thyroid myopathy and myasthenia gravis causing proximal muscle weakness?
MG will more than likely involve eye and bulbar musculature whereas thyroid myopathy will not.
How can a viral arthritis be distinguished from other symmetric inflammatory arthritides (namely RA and SLE)
It tends to resolve within 2 months.

Positive rheumatoid factor may occur in RA, viral or bacterial infection, malignancy, and in normal individuals.

ANA is sensitive for SLE but can also be present in RA, hepatitis, and HIV. Weakly positive ANA can be found in approx 5% of normal individuals!

Treatment for viral arthritis is NSAIDs. Antiviral therapy is unnecessary as symptoms are self-limited.
What should be suspected if a pt complains of pain with active range of motion of the shoulder, passive internal rottion, and forward flexion but with no signs of deltoid atrophy?
Subacromial bursitis - typically occurs in the setting of chronic microtrauma to the supraspinatus tendon caused by overhead work and repeated overhead movements of the arm during work or sporting events. The tendon is traumatized by compression btn the acromian and the humeral head, and its vascular supply may be temporarily compromised during such episodes of compression. The subacromial bursa lies btn the acromian and the tendon of the supraspinatus muscle.
A tear of the proximal end of the long head of the bicep tendon is associated with?
rotator cuff injury and typically occurs during forceful flexion of the arm. Patients present with a prominent bulge in the midportion of the upper arm. Axillary nerve injury may occur as a result of anterior dislocation of the humerus out of the glenoid fossa.
The axillary nerve supplies?
the deltoid and the teres minor with motor innervation - palsy of this nerve would result in paralysis and ultimately denervation atrophy of these muscles.
Precipitating factors for osteonecrosis? (aka aseptic necrosis, avascular necrosis, ischemic necrosis, and osteochondritis dessicans)
Chronic corticosteroid use and chronic excessive ingestion of alcohol account for over 90% of cases. Other factors include trauma and antiphospholipid syndrome.

Pathogenesis: bone vasculature is disrupted --> bone and bone marrow infarction --> trabecular thinning --> ultimately causing collapse of the affected bone.

**process may take months to years and presents with ANTERIOR hip pain worsened by activity and relieved rest with progressive limitation of range of motion. Will ultimately cause joint instability and pain at rest.

MRI is the most sensitive test for this condition.
Suspect what if a pt complains of painful joints with the formation of tumor-like protrusions with lesions draining chalky white material?
Chronic tophaceous gout - begins with asymptomatic hyperuricemia and progresses to gouty arthritis, typically affecting the great toe first (called podagra). Uric acid crystals form in the renal tubules and collecting system resulting in nephrolithiasis. Urate crystals may deposit in the soft tissues forming tumors known as tophi which can ulcerate to drain chalky material.

Note: diuretics (especially HCT) have a hyperuricemic effect from hypovolemia-associated enhancement of uric acid reabsorption in the proximal tubule.
Suspect what with normal serum calcium and phophate levels BUT INCR alk phos and urinary hydroxyproline levels?
Paget disease of bone (osteitis deformans) - disorder of accelerated and disordered osteoclastic bone resorption of uncertain etiology. Incr bone resorption --> disorganized formation of lamellar or woven bone (inherently weaker than normally formed bone) --> pain and bowing of lower extremity weight bearing bones --> hypertrophy of skull compresses the vestibulocochlear nerve causing deafness.

Lab abnormalities include elevated alk phos plus urinary markers of bone degradation such as hydroxyproline, deoxypyridinoline, N-telopeptide and C-telopeptide.
CREST syndrome refers to what constellation of findings?
1) Calcinosis cutis - localized dystrophic deposition of calcium in the skin that appear as nodules typically on the upper extremities. May ulcerate and drain a chalky material like chronic tophaceous gout.
2) Raynaud phenomenon - acute bouts of digital ischemia in response to cold and may lead to digital necrosis.
3) Esophageal dysmotility - dysphagia and GERD
4) Sclerodactyly - fibrosis of skin on fingers distal to MCP joints resulting in "shiny appearance," flexion contractures, and joint pain.
5) Telangiectasias - "mat-like" patches most common on the face and palms.
What are firm, flesh-colored, NON-tender nodules found over pressure points such as the elbow and extensor surface of the proximal ulna?
rheumatoid nodules - almost all will have positive rheumatoid factor.
What are Heberden and Bouchard nodes?
hard, bony nodules over the DIP and PIP joints, respectively.
Mechanism involved that leads to joint trauma in neurogenic arthropathy aka Charcot's joint?
nerve damage - process starts with decreased pain, proprioception, and temperature perception. As normal neurologic input is lost, pts unknowingly traumatize their weight bearing joints. XR's will show loss of cartilage, osteophyte development, and loose bodies. Associated pain is typically mild. Management includes treating the underlying disease and providing mechanical devices (special shoes) to assist in weight bearing and decrease further trauma.
Diseases that can lead to neurogenic arthropathy aka Charcot's joint?
DM, peripheral nerve damage, syringomyelia, spinal cord injury, B12 deficiency, or tabes dorsalis.
In chronic gout, what may an XR of the joints show?
punched-out erosions with overhanging rim of cortical bone known as "rat bite" lesion.
Typical population that is affected by ankylosing spondylitis?
Young men (2-3:1 ratio compared to women) under 40 years of age (most frequently btn 20-30 years). Symptoms are typically worst in the morning and improve as the day progresses. Associated findings iclude arthritis of the peripheral joints and anterior uveitis.
Side effects of methotrexate treatment (first line drug for RA)?
stomatitis (ulcers), nausea, abdominal pain, fever, LFT elevation 2dry to hepatotoxicity and anemia 2dry to myelosuppression.
triad of Felty syndrome?
Rheumatoid arthritis, splenomegaly, and granulocytopenia with neutrophil < 2,000/mm3). Granulocytopenia generally does not occur until symptoms of arthrits have been present for over 10 years.
Suspect what in a patient over 50 years with NEW-onset temporal headache, jaw claudication, vision loss, or symptoms of polymyalgia rheumatica?
temporal arteritis - immediate empiric treatment with high dose steroids is necessary, especially to prevent visual loss.

Note: ESR will be elevated and temporal artery biopsy will provide definitive diagnosis.
Important preventative measures to prevent gouty attacks?
1) alcohol cessation: ethanol is metabolized to lactate, which competes with urate for renal excretion, leading to accumulation of urate in the body.
2) eating a low purine diet
3) avoiding drugs such as diuretics and pyrazinamide.

Tx of ACUTE attack: NSAIDs, colchicine, or steroids.
What are Baker cysts?
A result of excessive fluid production by an inflamed synovium that occurs in cases of RA, osteoarthritis, and cartilage tears. Excess fluid accumulation expands in the poplitieal bursa, creating a tender mass in the popliteal fossa. They can occasionally burst to release their contents into the calf, resulting in an appearance similar to a DVT.
Most prominent extraarticular manifestation of ankylosing spondylitis?
anterior uveitis
Bone demineralization is present in _________ and _________.
osteomalacia and osteoperosis.

osteomalacia is due to inadequate serum vitamin D, calcium or phosphorus resulting in demineralized osteoid. Osteoperosis is due to a decrease in bone mineral density.
Suspect what in a pt that has traveled to or is from an endemic area and presents with RUQ pain, diarrhea, leukocytosis, elevated alk phos, and tender liver mass on abdominal CT?
Amebiasis - most pts are asymptomatic but can develop liver abscess, dysentery, and other organ develpment. Those with liver abscess typically present with 1-2 weeks of fever, RUQ pain that starts wi 5 months of returning from an endemic aria, dysentery (1/3 of pts), and occasionally jaundice (<10% of pts).

Diagnosis is confirmed with ultrasound, CT, or MRI of SOLITARY liver lesion. Leukocytosis (>10,000) or an elevated alk phosphatase is also supportive. Serologic testing for antibodies should be performed to definitively r/o a pyogenic abscess. While awaiting serology results, treatment with oral metronidazole should be started which results in a cure for >90% within 7-10 days. If tests are negative or pt does not improve, alternative testing such as percutaneous drainage to rule out pyogenic abscess can be done.
Treatment for pyogenic abscess of liver?
Drainage and tx with oral metronidazole PLUS IV ceftriaxone.
POST cholecystectomy pain is due to one of three reasons:
1) common bile duct stone
2) sphincter of Oddi dysfunction
3) functional causes

Abnormal alkaline phosphatase or dilatation of biliary tree observed on ultrasound are indicators of either CBD stone or sphincter dysfunction. ERCP would be indicated to confirm and treat the condition, either through stone removal or sphincterotomy. No evidence of LFT abnormalities or dilation of biliary tree indicates functional pain with no obvious organic basis. Tx symptomatically with analgesics and reassurance.
Three major types of gallstones?
1) cholesterol
2) pigment
3) mixed

**cholesterol and mixed stones together comprise 80% of all gallstones in the Western population.
Pathogenesis of gallstones?
Water-INsoluble cholesterol is secreted in bile and converted into soluble micelles by bile acids and lecithin. Gallbladder hypomotility or excess cholesterol:bile salt ratio can cause cholesterol to precipitate into insoluble crystals which form gallstones.
Risk factors for formation of pigment gallstones?
chronic hemolysis (like in sickle cell anemia), chronic biliary tract infection or parasite infection; and advanced age.
Protective factors against development of gallstones?
low-carb diet, physical activity, consumption of caffeinated coffee, and aspirin or other NSAID usage.
Dx of cholelithiasis?
best confirmed with ultrasound. Tx for symptomatic cholelithiasis is laparoscopic cholecystectomy.
Treatment options for pregnant pts who experience repeated attacks of biliary colic?
cholecystectomy, preferably during the second trimester OR bile salt such as ursodeoxycholic acid to dissolve cholesterol stones. Gallstones frequently recur once treatment with bile salt is stopped, however.
Gallstones are common in what population?
fat, female, fertile woman of forty years.
Consider what diagnosis if a pregnant woman c/o intense pruritus, especially significant on the palms and soles and worse at night?
intrahepatic cholestasis - a fxnl disorder of bile formation that develops in the second and third trimesters of pregnancy and is characterized by intense, often intolerable generalized pruritus, especially significant on the palms and soles and worse at night.

Total bile acids are typically elevated and may be the only finding. If other liver studies indicating stasis are abnormal, it may include elevated alkaline phosphatase and total/direct bilirubin. Serum aminotransferases may be quite high, which requires ruling out viral hepatitis.
Treatment for intrahepatic cholestasis of pregnancy?
Relief and preventing complications! Relief is provided using ursodeoxycholic acid as it increases bile flow and can relieve pruritus. Maternal prognosis is good as condition resolves shortly after delivery with no hepatic sequelae. Condition may recur in subsequent pregnancy and affected women are at increased risk for developing gallstones.

Reducing complications is centered around the fetus bc known complications include fetal prematurity, meconium-stained amniotic fluid, and intrauterine demise. Preferred approach is early delivery once fetal lung maturity is established.
What is Reye syndrome?
fatty liver with encephalopathy seen exclusively in children younger than 15 years, and is preceded by a URI with influenza or varicella. Tx with aspirin (salicylates) significantly increases likelihood of developing Reye syndrome.

Characterized by headache, nausea/vomiting, excitability, delirium, combativeness, hypOglycemia, liver failure, and progressive CNS damage.
Morphological changes seen in liver showing Reye syndrome?
extensive fatty vacuolization of the liver withOUT inflammation due to diffuse mitochondrial injury.
Lab abnormalities found in Reye syndrome?
Elevated aminotransferases, ammonia levels, PT prolongation, hypOglycemia, and metabolic acidosis.
Treatment of Reye syndrome?
glucose with FFP and mannitol to cerebral edema.
Balloon degeneration with polymorphic cellular infiltrates seen in the liver indicates?
ACUTE alcoholic hepatitis
Panlobular mononuclear infiltration with hepatic cell necrosis with confluent hepatic cell necrosis connecting adjacent lobules (described as "bridging necrosis") in the liver indicates?
ACUTE viral hepatitis
CHRONIC active hepatitis has what morphological appearance?
mononuclear inflammatory cells that extend from portal areas to disrupt the limiting periportal plate of hepatocytes undergoing necrosis -- called "piecemeal" necrosis.
First diagnostic step in a pt suspected to have pancreatic cancer?
Abdominal ultrasound followed by abdominal CT if sono is nondiagnostic.
Prognosis of pancreatic cancer?
typically presents late and has a poor prognosis, even in those with potentially resectable mass. Five-year survival rate ranges from 10-30%, depending on nodal status.
Major risk factors for pancreatic carcinoma?
chronic pancreatitis, smoking, DM, and hereditary predisposition.
Typical presentation of pancreatic carcinoma?
Tumors of the pancreatic body or tail = pain and weight loss

Tumors of the pancreatic head = steatorrhea, weight loss, and jaundice.

**Pain is usually a dull upper abdominal (epigastric) pain that radiates to the back
Classic PE signs of pancreatic carcinoma?
Often PE is unremarkable aside from jaundice with an abdominal mass or ascites (present in only 20%). Metastatic disease may be indicated by a nontender but palpable gallbladder (Courvoisier's sign) OR left supraclavicular adenopathy (Virchow's node).
Tumor markers which may be elevated in pancreatic carcinoma?
CA 19-9 - but this can also be elevated in pts with jaundice and NO pancreatic cancer which reduces its utility as a screening tool. Postoperative monitoring of pancreatic cancer with CA 19-9 may be helpful in evaluating response to chemotherapy.
Most common underlying causes of cirrhosis?
chronic alcohol abuse and chronic viral hepatitis (mostly hep C but can also be caused by hep B).
How is infection with Echinococcus granulosus diagnosed?
Serology and CT showing "eggshell" calcification of a hepatic cyst.
Treatment of hydatid cysts from Echinococcus granulosus?
Aspiration is NOT indicated due to risk of anaphylactic shock secondary to spilling of cyst contents. Treatment is surgical resection under the cover of albendazole.
Classic criteria for acute cholecystitis?
1) usually develops after a large or fatty meal
2) sudden appearance of steady pain in the epigastrium or RUQ
3) Pain may radiate to right scapula
4) positive Murphy's sign - sharp arrest of inspiration with gallbladder palpation.
5) fever, vomiting, and leukocytosis.
6) Total bili may range from 1-4 mg/dL, and serum aminotransferases and alk phos are often mildly elevated.
Most likely cause of acute cholecystitis?
2ndry to gallstone formation in over 90% of cases, most commonly arising when a gallstone impacts in the cystic duct.

gallstone impacts cystic duct --> ingestion of fatty foods --> contraction of gallbladder against obstructed cystic duct causing severe colicky pain --> tissue behind duct obstruction becomes inflamed 2dry to bacterial overgrowth 2dry stasis --> subsequent ischemia can lead to gangree or perforation or abscess formation.
What should all patients with cirrhosis be screened for?
Esophageal varices by endoscopy. Primary prophylaxis to reduce the risk of bleeding is via beta blockers.
Two most common causes of acute pancreatitis?
alcohol and gallstones.

other major causes include medications and hypertriglyceridemia.
Why is ultrasound more sensitive than CT for detecting gallstones?
Many stones have bile and are isodense, therefore would not be seen on CT scan.
Initial diagnostic test in all pts suspected of experiencing a first attack of acute pancreatitis?
Ultrasound of the RUQ to search for the presence of gallstones. Abdominal CT scan is used to confirm the diagnosis of acute pancreatitis and identify complications.
What is a HIDA scan and what is it used for?
it helps track production and flow of bile from the liver to the intestine - an excellent tool to diagnose cystic duct OBSTRUCTION (cholecystitis). Not as useful in detecting nonobstructive gallstones (cholelithiasis).

Also known as cholescintigraphy, hepatobiliary scintigraphy, and hepatobiliary scan.
What is charcot's triad and what does it indicate?
Triad of fever, severe jaundice, and RUQ abdominal pain.

Indicates acute ascending cholangitis - an infection of the common bile duct.
What is Reynold's pentad and what does it indicate?
Charcot's triad of fever, severe jaundice, RUQ pain PLUS confusion and hypOtension.

Indicates suppurative cholangitis with need for urgent biliary decompression/drainage preferably by ERCP. Therapy typically includes sphincterotomy with stone removal and/or stent insertion.
Initial diagnostic test employed in suspected acute ascending cholangitis?
Ultrasound.
Treatment of acute ascending cholangitis?
after diagnosis with ultrasound, immediate supportive care and broad spectrum ABX. Sufficient in 80% of patients. Pts who do not respond to this treatment should undergo ERCP for biliary drainage. Early drainage can significantly decrease morbidity and mortality.
Most likely cause of acute pancreatitis in a patient with NO hx of alcohol use or gallstones but with the presence of eruptive xanthomas?
hypertriglyceridemia (over 1,000 mg/dL) - confirm with FASTING serum lipid profile
Downsides to using ursodeoxycholic acid for treating symptomatic cholelithiasis over surgical correction?
expensive, therapy is needed for several months before gallstones dissolve, 50% recurrence rate once the treatment is stopped.
What type of hyperbilirubinemia is found in Dubin-Johnson syndrome?
Conjugated!
How may a patient with Dubin-Johnson syndrome clinically present?
Icterus is evident but is typically otherwise normal. Icterus may be so mild that it only becomes evident in the context of a trigger such as illness, pregnancy, or oral contraceptive usage. ROUTINE labs are usually unremarkable including LFTs. Interestingly serum bilirubin can range from 2-5 mg/dL, but can ALSO be normal or extremely elevated! Diagnosis requires a direct bilirubin fraction of at least 50% and confirmation of high levels of urine coproporphyrin I (as opposed to coproporphyrin III in normal individuals). Total urine copropophyrin is in normal amounts.
Gross and histological appearance of liver in Dubin Johnson syndrome?
Grossly the liver is strikingly black. Histology shows dense pigment composed of epinephrine metabolites within the lysosomes.
What does hyperestrogenism in cirrhosis lead to?
gynecomastia, testicular atrophy, decreased body hair, spider angiomas, and palmar erythema
What stages of liver disease from alcoholism can be reversed by cessation?
fatty liver (steatosis), alcoholic hepatitis, and early fibrosis.

True cirrhosis with regenerative nodules is irreversible.
Two main causes of CONjugated hyperbilirubinemia?
1) intrahepatic causes from either intrahepatic obstruction (e.g. viral or autoimmune hepatitis, alcoholic hepatitis, drug reactions, 3rd trimester of pregnancy or postop states).

OR congenital defects in hepatic excretion (e.g. Dubin-Johnson, Rotor)

2) extrahepatic causes
What helps distinguish between the different causes for conjugated hyperbilirubinemia?
dominant aminotransferase elevation = hepatocellular disease

vs.
dominant alk phos elevation = intra- or extrahepatic biliary obstruction.

Those with predominant alk phos elevations should have an ultrasound or CT scan to rule out extrahepatic obstrcution. If nondiagnostic, next step is ERCP or PTC (percutaneous transhepatic cholangiogram).
Blood transfusions before what year are at risk for hep C or hep B?
screen for hep C if before 1992.

screen for hep B if before 1986.
What should be suspected in a patient with a palpable mass in the epigastrium 4 weeks after the onset of acute pancreatitis?
pseudocyst - not a true cyst as they lack an epithelial lining. Inflammatory fluid comprised of enzymes (amylase, lipase, enterokinase), tissue, and debris enclosed by a thick fibrous capsule. If amylase leaks out, serum amylase becomes markedly elevated.

Often resolves spontaneously so drain only if it persists for > 6 weeks, is greater than 5 cm in diameter, or becomes secondarily infected.

Note: ultrasound is the preferred means of imaging.
Treatment for hepatic encephalopathy?
1) correct precipitating factors such as hypOvolemia, GI bleeding, hypokalemia, metabolic alkolosis, hypoxia, sedative usage, hypoglycemia, and infection.

2) Lower blood ammonia level - typically with lactulose (a disachharide) that acidifies colonic contents thereby converting absorbable ammonia into nonabsorbable ammonium ION (an ammonia trap). Non-responders can be placed on ornithine-aspartate infusion or oral sodium benzoate.
3) Reduced-protein diet is recommended but not drastic limitation bc can lead to negative nitrogen balance.
Single most important test to assess the FUNCTION of the liver?
PT bc all clotting factors (except VIII) are made in the liver.
What would a progressive decrease in liver transaminase levels indicate?
either recovery from liver injury or that few hepatocytes are functional.
Marked increase in transaminases is indicative of?
ongoing tissue destruction in the liver.
Two drugs approved for treatment of CHRONIC hepatits B and what is an important predictor of response to these drugs?
interferon and lamivudine in patients with persistently elevated ALT levels, detectable serum HBsAg, HBeAg, and HBV DNA.

Degree of elevation of serum ALT is most important predictor of response to interferon and lamivudine - serum ALT should be more than 2 times the upper limit for a favorable response.

Note: in general, lamuvidine is more convenient (oral) with fewer side effects than interferon.
Vanishing bile duct syndrome (aka ductopenia) indicates?
primary biliary cirrhosis usually - rare!
Why does cirrhosis sometimes lead to decreased TSH, T4, and T3?
Primary pituitary failure -- hypothalamic-pituatary dysfunction can occur in pts with cirrhosis!
What is hepatic hydrothorax?
Transudative pleural effusions in patients with cirrhosis which are NOT 2dry to any underlying cardiac or pulmonary disease. Generally much more common on the right side and is thought to occur 2dry to small defects in the diaphragm which permit abdominal ascites fluid to pass into the pleural space.

Primary treatment is therapeutic thoracentesis followed by a salt restricted diet and diuretics. If that fails, the next best treatment is a transjugular intrahepatic portosystemic shunt (TIPS).
ALL chronic hepatitis C with elevated ALT, detectable HCV RNA, and histological evidence of chronic hepatitis of at least moderate grade are candidates for antiviral therapy with?
interferon and ribavirin - combination therapy has shown to be more beneficial than monotherapy.
Most common diseases causing liver metastasis?
primary tumors of the GI, lung and breast
Most important reversible risk factor for pancreatic cancer?
smoking

Note: alcohol consumption, gallstones, and coffee intake are not risk factors for pancreatic cancer.
What confirms diagnosis of Wilson's disease?
Gold standard for diagnosis is liver biopsy that demonstrates quantitative hepatic copper levels. More commonly, diagonsis is confirmed by the presence of low serum ceruloplasmin (particularly < 20 mg/dL) PLUS increased urinary copper excretion or Kayser-Fleischer rings.
Treatment for Wilson's dz?
First line meds include copper chelators like d-penicillamine or trientine. Oral zinc also helps as it prevents copper absorption. Liver transplantation may be the only option if there is fulminant hepatic failure or dz that does not respond to pharmacotherapy.
Pathogenesis of Wilson's dz?
genetic mutations causing poor copper metabolism by reducing the formation and secretion of ceruloplasmin and by decreasing the secretion of copper into the biliary system. Copper accumulates within the liver causing free radical damage and eventually leaks out and deposits in other tissues including the basal ganglia (hepatolenticular degeneration) and cornea.
The most serious form of acute pancreatitis that can lead to systemic hypotension and eventual shock?
Pancreatic necrosis - locally released and activated pancreatic enzymes can increase vascular permeability within and around the pancreas, leading to the loss of a large volume of plasma into the retroperitoneum. Release of pancreatic enzymes and other inflammatory mediators into the circulation can also cause SYSTEMIC inflammation, widespread vasodilation, capillary leak, and resultant hypotension.

Requires aggressive fluid resuscitation and ABX.
What serological marker helps diagnose acute hepatitis B during the "window" period when HBsAg has disappeared but anti-HBs has not appeared?
IgM anti-HBc. The IgG fraction of anti-HBc signals recovery from disease.
What signals active viral replication and infectivity of hepatitis B?
HBeAg - detectable shortly after appearance of HBsAg. Tends to disappear shortly after aminotransferase levels peak and before HBsAg is eliminated, and is followed by the appearance of anti-HBe. Should it persist for more than 3 months, there is increased likelihood of chronic hepatitis B.
What marker suggests the cessation of active viral replication and low infectivity in hepatitis B virus?
Anti-HBe
Risk factors for the development of pancreatic cancer?
family hx, chronic pancreatitis, smoking, DM, obesity, and a diet high in fat.

Alcoholism and gallstones are NOT risk factors.
What are choledochal cysts?
congenital abnormalities of the biliary tree characterized by dilation of the intra and/or extra hepatic biliary ducts or both. Most cases are related to an anomalous pancreaticobiliary junction, which leads to weakness and dilatation of the biliary wall due to the reflux of alkaline pancreatic secretions into the biliary tree.

Initial investigation of choice is an ultrasonogram followed by CT or MRI as needed.
Treatment for benign hepatic adenomas?
General consensus for all symptomatic hepatic adenomas is surgical resection. Complete regression of the tumor can happen with discontinuation of oral contraceptives but growth, rupture (risk approaches 40%), and malignant transformation (risk approaches 8-13%) can also take place.

Note: biopsy is contraindicated bc of risk of hemorrhage.
Where is the primary infection in a pt who has an amebic liver abscess?
in the colon leading to bloody diarrhea; the ameba is transported to the liver by portal circulation leading to liver abscesses.
First step in management of acute variceal bleeding?
Establish vascular access with two large bore IV needles or a central line. Fluid resuscitation should begin until necessary blood products can be transfused.

Next minimize risk of aspiration by securing airway and initiating gastric decompression with nasogastric aspiration.

Finally, control bleeding. Medical control of bleeding can start with vasoconstrictors like terlipressing (synthetic analogue of vasopressin), ocreotide, or somatostatin. Control of bleeding is established in 80% though rebleeding is very common especially during the 6 weeks following the initial hemorrhage.
What does fresh frozen plasma contain?
All clotting factors and plasma proteins and provides volume in hypotensive states.
What does cryoprecipitate contain?
factor VIII, Factor XIII, fibrinogen, and von Willebrand factor.
Suspect what in a pt with evidence of atherosclerotic vascular dz that presents with abdominap pain followed by bloody diarrhea but have MINimal abdominal exam findings?
ischemic colitis - most commonly in the splenic flexure bc it is supplied by end arteries.
Patients with ulcerative colitis should undergo routine surveillance for what?
colon cancer with yearly colonoscopies beginning 8-10 years after diagnosis.
An elevated _______ in a pt with ulcerative colitis should raise suspicion for?
an elevated alkaline phosphatase level raises suspicion for primary sclerosing cholangitis.
Suspect what in a pt with a 5-month hx of episodic retrosternal pain lasting about 15 minutes and precipitated by emotional stress and hot or cold food?
Diffuse esophageal spasm - diagnosed via manometry (motility study) that should repetitive, non-peristaltic, high amplitude contractions that are either spontaneous or after ergonovine stimulation.
Suspect what in a pt with cirrhosis and ascites that presents with fever and lethargy?
spontaneous bacterial peritonitis (SBP) - can be a subtle presentation. Fever and subtle changes in mental status are the most common signs with abdominal pain often LESS prominent than in peritonitis of other etiologies.

Diagnose with paracentesis - requires positive ascites fluid culture and PMN level greater than 250/mm3. Paracentesis should be done before ABX therapy. E. coli and Klebiella are the most common organisms - treat with third generation cephalosporin.
Suspect what in a pt with multiple episodes of thrombosis withOUT a clear precipitating factor?
hypercoagulability (clue can be elevated PT/PTT and fibrin split products).

In a younger patient the cause may be genetic whereas in an older patient the cause may be a primary malignancy.
triad of carcinoid syndrome:
flushing, valvular heart disease, and diarrhea

Note: elevated serotonin and its metabolites 5-hyroxyindole acetic acid (5-HIAA) are present in the blood and urine.
Pts with carcinoid syndrome are at risk of developing what vitamin deficiency?
niacin - due to the increased formation of serotonin from tryptophan. Tryptophan is needed to make niacin.

3 D's of niacin deficiency: diarrhea, dermatitis, and dementia
Suspect what in a pt with an enlarged NON-tender gallbladder and evidency of biliary obstruction?
carcinoma of the head of the pancreas - CT scan is the best initial test.
first step in management of uncomplicated diverticulosis?
high fiber intake
Suspect what in a pt with a hx of GERD that hs difficulty swallowing solids by not liquids withOUT anorexia or weight loss?
peptic esophageal stricture - caused by body's reparative response to chronic exposure to gastric acid. Strictures tend to appear as symmetric and circumferential narrowings on endoscopy.

Note: Adenocarcinoma generally occurs in pts who have had GERD for >20 years and presents with weight loss and Asymmetric narrowing of the esophageal lumen.
What type of peptic ulcer gets better after meals and what type gets worse after meals?
dudoenal ulcers = better after meals

gastric ulcer = worse after meals.
Treatment for duodenal ulcer disease?
90% are infected with H. pylori so ABX (amoxicillin plus clarithromycin) for eradicate causal organism and a proton-pump inhibitor for acid suppression.
Why does total parenteral nutrition increase the risk of gallstones?
TPN bypasses the gut therefore normal stimuli (fatty acids and protein in the duodenum) for the release of cholecystokinin (CCK) is impaired. CCK typically stimulates contraction of the gall bladder and bile release into the gut lumen. Without CCK, gall bladder stasis results in bile sludge which can lead to gall stone formation.
Suspect what in the absence of perstaltic waves in the lower 2/3 of the esophagus and significant decrease in lower esophageal sphincter tone?
esophageal dysmotility associated with scleroderma.

characteristic clues: "sticking sensation" in the throat or dysphagia accompanied by heartburn.
How to diagnose lactose intolerance?
Many ways:
1) Positive hydrogen breath test (after ingestion of lactose)
2) positive stool test for reducing substances
3) low stool pH and increased stool osmotic gap.

Note: there is NO steatorrhea
Most common cause of intermittent and occult lower GI bleeding in pts over the age of 65?
Angiodysplasia - a controversial clue may be a systolic ejection murmur at the right second intercostal space, most likely representing aortic stenosis. Can be seen on colonoscopy but often missed. Angiography is the gold standard test but rarely performed.
How can C. difficile-induced colitis be diagnosed?
cytotoxin assay in stool. Treat with oral/IV metronidazole. Oral (but NOT IV) vancomycin can also be used.
Lab tests that can help confirm hepatorenal syndrome?
Elevated creatinine and VERY low URINE sodium (< 10 mEq/L). Also, the absence of protein and blood in the urine is helpful bc it makes intrinsic renal disease less likely.
Pathogenesis of hepatorenal syndrome?
Pts with severe liver dz can develop generalized systemic vsodilation thought to be 2dry to generation of nitric oxide in the splanchnic circulation due to portal hypertension. This reduced peripheral vascular resistance causing renal hypoperfusion and pre-renal renal failure.
Anti-endomysial or anti-gliadin antibodies indicate?
celiac dz
anti-scl-70 antibodies indicate?
scleroderma
anti-centromeric antibodies indicate?
CREST syndrome
anti-mitochondrial antibodies indicate?
primary biliary cirrhosis
signs and symptoms of malabsorpton due to celiac dz?
1) bulky, foul-smelling floating stool
2) loss of muscle mass or subQ fat
3) pallor 2dry to iron deficiency anemia
4) bone pain due to osteomalacia
5) easy brusing due to vit K deficiency
6) hyperkeratosis due to Vit A deficiency.

Fatigue and weight loss are also common complaints.
Suspect what with steatorrhea and with a hx of severe intermittent epigastric pain?
chronic pancreatitis - look for alcohol consumption.
Differential for a pt with dysphagia for BOTH solids and liquids, as well as regurgitation?
Achalasia and pseudoachalasia (2dry to a neoplasm at the gastroesophageal junction).

Achalasia can be diagnosed with imaging studies showing a markedly dilated esophagus with decreased peristaltic contractions and smooth, "bird beak" tapering of the DISTAL esophagus. Achalasia results from degeneration of the neurons within the esophageal wall that control peristalsis. It is usualy idiopathic but can be 2dry to systemic disease (e.g. Chagas' disease, amyloidosis, and sarcoidosis).

An older pt (over 60) that also has weight loss should be evaluated for an underlying neoplasm via endoscopy.
What is toxic megacolon?
Symptoms of acute colitis with radiologic evidence of colonic dilation. Can rapidly progress to colonic perforation; therefore it is a medical emergency.
MCC of toxic megacolon?
ulcerative colitis.
Treatment for toxic megacolon?
it is a medical emergency - IV steroids are the drug of choice. Also, nasogastric decompression, IV fluids, antibiotics and bowel rest is needed.
Indication for esophagoscopy in management of GERD?
1) Empiric therapy with acid-suppressing drugs fails
2) pt has features of "complicated" disease (e.g. dysphagia, odynophagia, weight loss, overt or occult bleeding, and iron deficiency anemia) in addition to the typical symptoms of GERD (e.g. heartburn, regurgitation, or sour/bitter taste).
When is esophageal pH monitoring used for the management of GERD?
when empiric therapy fails AND endoscopy (aka esophagoscopy) is negative.
Diagnostic clues to chronic inflammatory diarrhea (such as IBD)?
weight loss and inflammatory changes in the blood such as anemia, elevated ESR, acute phase reactants, and reactive thrombocytosis. Positive occult blood or positive stool leukocytes are also important clues bc they are usually absent in other types of diarrhea (such as secretory and osmotic).
Suspect what in a pt with back pain, anemia, renal dysfunction, and elevated ESR?
multiple myeloma. another characterisitc finding in MM is hypErcalcemia from bone lysis caused by plasmocyte-released humoral factors.
Manifestations of hypERcalcemia?
severe constipation, anorexia, weakness, increased urination, or neurologic abnormalities (e.g. confusion or lethargy).
Always consider ________ as a cause of constipation.
hypERcalcemia
What explains the "shifting" phenomenon of abdominal pain from the peri-umbilical to the right lower quadrant that is classic for acute appendicitis?
In the initial stages, only the viscera are inflamed. Afferent visceral pain fibers from the appendix accompany sympathetic nerves and enter the spinal cord at the T10 segment which explains the peri-umbilical pain. Subsequent inflammation of the parietal peritoneum and skeletal muscles cause somatic pain which is well localized (RLQ) and more severe in intensity.
Stepwise approach to treatment for ascites:
1) sodium and water restriction
2) spironolactone
3) loop diuretic (not more than 1 L/day of diuresis bc can cause hepato-renal syndrome)
4) frequent abdominal paracentesis with/without albumin infusion (2-4 L/day, less aggressive if renal function is borderline).
Important risk factors for adenocarcinoma of the esophagus versus squamous cell carcinoma of the esophagus?
adenocarcinoma - Barrett's esophagus and GERD

squamous cell CA - smoking and alcohol are important ones among many others
What should be suspected in an adult immigrant patient who presents with high-grade fever, a severe sore throat with odynophagia and drooling, stridor upon respiration and tenderness to palpation over the larynx?
Epiglottitis - can still occur by Hib (especially in those from other countries) or Streptococcus pyogenes.
What part of the GI does Crohn's disease involve?
any component from the mouth to the anus, characteristically with skip areas of involvement. Even apthous mouth ulcers can be a component of the disease.

Note: Granulomas are identified pathologically in up to 30% of patients with Crohn's disease.
Suspect what in an elderly patient with poorly controlled diabetes that presents with ear pain and drainage?
Malignant otitis externa - most commonly caused by Pseudomonas aeruginosa. Ear pain and drainage is not responsive to topical medications. Granulation tissue may be seen within the ear canal. Progression of infection can lead to osteomyelitis of the skull base and destruction of the facial nerve. CT or MRI can be used to confirm the diagnosis.
Treat malignant otitis externa with what type of antibiotics?
SYSTEMIC abx that cover for Pseudomonas. TOPICAL abx are ineffective!
It is important to distinguish between what two differentials when a patient presents with a swollen and painful eye accompanied by fever but has a normal fundoscopy?
Orbital cellulitis (infection of the fat and muscles within the orbit) VS. preseptal cellulitis (infection that involves only the superficial tissues).

Protrusion of the eyeball (proptosis) and decreased visual acuity are usually only seen with orbital cellulitis. CT can be helpful if the clinical presentation is indeterminate or if there is concern for abscess. Treat requires IV broad spectrum ABX.

Note: Cavernous sinus thrombosis sometimes presents similarly to orbital cellulitis but is more often BIlateral with inolvement of cranial nerve III (resulting in ptosis) and V as well as early visual loss. Fudoscopy is usually NOT normal and reveals papilledema and dilated tortuous retinal veins.
Suspect what in a patient with hard to remove white patches in the oral mucosa?
leukoplakia that may lead to squamous cell carcinoma - caused by chronic irritation to the oral mucosa due to smoking, alcohol, or ill-fitting dentures.
Suspect what in a child patient who presents with continued ear drainage for several weeks despite appropriate abx therapy?
cholesteatomas - can be congenital or acquired. Congenital lesions are in pts around the age of 5 or younger. Acquired lesions are due to chronic middle ear disease that leads to formation of a retraction pocket in the tympanic membrane, which can fill with granulation tissue and skin debris. Complications of cholesteatomas include hearing loss, cranial nerve palsies, vertigo, brain abscesses or even meningits. Refer to an otolaryngologist!!
What disease consists of the following features: asthma, chronic rhinosinusitis, nasal polyposis, and bronchospasm or nasal congestion following the ingestion of aspirin or NSAIDs?
Aspirin exacerbated respiratory disease (AERD) - examination will reveal bilat, grey, glistening mucoid masses in the nasal cavities.

Note: food tastes bland secondary to anosmia from nasal congestion.
Suspect what in a patient who presents with severe, sharp headaches, low-grade fever, periorbital edema, and cranial nerve palsies?
cavernous sinus thrombosis (CST) - most are 2dry to a skin infection located in the medial aspect of the face (around eyes and nose) but ethmoid or sphenoid sinusitis can also cause this condition. Headache is usually the most common EARLY symptom, partly due to neuropathic pain from the irritation of V1 and V2 branches of the trigeminal nerve (which explains sharpness and location in the upper face). Cranial nerves III, IV, V1, V2 and VI all pass through the cavernous sinus and can be affected by CST. Low-grade fever and periorbital edema occur several days later due to impaired venous flow in the orbital veins.

Dx with MRI or CT with contrast of the orbits. Tx with IV broad spectrum abx. Sometimes anticoagulation, glucocorticoid therapy or surgery may be needed as well.
Suspect what in a patient who presents with a combination of vertigo, ear fullness, tinnitus, and hearing loss?
Meniere's disease - resulting from distention of the endolymphatic compartment of the inner ear. Episodes of vertigo last 20 min to 24 hours in addition to low frequency, sensorineural hearing loss and tinnitus. Acute symptoms may include vomiting, postural instability, and nystagmus. Triggers that increase endolymphatic retention should be avoided including alcohol, caffeine, nicotine, and high salt foods. A strict, salt restricted diet of 2-3 grams/day is recommended as initial therapy.
What s/sx should lead to suspicion for a diagnosis OTHER than UNcomplicated pharyngitis or tonsillitis?
1) a muffled voice or "hot potato voice"
2) deviation of the uvula
3) prominent UNIlateral lymphadenopathy

This condition is likely peritonsillar abscess and can be fatal! Treatment includes needle aspiration of the peritonsillar abscess and initiation of IV abx.
Dense intramembranous deposits that stain for C3 from a renal biopsy is a characteristic microscopic finding for?
membranoproliferative glomerulonephritis, type 2 - pts present with nephrotic range proteinuria and hematuria. It is caused by IgG antibodies (termed C3 nephritic factor) directed against C3 convertase of the alternative complement pathway.
What are most kidney stones composed of?
75-90% are composed of calcium oxalate (envelope-shaped on microscopy). Small bowel disease, surgical resection or chronic diarrhea can lead to malabsorption of fatty acids. unabsorbed fatty acids chelate calcium --> more oxalic acid free for absorption --> more likely calcium oxalate stones!
Calcium phosphate stones are common in?
primary hyperparathyroidism and renal tubular acidosis.
Uric acid stones (10-15% of renal stones) are common when?
urine is acidic or there is increased cell turnover (hyperuricemia). Dehydration is an important risk factor. Persistent stones due to hyperuricosuria can be treated with purine-restricted diet and allopurinol.
Cysteine stones (< 1% of renal stones) are seen in?
inborn error of metabolism leading to increased excretion of cysteine.
Struvite stones (10-15% of renal stones) are common when?
urine is alkaline bc of infection with urease producing bacteria (e.g. Proteus).
Most common causes of calcium stones?
1) idiopathic hypercalciuria: hypercalciuria, normal SERUM calcium, and absent metabolic dz. *most common form of hypercalciuria.
2) hypercalciuria due to systemic disorders (primary hyperparathyroidism, sarcoidosis)
3) hyperuricosuria
4) hyperoxaluria (due to large amounts of Vit C or green leafy vegetables or 2dry to IBD/short bowel syndrome).
5) Decreased urinary citrate
6) Renal tubular acidosis
7) chronic dz in urine output -- leads to precipitation of calcium salts.
Treatment for calcium oxalate urolithiasis (in order of importance)?
1) increased fluid intake (> 3L per day)
2)normal or increased calcium diet (1000 mg/dL is RDA)
3) dietary sodium restriction (<100 mEq/dL)
4) oxalate restriction (i.e. dark roughage, chocolate, and vitamin C)
5) decreased dietary proteins (i.e. beef, fish, eggs, and poultry.)
Medical treatment for urolithiasis?
Thiazides/amiloride diuretics - decreases urinary calcium excretion (primarily by inducing mild volume depletion which leads to a compensatory rise in proximal reabsorption of sodium and calcium) and prevents the precipitation of calcium in the urine.
What DM drug should be discontinued in patients with acute renal failure, hepatic failure, or sepsis?
Metformin - all increase the chance of developing lactic acidosis

Note: Pioglitazone is contraindicated in liver failure.
Hyperkalemia with significant changes should be rapdily treated with?
calcium gluconate to stabilize the heart cell membranes but effects are short-lived; therefore, agents to reduce the serum concentration of potassium such as insulin and/or sodium polystyrene sulfonate will also be necessary too!
Suspect what in a pt that presents with recurrent episodes of hematuria beginning several days after an upper respiratory infection (serum complement levels are normal)?
IgA nephropathy and post-streptococcal glomerulonephritis are major causes of hematuria after an URI. IgA nephropathy is the MOST common cause in adults and usually occurs less than 5 days after the URI. Post-strep glomerulonephritis averages 10 days after pharyngitis and 21 days for impetigo.
Treatment for overflow incontinence due to diabetic autonomic neuropathy?
Aside from strict glycemic control, intermittent catheterization and cholinergic medications such as bethanechol are options. Heavy alcohol intake may contribute so cessation is important.

Note: pts will have high post-void residual volumes in the bladder.
Suspect what in a patient who presents with palpable purpura, proteinuria, hematuria, and other nonspecific findings such as arthralgias, hepatosplenomegaly, peripheral neuropathy and hypocomplementemia?
Mixed essential cryogloulinemia. Most patients also have hepatitis C.
Two treatment options for end stage renal disease?
dialysis or renal transplantation. Renal transplant is always preferred due to better survival rates and quality of life. A living RELATED donor is best, followed by a living non-related donor and lastly a cadaveric donor.
What qualifies a cystitis infection as complicated?
infections in women who are pregnant, the very young or the very old, diabetics, immunocompromised, or those who have abnormal anatomy of the GU tract.
Management of uncomplicated cystitis?
Urine cultures are not indicated. Oral TMP/SMX and nitrafurantoin are the preferred empiric abx.
Drug that is used to treat serious gram-negative infections but are potentially nephrotoxic?
Aminoglycosides - drug levels and renal function must be monitored closely during therapy.
Suspect what in a young patient that presents with recurrent episodes of hematuria and proteinuria, sensorineural deafness, and a family hx of renal failure?
Alport's syndrome - microscopy shows alternating areas of thinned and thickened capillary loops with splitting of the glomerular basement membrane.
Most common causes of nephrotic syndrome not secondary to a systemic disease are?
minimal change disease, membranous nephropathy, and focal segmental glomerulosclerosis. Minimal change dz is most common in children. The other two are most common in adults, with more than 1/2 of cases in African American patients. FSGS also has an association with obesity, heroin use, and HIV.
Definition of nephrotic syndrome?
heavy proteinuris (> 3g/24 hours), hypoalbuminemia, and peripheral edema.
Pathogenesis of analgesic-induced papillary necrosis?
chronic tubulointerstitial damage - results from papillary ischemia induced by analgesic-mediated vasoconstriction of medullary blood vessels (vasa recta). Sometimes hematuria is prominent, and clots may form causing renal colic.
Peculiar side effect of rifampin?
red to orange discoloration of body fluids including urine, saliva, sweat, and tears.
How to distinguish between the following:
1) chronic bacterial prostatitis
2) inflammatory chronic prostatitis
3) non-inflammatory chronic prostatitis
4) acute bacterial prostatitis
All may present with irritative voiding symptoms.
1) Afebrile pts, normal urinalysis, prostatic secretions show leukocyte count > 10 WBCs/HPF and culture of secretions is POSITIVE.
2) Afebrile pts, normal urinalysis, prostatic secreatons show leukocyte count > 10 WBCs/HPF and culture of secretions is NEGATIVE.
3) Afebrile pts, normal urinalysis, prostatic secretions show a NML number of leukocytes and culture of secretions is NEGATIVE.
4) FEBRILE pt, suprapubic/perineal pain, exquisitely tender prostate is noted on rectal exam, urinalysis shows bacteruria and pyuria.
Tx for dehydration?
IV sodium-containing crystalloid solutions (usually 0.9% NaCl)

Classic signs of dehydration: dry mucosa, marginally high hematocrit and serum electrolytes, BUN/Cr ratio > 20.
Suspect what if a pt with typical renal colic does not show a stone on plain film?
1) radiolucent stone (uric acid stone)
2) calcium stones less than 1-3 mm in diameter
3) non-stone causes (obstruction by a blood clot or tumor)

All will likely show on an ultrasound or CT scan.
Cause and treatment of uric acid stones?
Commonly caused by unusually low urine pH levels (which may be due to a defect in renal ammonia secretion) and hyperuricosuria.

Hydration plus alkalinization of urine to pH > 6.5 with oral potassium bicarbonate or potassium citrate since uric acid stones are highly soluble in alkaline urine.

Also a low-purine diet with/wo allopurinol can be helpful depending on the presence of hyperuricosuria.
First step in management of acute renal failure/kidney injury due to possible urinary retention?
Foley catheterization - it can resolve various post renal obstructions and monitor urine output in prerenal and intrinsic renal failure.

Note: Urine sediment analysis is helpful in differentiating between prerenal and intrinsic renal failure. Muddy brown casts indicate acute tubular nephritis while eosinophilic casts indcate AIN.

IV fluids are critical in prerenal acute kidney injury caused by hypovolemia. In ADEquately hydrated patients with recent-onset oliguria due to prerenal or certain intrinsic renal causes, a loop diuretic to avoid volume overload can be helpful.
Meds commonly known to cause hyperkalemia?
ACE-I, NSAIDs, and potassium-sparing diuretics (such as amiloride and spironolactone).
EKG changes due to hyperkalemia?
early: peaked T waves

followed by prolonged PR interval and QRS duration, and eventual loss of P waves. Progressive widening of the QRS complex and merging with the T wave produces a sine-wave pattern. This can progress to V-fib or asystole.
Management of hyperkalemia?
10 mL of 10% calcium gluconate to stabilize the myocardial membrane WHEN signs of cardiac toxicity are present or potassium level > 6.5. Follow with insulin and/or beta-2 agonists to shift potassium into cells. Sodium bicarbonate can also be used for this purpose.

Slower acting treatments to increase potassium excretion include loop and thiazide diuretics IF renal function of pt is intact.

Dialysis is reserved for those with renal failure and severe life-threatening hyperkalemia unresponsive to conservative measures.
A simple renal cyst should NOT have the following findings:
1) multilocular mass
2) thickened, irregular walls
3) thickened septae within the mass
4) contrast enhancement

simple renal cysts are most common in patients over age 50. They do not require further evaluation.
Suspect what in a male patient with fever, painful enlargement of the testes, and irritative voiding?
acute epididymitis - In younger patients, it is usually caused by sexualy transmitted organisms such as C. trachomatis or N. gonorrhea and is assocated with urethritis (pain at the tip of the penis and urethral discharge). In older men, it is usually non-sexually transmitted and caused by gram negative rods such as E. coli and is associated with a UTI.
Varicoceles that FAIL to empty when a patient is recumbent should always raise suspicion for?
renal cell carcinoma - scrotal varicoceles are usually on the left side and due to obstruction of the gonadal vein where it enters the renal vein.

Most pts with RCC are Asymptomatic until the dz is advanced. Classic triad of flank pain,hematuria, and a palpable abdominal renal mass is uncommon (10% of patients). CT scan of the abdomen is the most sensitive and specific for diagnosing renal cell carcinoma.
Diagnostic procedure of choice for detecting renal stones?
CT withOUT contrast bc it can detect radioopaque (calcium) as well as radiolucent (uric acid) stones.
Dietary recommendations for patients with renal calculi are:
1) DECR dietary protein and oxalate
2) DECR sodium intake
3) INCR fluid intake
4) INCR dietary calcium
Why are patients with nephrotic syndrome at an increased risk for stroke or MI?
because of abnormal lipid metabolism (including elevated LDL and/or a low HDL) as well as intrinsic hypercoagulability (tends to affect the venous more than the arterial system, particularly the renal veins). Both factors lead to accelerated atherosclerosis! Aggressive management including statins or other meds to lower cholesterol is indicated.
It is important to consider what diagnosis in a male patient who presents with symptoms of a UTI?
acute prostatitis because acute CYSTitis is uncommon in men! Pts with prostatitis may also complain of pain in the perineal region and a tender, boggy prostate is often found on PE. Most appropriate next step in order to help direct antibiotic therapy is a mid-stream urine sample. Prostatic massage should be avoided as it can result in bacteremia. Urethral catheterization should be avoided due to inflammation involving the urethra. If urinary retention develops, suprapubic catheterization may be necessary.
When should a diagnosis for membranous glomerulonephritis in a CHILD with nephrotic syndrome be suspected considering minimal change disease is overall the most common cause?
In a pt with active Hepatitis B infection, particularly if the HBeAg is positive (possibly due to deposition of HBeAg itself in the glomeruli).
What should be suspected in a pt that presents with a hx of rheumatoid arthritis, enlarged kidneys, hepatomegaly, generalized edema, and 4+ proteinuria?
Amyloidosis causing nephrotic syndrome. Note that rheumatoid arthritis predisposis to amyloidosis. Renal biopsy will show amyloid deposits that exhibit apple-green birefringence under POLARIZED light after staining with Congo red.
What should be suspected in a patient with a hx of CRF that presents with abnormal hemostasis but normal PT, PTT, and platelet counts?
uremic coagulopathy - BT is reflective of platelet function and is usually prolonged. The platelet count is normal but there is platelet dysfunction that causes bleeding.
Treatment of choice for a uremic coagulopathy?
DDAVP - increases the release of factor VIII:von Willebrand factor multimers from endothelial storage sites. Platelet transfusion is not indicated bc the transfused platelets quickly become inactive.

Note: Major defect in uremic coagulopathies involves platelet-vessel wall and platelet-platelet interactions. Several uremic toxins have been implicated, the chief among which is guanidinosuccinic acid.
Which antidiabetic drug causes some weight loss?
Meformin - assess pt's renal status before starting on metformin
Algorithm for Cushing's disease:
1) 24-hr urinary free cortisol as a screening test - 90% of patients will have values greater than 90 microgram/24 hr.

2) Low dose dexamethasone test can also be used as a screening test - in patients wo any pathology, ACTH levels should decrease whereas in Cushing's, ACTH levels remain high.

3) Once a screening test is positive, plasma ACTH levels determine the etiology of the syndrome. Plasma ACTH levels > 20 pg/mL can occur in Cushing's and ectopic ACTH production.

4) High-dose dexamethasone suppression test can distinguish btn Cushing's and ectopic ACTH production. In Cushing's, the 24-hr urinary cortisol or serum cortisol levels will decrease by 50% of basal cortisol levels. NO suppression indicates ectopic ACTH prodxn.

This is explained by the fact that excess ACTH secretion from pituitary adenomas are only relatively resistant to negative feedback whereas most ectopic tumors are completely resistant to feedback inhibition.

Also, RAPD develoment of symptoms (hypokalemic alkalosis, pigmentation, and hypertension) is more indicative of ectopic secretion.
Management of diabetic gastroparesis includes:
1) improved glycemic control (delayed gastric emptying makes this difficult to achieve, often leading to post-meal hypOglycemia after insulin injection.
2) Small, frequent meals
3) Dopamine antagonists (e.g. metoclopramide, domperidone) before meals.
4) Bethanechol
5) Erythromycin - this drug interacts with motilin receptors and can promote gastric emptying
6) Cisapride - available only through manufacturer after documentation of need for drug and thorough assessment of the individual's risk factors for cardiac arrhythmia.
How does diabetic autonomic neuropathy of the GI tract manifest?
1) stomach involvment leads to gastroparesis with anorexia, n/v, abdominal bloating, and early satiety
2) small intestine involvement causes diarrhea due to bacterial overgrowth
3) large intestine involvement presents with constipation.
What is megestrol acetate used for?
anorexia associated with cancer
How to detect factitious thyrotoxicosis?
Signs/symptoms of hyperthyroidism but NO goiter or exophthalmos. Low TSH and elevated T3/T4. 24-hr radioiodine uptake test shows diffusely decreased iodine uptake by the thyroid. Biopsy shows follicular atrophy.
What causes hypertension in hyperthyroid states?
caused by hyperdynamic circulation - predominantly systolic hypertension and an increase in pulse pressure
What causes hypertension in hypOthyroid states?
increased systemic vascular resistance - predeominantly diastolic htn
Indications for parathyroidectomy?
Needed for all SYMPTOMATIC patients with primary hyperparathyroidism.

Criterion for ASYMPtomatic patients with primary hyperparathyroidism are:
1) serum calcium at least 1 mg/dL above the upper limit of normal
2) young age (< 50 years old)
3) bone mineral density less than T-2.5 at any site.
4) Reduced renal function.
What two differentials should be considered when lab results show hypercalcemia, hypophosphatemia, and inappropriately elevated PTH levels?
primary hyperparathyroidism and familial hypocalciuric hypercalcemia.

24-hr urinary calcium test helps distinguish the two. Levels > 200 mg indicate primary hyperparathyroidism while levels < 100 mg indicate the latter.
What is a sestambi scan?
Surgeons use it to assess and localize parathyroid adenomas for guidance to surgical approach.
Why is corrected calcium important?
It takes hypoalbuminemia into account. Albumin plays an important role in homeostasis of the 3 forms of calcium: ionized (active) form 45%, albumin-bound 40%, and bound to inorganic/organic anions 15%. Pts with low albumin may have low TOTAL plasma calcium but normal levels of ionized calcium therefore remain healthy.

For every 1 g/dL change in serum albumin from 4 g/dL, total calcium should be expected to decrease by 0.8 mg/dL.
Most prominent cause of primary adrenal insufficiency in developING countries?
adrenal tuberculosis - also, CT scan often shows calcification of both adrenal glands. tx is lifelong replacement with glucocorticoids and mineralocorticoids.
Most prominent cause of primary adrenal insufficiency in developED countries?
autoimmune adrenalitis (more than 80% of patients with primary adrenal insufficiency)
What is cosyntropin?
synthetic ACTH - should cause a rise in serum cortisol
Two etiologies of early morning hypERglycemia?
1) inadequate insulin dosage
2) Somogyi effect

Measurement of 3AM blood glucose is helpful in distinguishing the two. 3AM hypOglycemia will cause an incease in levels of counterregulatory hormones (i.e. epinephrine, norepinephrine, glucagon), which consequently increase the rate of glycogenolysis and gluconeogenesis. This eventually cuases elevation of the morning blood glucose level.
Lab values that confirm a diagnosis of SIADH?
low PLASMA osmolality (<280 mOsm/kg) with high URINE osmolality (>100-150 mOsm/Kg).

These patients are characterized by hypOtonic (i.e. low PLASMA osmolarity) hopOnatremia with euvolemia due to persistently elevated ADH levels in the absence of appropriate stimuli for vasopressin release.

Note: one cause for SIADH is NSAID therapy
First line treatment for micro- versus macroprolactinomas?
Medical treatment for both bc it not only results in normalization of prolactin levels but also significant reduction in tumor size! Use dopaminergic agents such as bromocriptine and cabergoline. Cabergoline is a new drug with fewer side effects.
Definition of a microprolactinoma?
less than 10 mm in diameter - manifests as amenorrhea and galactorrhea in women and hypogonadism in males. Usually does not cause problems with other pituitary hormones or a mass effect.
TSH-secreting pituitary adenomas lead to...
excess TSH levels which stimulate thyroid gland. Elevated circulating thyroid hormone levels with inappropriately normal/elevated TSH levls is characteristic.

Note: pathophysiology generally involves the overproduction of the ALPHA-subunit of TSH.
Most appropriate initial management of DKA?
rapid IV administration of normal saline and REGular insulin.

Note: bicarb administration is usually NOT indicated due to adverse effects.
Criteria to make diagnosis of DKA?
1) blood glucose > 250
2) pH < 7.3 or low serum bicarb < 15-20 mmol/L
3) detection of plasma ketones
Most common risk factor for foot ulcerations?
Diabetic neuropathy (seen in 80% of diabetics with foot ulcers) - even more than peripheral vascular disease and smoking.
Suspect what in a patient with decreased hearing, increased hat size, and increased alk phos levels?
Paget's disease - pt is usually over 40 years. Often asymptomatic but when symptomatic, first symptom is crainial enlargement, associated hearing loss, and occasional headaches.
Basic pathophysiologic mechanism in Paget dz?
abnormal bone remodeling -excess osteoclastic bone resorption with increased numbers of larger than normal osteoclasts at the involved sites --> compensatory activation of the osteoblasts --> immature bone deposition with transformation of normal lamellar and woven bone into a chaotic "mosaic" pattern
What labs can accurately reflect the extent and activity of Paget's dz?
1) alkaline phosphatase - marker of bone formation - used to assess the activity of disease as well as response to treatment
2) urinary n telopeptide - most commonly used as a marker of bone resorption
2)
Pathogenesis of osteomalacia?
Vitamin D deficiency --> decreased intestinal calcium and phosphorus absorption --> hypocalcemia stimulates parathyroid glands --> 2dry hyperparathyroidism brings the serum calcium levels to normal or near normal BUT increases urinary phosphate excretion

Note: Look for greater hypophosphatemia than hypocalcemia, especially in the early stages of osteomalacia
Differential diagnosis of NORMOtensive patients with hypokalemia and metabolic alkalosis includes?
1) diuretic use
2) surreptitious vomiting
3) Bartter syndrome
4) Gitelman syndrome

Clue: Urine chloride level is MARKEDLY elevated (> 20 mEq/L and most often >40 mEq/L) in Bartter and Gitelman syndromes.
Classic presentation of Bartter syndrome?
polyuria, polydipsia, and growht and mental retardation that presents early in life but can occur later in life too.

Defect is in sodium and chloride reabsorption in the thick ASCENDing limb of the LOH, resulting in hypovolemia and consequent activation of the renin-angiotensin aldosterone system (RAAS). Activated RAAS causes an incr in potassium and hydrogen ion secretion, leading to hypokalemia and metabolic alkalosis. Sodium tends to be normal!

Note: Gitelman syndrome is a subset of Bartter syndrome with a defect in the distal convoluted tubule causing the same sequence of events.
Most common cause of hypokalemia?
diuretic use - can be diffeicult to identify
How to distinguish between primary hyperaldosteronism and renin-secreting tumors, both of which are characterized by HTN?
Plasma renin activity - HIGH in renin-secreting tumors and low in primary hyperaldosteronism. Plasma aldosterone will be high in BOTH conditions. Serum sodium tends to be high in both conditions too.
Preferred treatment for Graves disease and the contraindications of treatment?
Radioactive iodine ablative therapy - most patients achieve euthyroidism with a single dose of radioactive iodine. Approx 10-30% will become hypOthyroid during first 2 years and 5% per year therafter. Usual time for initial improvement is 6-8 weeks after administration of radioactive iodine

Contraindications: pregnancy and very severe ophthalmopathy.
Suspect what in a patient that presents with hypertension, muscle weakness, and numbness?
Primary hyperaldosteronism - usually (85% of pts) caused by an aldosterone-secreting adrenal tumor. The rest have adrenal hyperplasia. Excess aldosterone in the body causes increased renal sodium reabsorption with resultant hypertension. Aldosterone also increases renal potassium loss with resultant MUSCLE weakness/numbness.
Most specific lab value that indicates primary hyperaldosteronism?
increased early morning aldosterone/renin ratio (>30) bc increased aldosterone suppresses renin.
American Diabetes Association guidelines for the diagnosis of diabetes mellitus?
Any 1 of the following:
1) HbA1C - over 6.5%
2) fasting plasma glucose over 125 mg/dl
3) plasma glucose > 200 mg/dl after 2 hours into a 75 g glucose tolerance test
4) random plasma glucose > 200 mg/dL

Note: all tests should be repeated bc false positives are high. Recommended that repeat testing be performed using the SAME screening test that was initially abnormal.
Management of non-ketotic hyperglycemia?
First and most important step is fluid replacement with NORMAL saline. Because of large volumes of glucose induced osmotic diuresis, pateints may require up to 8-10 L of normal saline to reach a euvolemic state. Normal saline can then be changed to half-normal saline.

Regular insulin should be administered.

Potassium should be administered in ALL cases once potassium reaches to the normal level. This is due to potential for hypOkalemia as K+ moves into the cells with administered insulin.

5% dextrse is given once blood glucose level has been lowered to 250 mg/dl by insulin therapy to prevent the development of cerebral edema.
Manifestations of hypercalcemia of malignancy due to prodxn of PTH related peptide?
Same effects that are seen with PTH secretion - including increased bone resorption, increased renal tubular calcium reabsorption, and phosphate secretion.
Suspect what in a patient that presents with symptoms of hypothyroidism despite elevated T3/T4 levels and a normal to elevated TSH level?
generalized resistance to thyroid hormones from receptor defects on the peripheral tissue. Patients usually present at an early age with growth and mental retardation; however pts with milder defects can present later in life.
What is sick euthyroid syndrome?
'Low T3 sydnrome' - any pt with an acute, severe, systemic illness may have abnormal thyroid function tests during the illness and while recovering from the illness. This is why TFTs are generally not performed unless there is a strong indication.

This condition is thought to be due to caloric deprivation and an increase in cytokine levels. Most common pattern is a fall in TOTAL and free T3 levels due to decreased peipheral conversion from T4 to T3. There is a rough correlation btn the severity of the underlying dz and fall in T3 levels. If illness continues for an extended period of time, serum T4 and TSH levels also decrease.

On recovery from non-thyroidal illness, pts often experience a modest, transient increase in serum TSH level, which is often misinterpreted as subclinical hypothyroidism.
Indications for treatment of Paget's disease:
1) bone pain
2) hypercalcemia of immobilization
3) neuro deficit
4) high output cardiac failure
5) preparation for orthopedic surgery
6) involvement of weight-bearing bones (to prevent deformities)

The initial goal is to establish which bones have been affected. Can be ascertained by full body bone scan, followed by radiologic confirmation in the documented areas of increased tracer uptake.

Symptomatic patients are best treated with oral or IV bisphosphonates. Calcium and vitamin D has NO effect on Paget's disease.
MEN II consists of?
1) virtually 100% will have C-cell hyperplasia or medullary thyroid carcinoma
2) 50% will have pheochrmocytoma
3) 20-30% have hyperparathyroidism
Best next step in a pt with suspected pheochromocytoma plus elevated serum calcium?
check serum calcitonin levels for possible medullary thyroid cancer (MEN II)
When is ACE-I therapy indicated in a diabetic?
when the patient has microalbuminuria, even if the blood pressure is normal. Microalbuminuria is a sensitive marker of renal microvascular damage.
Most helpful diagnostic test in a pt with suspected erectile dysfunction?
nocturnal penile tumescence - helps differentiate a psychogenic causes (these patients are eugonadal and still experience spontaneous erections during REM sleep and on waking up) VS. organic causes.
In patients with suspected MEN II syndrome, what is the recommended screening test?
genetic testing has replaced biochemical measurement of serum calcitonin. If genetic analysis is positive for a RET proto-oncogene (more than 95% of pts with MEN II have this mutation), total thyroidectomy is indicated.
What lab values can be expected in X-linked hypophosphatemic rickets?
Low serum phosphate due to RENAL phosphate wasting. There may also be a defect in 1-hydroxylase and as a result 1,25- dihydroxy vitamin D (calcitriol) may be low.

Serum calcium, PTH, alk phos, and 25-hydroxy vitamin D are all normal.
What lab values can be expected in psuedohypoparathyroidism?
low serum calcium, high serum phosphate, and high serum PTH. Alk phos and Vit D levels are WNL.
What effects on calcium metabolism, phophate, PTH, and vitamin D does renal failure have?
low serum calcium, high serum phophate, high PTH, and low 1,25 dihydroxy vitamin D.
Osteomalacia due to Vitamin D deficiency shows what lab values?
LOW 25-OH Vitamin D, low calcium, low phosphate, high PTH (secondary hyperparathyrodisim). 2dry increase in PTH brings calcium closer to normal values but makes hypophosphatemia worse.
What lab value indicates that microalbuminuria has progressed to macroproteinuria?
urine protein excretion of more than 300 mg/d - this is accompanied by progressive decline in GFR. Intensive blood pressure control is the most beneficial therapy to slow progression of diabetic nephropathy.
Immediate cessation of antithyroid drugs (propilthiouracil or methimazole) is indicated when?
any pt taking antithyroid drugs develops fever and sore throat suspicious of agranulocytosis caused by immune destruction of granulocytes (most cases occur wi 90 days of treatment). After stopping drug, measure WBC count. WBC < 1,000/cubic mm warrants permanent discontinuation whereas WBC count > 1,500/cubic mm makes antithyroid drug toxicity the unlikely source of fever/sore throat.
How does PARTIAL deficiency of 21-hydroxylase present?
in ADULThood as hyperandrogenism but NO salt wasting (therefore normal blood pressure).
What is the next best step in a male pt with suscpected secondary (central) hypogonadism indicated by low testosterone and low or INNAPPOPriately normal levels of gonadatropin levels?
prolactin levels - high serum prolactin inhibits release of GnRH thereby resulting in hypogonadism.
glycosylated hemoglobin is an excellent way to monitor CHRONIC glycemic control bc?
it is reflective of the pt's average glucose levels over the preceding 100-120 days (which correlates with RBC survival time). Generally a 1% increase in HbA1c corresponds with a 35 mg/dL increase in the mean plasma glucose level.
The most reliable indicator of metabolic recovery in a pt with diabetic ketoacidosis?
serum anion gap or arterial pH
Drugs of choice in diabetic neuropathy?
tricyclic antidepressants BUT TCAs can worsen urinary symptoms (due to cystopathy) and orthostatic hypotension (due to cardiovascular autonomic neuropathy). Gabapentin is an alternative for these patients.
Pathophysiologic mechanism of Addison's disease?
autoimmune! aka autoimmune adrenalitis. Pts with autoimmune adrenalitis also have autoimmune damage of other endocrine glands such as thyroid, parathyroid, and ovaries. Other non-endocrine autoimmune conditions such as pernicious anemia and vitiligo are also common.
How should patients with PID be managed?
1) Appropriate abx (ceftriaxone for gonorrhea and azithromycin for chlamydia)
2) Counseled on safe sex practices
3) encouraged to inform sexual partners in the past 60 days of their condition
4) Screened for HIV, syphillis, hepatitis B, cervical cancer (pap smear), and (if they have a hx of IV drug abuse) hepatitis C.
A PPD test is positive when?
1) induration > 5 mm in:
HIV-positive pts, with recent TB contact, signs of TB on CXR, or immunosuppressed.

2) Induration > 10 mm in:
Recent immigrants, IV drug abusers, exposure to high-risk settings (prisons, homeless shelters), or hx of DM or chronic kidney disease or malignancy or fibrotic lung disease.

Also children less than 4 years or teens exposed to high risk adults.

3) induration > 15 in:
healthy individuals with no risk factors
Treatment for a positive PPD test?
Isoniazid for chemoprophylaxis for 9 months PLUS pyridoxine to prevent isoniazid-induced neuropathy.

Isoniazid-induced hepatitis is still possible, so check LFTs periodically.
What is the gardener's disease?
Sporotrichosis from Sporothrix schenckii - initial lesion is a reddish nodule that later ulcerates, at the site of the thorn pick or skin injury. From this site of inoculation, the fungus spreads along lymphatics forming subQ nodules and ulcers.
Esophagitis in HIV usually occurs when the CD4 count is?
< 50/microL. Pts complain of swalloing and substernal burning. The most common agent is Candida. Start treating with oral fuconazole for 3-5 days. Failure to respond warrants further investigation with endoscopy, biopsy, and culture.
How to distinguish between a primary HIV infection and infectious mononucleosis?
1) Rash (unless antibiotics have been administered) and diarrhea are less likely in infectious mono.

2) Tonsillar exudates are uncommon in HIV.
What is Kaposi sarcoma?
Cutaneous lesions caused by human hersvirus 8 - lesions begin as papules and later develop into plaques or nodules. The color typically changes from light brown to violet. No associated necrosis of the skin or underlying structures.
Management of a healthcare worker that is exposed to HIV?
HIV serology and immediate initiation of aniretroviral therapy with 2-3 drugs.
Management of mucormycosis most often caused by the fungus, Rhizopus?
aggressive surgical debridement plus early systemic chemotherapy with amphotericin B.
Management of disseminated histoplasmosis in HIV pts?
Initial treatment with IV amphotericin B decreases the fungal load, and lifelong treatment with itraconazole prevents relapse.
Classic signs of secondary syphillis?
Bilateral symmetrical maculopapular rash involving the entire trunk and extremities (including palms and soles)! Also condylomata lata - broad exophythic formations which develop on the anogenital region or upper thighs and ulcerate subsequently. sSecond stage lesions may resolve spontaeously or even, never appear.
What is indicated in a pt suspected to have infectious mononucleosis with a negative heterophile test?
EBV-specific antibody test
Treatment for primary syphillis in a penicillin allergic patient?
single dose of oral azithromycin or a 2-week course of doxycycline
Treatment of Pneumocystis pneumonia (an AIDS defining illness when CD4 counts are < 200)?
TMP-SMX is the DOC.

Add oral prednisolone when PaO2 < 70 mmHg.
Clinical features of Pneumocystis pneumonia?
fever, DRY cough, exertional dyspnea, imaging that shows diffuse bilat intersititial infiltrates.
Most likely organism in osteomyelitis from a nail puncture wound?
Pseudomonas aeruginosa - treat with oral or parenteral quinolones and aggressive surgical debridement
What should be considered in the differential when a pt with mononucleosis-like symptoms and atypical lymphocytes have a negative monospot test?
CMV - usually presents withOUT pharyngitis and lymphadenopathy unlike EBV.
Suspect what organism with nausea and vomiting 1-6 hours after eating rice?
Bacillus cereus - from a PREformed, heat stable toxin.
Most common cause of pneumonia in HIV pts?
encapsulated bacteriadue to impaired humoral immunity, especially Pneumococcus
Streptococcus bovis endocarditis whould prompt investigation for?
colorectal or upper GI cancer
A tick bite infection that is indemic to the northeastern United States and causes hemolyis?
Babesiosis caused by Babesia. Unlike other tick-borne illnesses, rash is NOT a feature except in severe infection with thrombocytopenia which may cause a secondary petechial or purpuric rash.

Dx is made from Giemsa-stained blood smear. Tx is with either quinine-clindamycin OR atovaquone-azithromycin.
The characteristic rash of rubella starts where?
On the FACE and progresses to trunk and extremities. Prodromal symptoms include fever and occipital/posterior cervical lymphadenopathy. Adult women usually have associated arthritis!

Note: these patients usually have an unknown or not up to date vaccination status.

Also, measles (rubeola) can present with a similar rash that starts on the face but will have Koplik's spots and NO arthritis.
Most appropriate management for a pt suspected to have HSV encephalitis?
PCR for herpes simplex virus DNA from a CSF sample (not viral culture!). Start IV acyclovir without delay!
When can influenza virus be treated with more than bed rest and simple analgesics such as acetaminophen?
Antivirals are only effective within 48 hours of onset of illness.

Influenza A - amantadine and rimantadine

Influenza A & B - neuraminidase inhibitors zanamivir or oseltamivir are effective.

Note: treatment with antivirals shortens duration of symptoms by 2-3 days. Typical duration is usually 1-7 days. Most common in the fall and winter months.
Treatment of choice for CNS cryptococcal infection in AIDS pt?
IV amphotericin plus flucytosine.

Note: Cryptococcus grows as an "encapsulated" yeast on CSF cultures.
What can cause pulmonary cavitation in an HIV-infected patient?
many organisms: Mycobacterium tuberculosis, atypical mycobacteria, Nocardia, gram-negative rods, and anaerobes.
How to diagnose Nocardia related pulmonary cavitation if suspected?
A presumptive diagnosis can be made if sputum exam shows partially acid-fast, filamentous, branching rods.

DOC is TMP-SMX.

The lung is the most frequently involved organ and infection can manifest as nodules, reticulonodular pattern, diffuse pulmonary infiltrate, abscess, or cavity formation.
When should Doxycycline be avoided as first-line treatment for early Lyme disease and possible simultaneous ehrlichiosis (spread by the same vector)?
Children and pregnant/lactating mothers bc of possible skeletal and dental problems.

Amoxicillin is the preferred tx in these cases.
What other organ beside the liver (hydatid cysts) is commonly affected by echinococcosis?
lungs in 25% - transmitted in areas with sheep and dogs.
Poorly controlled diabetes predisposes patients to _______ which causes a bloody, necrotic infection of the nasal cavities and often involves chemosis, proptosis, and diplopia of the eyes?
mucormycosis caused by Rhizopus.
HIV pts should be on MAC prophylaxis at what point?
CD4 < 50/microL
How is disseminated histoplasmosis (occurs in immunocompromised pts) characterized?
Non-specific symptoms plus pancytopenia, hepatosplenomegaly, and PALATAL ulcers.
Suspect what in an AIDS pt with multiple ring-enhancing lesions on CT of the CNS?
toxoplasmosis - TMP-SMX for prophylaxis and empirical sulfadiazine and pyrimethamine is BOTH diagnostic and therapeutic.
Suspect what with a bright red, firm, friable, exophytic nodule in an HIV pt?
Bacillary angiomatosis caused by Bartonella - oral erythromycin is the ABX of choice.
Definition of febrile neutropenia?
absolute neutrophil count < 1500/microL PLUS a single temp reading of 100.9 OR a sustained temp of 100.4 for over an hour.

This is a medical emergency! Cover for Pseudomonas aeruginosa and treat with monotherapy or combination therapy!

monotherapy: cefepime, ceftazidime, imipenem, or meropenem.

Combo therapy: aminoglycoside plus an anti-pseudomonal beta-lactam.
What form of MS is characterized by well-defined acute episodes with NO significant disease progression btn episodes.
relapsing-remitting form of MS - several well defined clinical trials have proven that INTERFERON-BETA decreases the frequency of relapse and reduces disability in pts with relapsing-remitting form of MS.
An important complication of subarachnoid hemorrhage?
hyponatremia from "cerebral salt-wasting syndrome" - pathology involves (1) inappropriate secretion of vasopressin, which causes wter retention and (2) an increased secretion of atrial/brain natriuretic peptide, which causes cerebral salt wasting. Resolves wi 1-2 weeks.

Any intracranial hemorrhage can also cause SIADH leading to hyponatremia. Tx is water restriction.
Classic triad of normal pressure hydrocephalus?
abnormal gait, incontinence, and dementia - due to increased VENTRICULAR size withOUT persistent elevations in intracranial pressure.
Pathophysiology of normal pressure hydrocephalus?
TRANSIENT increase in intracranial pressure that causes ventricular enlargement. After ventricles enlarge, the pressure returns to normal. Initial increase in pressure is due to DIMINished CSF absorption at the arachnoid villi OR obstructive hydrocephalus.
Features of NML age-related cognitive changes?
tiredness, occasional forgetfulness, occasional word finding difficulty, and trouble falling asleep. Dementia canNOT be diagnosed unless there are functional impairments!
Best way to determine if a Guillain-Barry patient is at high-risk for developing respiratory failure?
SERIAL measurements of bedside vital capacity. VC below 15 mL/kg, especially with a clear downward trend indicates a significantly INCR risk for ventilatory failure.

Note: 20-30% will develop respiratory failure.
Antecedent to Guillain-Barre?
respiratory tract or GI (especially with Campylobacter infection) infection.
What is internuclear ophthalmoplegia?
A disorder of conjugate lateral gaze - eye shows impairment of ADDuction during gaze to the CONTRAlateral side. The opposite (contralateral) eye ABducts but with nystagumus. Same thing happens when gaze is changed to the other direction.

Convergence remains intact. Due to dysfunction in the MEDIAL LONGITUDINAL FASCICULUS, a characteristic finding in multiple sclerosis.
Exacerbationof neuro deficits by hot weather or exercise are a useful clue to what dx?
MS
Suspect what in a pt with rapid onset of severe pain and vision impairment with an effected that appears injected with a NON-reactive DILated pupil?
acute angle closure glaucoma - when a preexisting narrow anterior chamber angle is closed in response to pupillary dilation from medications (anticholinergics or sympathomimetics) or other stimuli (such as dime light). If untreated, can lead to severe and permanent vision loss in 2-5 hours after onset.
Typical presenting features of Huntington's?
mood disturbances (depression, apathy), dementia, anc chorea (facial grimacing, ataxia, dystonia, tongue protrusion, writhing movements of the extremities), and a family hx of similar symptoms.

Note: affects BOTH sexes equally. Age of presentation typically btn 30-50 years.
Approved treatment for amyotrophic lateral sclerosis that prolongs survival and time to tracheostomy?
riluzole - a glutamate inhibitor. Does not arrest underlying pathological process.

note: this is a neurodegenerative disorder NOT immunologically-mediated so corticosteroids and IVIG have no role in mgmt.
Most appropriate management for pt suspected to have an acute ISCHEMIC stroke?
1) First a NON-contrast head CT to confirm that stroke is ischemic and not hemorrhagic.
2) Confirmed ischemic stroke should be treated with fibrinolytics such as intravenous alteplase (tPA) within 3-4.5 hours of symptom onset.

Note: Anticoagulation with heparin is not recommended for acute ischemic stroke even if etiology is CARDIOembolic bc of increased risk for intracranial hemorrhage. However, warfarin anticoagulation should be started 2 wks after an acute CARDIOembolic stroke to prevent recurrence.
Pronator drift is a relatively sensitive and specific physical exam finding for?
upper motor neuron damage affecting the upper extremities. The supinator muscles are naturally weaker than the pronators so when pts close their eyes with arm extension and palms facing upward, an AFFECTED arm will tend to pronate. However, a pt that is faking will "drop" the affected arm withOUT pronating. Pt with strokes my demonstrate pronator drift.
Hemi-neglect syndrome affects what part of the brain?
the NON-dominant (usually right side) PARIETAL lobe, which is responsible for spatial organization.
Manifestation of a lesion to the POSTERIOR limb of internal capsule (typically from a lacunar infarct)?
UNIlateral motor hemiparesis of the face, arm, and leg withOUT loss of higher cortical function and NO visual field abnormalities.
Manifestation of middle cerebral artery occlusion?
CONTRAlateral hemiplegia, conjugate eye deviation TOWARD side of injury, and homonoymous hemianopia. Aphasia if the DOMinant hemisphere is involved OR hemi-neglect if the NON-dominant side is involved.
Manifestation of anterior cerebral artery occlusion?
CONTRAlateral weakness that affects predominantly lower extremities.
Manifestation of a lesion to the vertebrobasilar system (supplying the brain stem)?
"alternate" syndrome - CONTRAlateral hemiplegia BUT IPSIlateral cranial nerve involvement.
Suspect what in a pt that presents with Parkinsonism symptoms, plus orthostatic hypotension, impotence, incontinence, or other autonomic symptoms?
Shy-Drager syndrome aka multiple system atrophy, a degenerative dz characterized by:
1) Parkinsonism
2) Autonomic dysfunction (postural hypotension, abnormal sweating, bowl or bladder dysfunction, abnormal salivation/lacrimation, impotence, gastroparesis, etc.)
3) Widespread neuro deficits (cerebellar, pyramidal or lower motor neuron).

Note: Anti-Parkinson drugs are INeffective. Tx is aimed at intravascular volume expansion with fudrocortisone, salt supplements, alpha-adrenergic agonists, and application of contrictive garments to the lower body.
How is Riley-Day syndrome aka familial dysautonomia characterized?
seen predominantly in Ashkenazi Jewish children - gross dysfunction of the autonomic nervous system with severe orthostatic hypotension.
How doesa thalamic stroke present?
aka Dejerine-Roussy syndrome - caused by a stroke involving the ventral postero-lateral (VPL) nucleus of the thalamus, which ransmits sensory information from the contralateral side of the body.

Classic presentatin involves CONTRAlateral hemiANESthesia with accompanied TRANSient hemiparesis, athetosis, or ballistic movements. Severe DYSESTHesia (hypersensitivity to all kinds of stimuli inducing severe pain) of the affected area is also typical.
Most common causative organisms of brain abscesses?
aerobic and ANaerobic streptococci and Bacteroides species (ANaerobe).
An ISOLATED, round, smooth-bordered, ring-enhancing intracranial lesion on contrast CT scan of the brain in an immunoCOMPETENT pt is suspicious for?
brain abscess especially if there is a known extracranial infection. Streptococcus and Bacteroides (anaerobe) are the most common causes.
Suspect what in a pt with cafe-au-lait spots, axillary freckles, Lisch nodules of the iris, neurofibromas, and bony lesions?
Type 1 neurofibroma.

Note: Neurofibromatosis is a neurocutaneous syndrome with a tendency to form tumors in the CNS, PNS, skin and viscera.
Suspect what in a pt with brain tumors, especially bilateral acoustic neuromas?
Type 2 neurofibramatosis.

Note: Neurofibromatosis is a neurocutaneous syndrome with a tendency to form tumors in the CNS, PNS, skin and viscera.
Suspect what in a pt with ash leaf hypOpigmentation, cardiac rhabdomyomas, kidney angioleimyomas, mental retardation, and seizures?
Tuberous sclerosis: a neurocutaneous syndrome
Suspect what in a pt with port wine stains in the V1 cranial nerve distribution, angomatous malformations of the brain, seizures, and hemiparesis?
Sturge-Weber syndrome: a neurocutaneous syndrome
CSF analysis reveals what findings in Guillain-Barre?
INCR protein with remaining factors being NML (including glucose levels, WBC, and RBC counts).
How does anticholinergic excess present?
Red as a beet, dry as a bone, hot as a hare, blind as a bat, mad as a hater, and full as a flask which describes:
flushing, anhidrosis/dry mouth, hyperthermia, mydriasis/vision changes, delirium/confusion, and urinary retention/constipation.

Headache, dizziness and tachycardia can also be present: headache and retro-orbital pain is attributed to precipitation of acute glaucoma by anticholinergics!!!!!!

ex of anticholinergics: trihexyphenidyl, benztropine
Suspect what in a pt with hx of INTERmittent, painLESS vision loss (lasting a few seconds) with no other complaints and no hx of trauma to the eye BUT a medical hx significant for cardiac risk factors?
Amaurosis fugax - painLESS loss of vision from emboli, which is a warning sign for impending stroke. Most emobli occur from the carotid bifurcation. Hence a duplex ultrasound of the neck is often done to identify plaques that may be present.
Suspect what in a pt that presents with inability to move one-half of the face for 24 hours and absence of forehead furrows?
Bell's palsy (peripheral 7th nerve palsy). A central facial paresis can be ruled out bc patients with central lesions STILL HAVE forehead furrows due to intact contralateral MOTOR innervation.

So forehead muscles SHOULD be paralyzed in Bell's palsy whereas the forehead muscles are not paralyzed in a central lesion.
Suspect what type of lesion with a patient that has Broca's aphasia with right-sided weakness?
a left MCA infarct of the FRONTAL lobe, likely from a CARDIAC embolic source!

Note: Broca's area is in the left frontal lobe.
Hallmarks of Parkinson dz?
mask-like immobile facial expression, bradykinesia, resting tremor, rigidity and a festinating gait. Thee is general slowing of all motor activity (hypokinetic gait) so pt will take short, NARROW-based, shuffling steps.
Waddling gait indicates?
muscular dystrophy (owing to weakness of gluteal muscles).
spastic gait indicates?
lesions of the upper motor neuron (e.g. spinal cord injury or cerebral palsy).
gait disequilibirim indicates?
disorders of the frontal lobe and multiple sensory systems
WIDE-based, high-stepping gait?
loss of proprioception

clue: Romberg's sign may be positive (i.e. the pt sways on standing with his feet together and eyes closed)
en-bloc gait indicates?
vestibular ataxia - a staggering gait with minimal head movements during walking plus vertigo and nystagmus.
Difference between dizziness and vertigo?
dizziness - sensation of imbalance and unsteadiness

vertigo - illusionary feeling of head movement frequently described as "head spinning"
common cause of vertigo?
acute labyrinnthine dysfunction aka "acute labyrinthitis" or "vestibular neuritis." The etiology is not found in most instances.

another important cuase is benign paroxysmal positional vertigo (BPPV), where the symptoms are precipitated by recumbent head position. About 30% of cases after head trauma, but typically no cause is found.
Difference btn subural and epidural hematoma?
subdural - ruptue of bridging veins that is semi-LETNICULAR in shape on CT - usually due to severe trauma or MINOR trauma in pts on anticoagulation therapy. More common in the elderly and alcoholics.

epidural hematoma - results from rupture of the middle meningeal artery with a bioCONVEX shape on CT - results from trauma
Four cardinal symptoms of RLS:
1) An uncomfortable sensation or urge to move the legs
2) discomfort that worsens in the evening or during sleep
3) discomfort which worsens at rest, and
4) discomfort alleviated by movement of the affected limb

Also tends to improve after massage or warming. More common in middle-age to older pts and in those with chronic kidney dz and/or iron deficiency anemia. Mechanism may involve abnormalities of dopaminergic transmission therefore dopamine agonists (pramiprexole, ropinerole, or levadopa) can help reduce symptoms and improve sleep quality.
Some broad generalizations for CNS lesions:
brainSTEM lesions - involve cranial nerves and sensory loss of 1/2 of the face and the CONTRAlateral half of the body.

thalamic and cortical lesions - sensory loss of 1/2 of the face and the SAME half of the body.
Medial medullary syndrome is typically associated with?
CONTRAlateral SPASTIC hemiplegia, CONTRAlateral vibratory/proprioception loss, and tongue deviation TOWARD the injured side.
Wallenberg syndrome?
lesion to the lateral medulla - IPSIlateral Horner syndrome, loss of pain and temperature to the face; weakness of the palate, pharynx, and vocal cords, cerebellar ataxia, and loss of pain and temp to the CONTRAlateral body.
Most common sites for spontaneous intracranial hemorrhage (usually caused by HTN)?
BASAL GANGLIA, cerebellum, thalamus, and pons.
What should be screened for in all patients diagnosed with myasthenia gravis?
coexisting thymoma (present in ~15%) via CT of the chest.
Sometimes difficult to distingush between myasthenia gravis and amyotrophic lateral sclerosis, what physical exam finding can be helpful?
normal reflexes are more suggestive of MG.
One of the most specific symptoms indicating dementia?
impaired activities of daily functioning
Typical CT/MRI findings in the high-grade astrocytoma of glioblastoma mulitforme?
HETEROgenous and serpiginous (slowly creeping/spreading with wavy border) contrast enhancement.

Classic "butterfly" appearance with central necrosis for GBM.
Suspect what when a pt presents with s/sx of ONLY upper motor neuron dysfunction (including weakness, hyperreflexia, and extensor plantar response) especially if limited to the lower extremities?
indicates a CNS lesion - since bilat and limited to lower extremities, lesion can be localized to the spinal cord. (Dysfunction is always distal to the site of spinal cord involvement). Possible etiologies include disk herniation, abscess, trauma, and malignacy leading to spinal cord compression. Epidural abscesses of the spinal cord are of particular concern in IV drug abuser (even in the absence of fever).
Suspect what in an HIV-infected pt with altered mental status and a solitary, weakly ring-enhancing periventricular mass on MRI?
primary CNS lymphoma - EBV DNA in the CSF is specific for this condition.

Note: Toxoplasmosis is a good differential dx. However MRI should reveal MULTIPLE ring-enhancing lesions in the basal ganglia. Also, a positive Toxoplasma serology is quite common in normal subjects in the U.S. therefore not specific for toxoplasmosis!!!
Best diagnostic test in a pt suscpected to have acute glaucoma?
ocular tonometry
Common causes of acute delirium in the elderly?
UTI, pneumonia and metabolic disturbances. For this reason, always include urinalysis and measurement of serum electrolytes in the intial work-up.
DOC for initial therapy of absence seizures?
ETHOSUXIMIDE (used almost exclusively) and valproic acid - ethosuximide affects the thalamic neurons by working against calcium currents
Best initial symptomatic therapy for Parkinsonism?
elderly - L-dopa

younger pts - dopamine agonists

Note: does not stop progression of dz
When is selegiline used in Parkinsonism?
as an adjunctive treatment in pts receiving L-dopa - it is a selective MAO-B inhibitor that may slow progression of dz
When is amantadine used for Parkinsonism?
pts with mild disease who have NO disability - advantage of having low toxicity and improves all features of Parkinsonism.
When are anticholinergics used in Parkinsonism?
for pts whose predominant problem is resting tremor. Not encouraged in pts who are elderly, have dementia, or NO tremor.
What should be suspected when an older pt presents with FLUCTUATING cognitive impairment (pronounced variations in attention and alertness), recurrent and bizarre visual hallucinations, and motor features of Parkinsonism?
Lewy body dementia
Suspect what when an older pt presents with personality change (disinhibition, euphora, apathy), compulsive behaviors (peculiar eating habits, hyperorality), and impaired memory?
Pick's disease - a fronto-temporal dementia
Most likely location of the lesion in a pure motor stroke?
lacunar infarct of the posterior internal capsule (which carries corticospinal and corticobulbar motor fibers). Underlying pathology is thought to be a combination of microatheroma and lipohyalinosis and very rarely embolic in origin. Hypertension and DM are the most important risk factors. Comprise up to 25% of ischemic strokes and have much better prognosis than embolic strokes due to their small size. Often NOT appreciable on non-contrast CT scans.
Best way to confirm diagnosis of CLL?
flow cytometry to demonstrate lymphocyte clonality - CLL may present with lymphadenopathy but a significant number of pts are ASYMptomatic. Clues may be abnormally high WBC count on CBC with lymphocyte predominance. Peripheral smear may show atypical lymphocytes with "smudge" appearance.
What are diagnostic clues to G6PD deficiency?
bite cells and Heinz bodies (red blood cell inclusions) - G6PD is needed to create NADPH, which is in turn required to create glutathione and prevent the oxidation of hemoglobin into Heinz bodies. The denatured hemoglobin disrupts RBC membranes and causes hemolysis. This oxidation reaction typically occurs in response to drugs, fava beans, and infection.
PTT values will be _______ in the presence of lupus coagulant.
prolonged! this is strictly a laboratory artifact bc IgM/IgG immunoglobulin binds phopholipds used in the assay resulting in prolonged PTT. In actuality, these patients do not have bleeding problems BUT are HYPERcoagulable.
Suspect what in any pt with a hx of cancer that presents with acute back pain and neurological symptoms, particularly loss of bowel/bladder function?
Compression of the thecal sac aka epidural spinal cord compression due to a neoplastic cause - rapid recognition is necessary bc symptoms can rapidly progress to paralysis.

Other neruo symptoms aside from loss of bowel/bladder function may include imbalance, weakness, and weak rectal sphincter tone.

Confirm with MRI of the spine but do not delay initiation of glucorticoid treatment to reduce swelling and preserve neuro fxn while awaiting imaging results.
TTP-HUS should be suspected if what 4 characteristic features are present?
1) Hemolytic anemia
2) thrombocytopenia
3) renal failure
4) neuro symptoms (headache, confusion, etc)
Mechanism of TTP-HUS?
due to a deficiency of OR autoantibody against a specific von Willebrand factor-cleaving protease (ADAMTS-13). Causes accumulation of LARGE von Willebrand factor multimers and platelet aggregation. TTP-HUS is fatal in 80% if appropriate therapy is not promptly initiated so a high degree of clinical suspicion is necessary.

Tx of choice - plasmapheresis to remove the offending autoantibodies and replete the deficient enzyme.
Suspect what in a younger pt with anemia that is non-responsive to iron supplementation?
Thalassemia, especially if pt is of Mediterranean origin. Normally, there are two functional copies of the beta-hemoglobin gene but in thalassemia, there is a point mutation in one or both of these genes. This leads to reduced hemoglobin synthesis and eventually produces hypochromic microcytic anemia. Thalassemia comes in two severities:

beta-thalassemia minor - defect in 1 gene - modest anemia with MCV btn 55-75.

beta-thalassemia major - defect in both genes leading to severe anemia.
Age distribution for IBD?
bimodal - 20s-30s and 60s
what is transferrin saturation?
serum iron/TIBC

typically low in iron deficiency anemia but often normal in anemia of chronic dz.
most common causes of microcytic anemia?
iron deficiency, anemia of chronic disease, and thalassemia
Complications of multiple myeloma include?
renal failure, hypercalcemia, and hyperviscosity syndrome

Note: lytic bone lesions, marrow plasmacytosis, and urine/serum monoclonal proteins are classic findings!
Common causes of B12 deficiency:
total/partial gastrectomy, pernicious anemia, gastritis, disorders of the ileum preventing absorption, and old age.

Gastric DERIVED intrinsic factor must bind B12 for it to be absorbed by the ileum. B12 is necessary for purine synthesis.
Various manifestations of polycythemia vera?
increased RBC mass, mild granulocytosis, elevated platelet count, and LOW erythropoietin levels (ABSENCE of measurable URINE erythropoetin), INCR leukocyte alkaline phosphatase.

REVERSIBLE moderate hypertension 2dry to expanded blood volume.

BOTH bleeding and thrombosis can occur 2dry to elevated plt count and impaired plt function.
INCR incidence of peptic ulceration 2dry to histamine release from basophils).

INCR incidence of gouty arthritis 2dry to increased cell turnover.

PE may show plethoric face and splenomegaly. May complain of pruritus after bathing.

Phlebotomy to keep HCT < 45% is treatment of choice.
DOC for mild to moderate hypercalcemia due to malignancy?
bisphosphonates

Note: intravenous Zoledronic acid is recommended in ALL women with metastatic breast cancer and radiographic lytic bone dz and are receiving either hormone therapy or chemotherapy.
Mechanism of hypercalcemia of malignancy?
osteolytic metasases with local release of cytokines and tumor secretion of parathyroid hormone related peptide.
Suspect what in a pt with hundreds of ADENOMATOUS colonic polyps?
Familial colonic polyposis - 100% risk of cancer if not treated with a proctocolectomy!
difference btn HIT type 1 and type 2?
type 1 is fairly benign that resolves spontaneously whereas type 2 is caused by antibody formation to heparin-platelet 4 complex and can result in ARTERIAL thromboses.
Pts with pernicious anemia should be periodically screened for?
gastric cancer and castric carcinoid tumors bc increases risk by 2-3 times!

anit-intrinsic factor antibodies decrease the amount of functional intrinsic factor available to facilitate B12 absorption. Second, pts develop chronic atrophic gastritis due to the decreased prodxn of intrinsic factor by gastric parietal cells. Atrophic gastritis leads to incr risk of gastric cancer.
what is hyposthenuria?
nocturia 2dry to kidney's impaired ability to concentrate urine - found in pts with sickle cell disease or less sever in those with sickle cell trait. Red blood sickling in the vasa recta of the inner medulla impairs countercurrent exchange and free water reabsorption.
Suspect what in a pt with a chronic scar that develops into a non-healing, painLESS, bleeding ulcer?
Squamous cell carcinoma until proven otherwise - ulcers may become painFUL if ulcers do not heal. Tar derivatives (tobacco smoke) and other carcinogens and chronic radiation exposure are predisposing factors.

Dx is confirmed via punch biopsy!
typical age of pts with pernicious anemia?
most commonly occurs in the elderly but may affect younger pts as well, especially in the setting of other autoimmune conditions (e.g. vitiligo, autoimmune thyroid disease).

Note: dietary deficiency does NOT usually cause B12 deficiency as it does folate deficiency
Most common malignant bone tumor of youth?
osteosarcoma - classic radiologic findings of Codman's triangle and sunburst appearance. Average age at presentation is 15 years. Most commonly found in larger bones in the area of fastest bone growth rate (metaphyseal portions). Initial symptom is usually pain.

Tx is surgery
common cause of autoimmune platelet destruction?
Immune thrombocytopenic purpura - acute and self limited in children typically but insidious and chronic in adults.

tx is with systemic immunosuppression via steroids.
serum immunoelectrophoresis shows what in multiple myeloma?
characteristically an abnormal M-spike due to IgG antibody production by abnormal plasma cells.

this test is the best initial test when MM is suspected. BM biopsy can help confirm an abnormal result.
Management for pt with "soap bubble appearance" in the epiphyseal end of a long bone?
this is a giant cell tumor - refer to an orthopedic surgeon immediately
Firm, unilateral, NON-tender lymph nodes in an older pt with a smoking hx is suspicious for?
lymph node metastases where as similar findings in the HEAD/NECK are concerning for squamous cell carcinoma. Prompt biopsy is needed.
Turcot's syndrome?
brain tumors (primarily medulloblastomas and gliomas) PLUS colonic polyps (FAP or HNPCC).
Peutz-Jeghers syndrome?
intestinal hamartomatous polyps plus mucocutaneous melanocytic macules.
Multiple hamartoma syndrome (Cowden syndrome)?
GI-tract hamartomas plus Br CA, thyroid CA, and nodular gingival hyperplasia.
Medications that cause oxidative stress?
sulfa drugs (TMP-SMX), antimalarials, and nitrofurantoin
What are Heinz bodies?
When hemoglobin becomes oxidized to form methemoglobin, denatured globin, and sulfhemoglobin - conbines as insoluble masses (Heinz bodies) that attach to RBC membrane --> decr membrane pliability --> promotes RBC removal in spleen's reticuloendothelial system.
How can a leukemoid reaction (marked incr in leukocytes due to a severe infection/inflammation) be distinguished from CML?
they are INdistinguishable on peripheral blood smear. An INCR leukocyte alkaline phosphatase score is typical of a LEUKEMOID rxn.

Note: incr LAP score is also seen in polycythemia vera BUT these pts will have an ELEV RBC mass while ALL other cell lines are usually nml.
Erythropoietin levels and bone marrow response in anemia of chronic dz?
generally decreased and poor marrow response.
Step wise approach to breaking bad news to pts?
1) ensure quiet, private, and comfortable environment
2) "How much do you know about your symptoms?" to give an idea of the patient's expectations
3) "How much would you like to know about your condition?"
4) Give him a warning shot, "Unfortunately the situation is more serious than hoped."
5) Give results if pt wants to know....
6) Give prognosis and ALL options....
7) Be clear and simple as possible.
what should be considered in a pt that presents with ASYMptomatic thrombocytopenia but typical bone marrow and non-bone marrow causes have been ruled out?
initial presentation of HIV - in up to 10% of pts.
what is pagophagia?
pica (appetite for non-nutritive substances) for ice in particular.
What abnormalities in calcium, phosphate, potassium, and uric acid can be seen in tumor lysis syndrome?
both potassium and phosphate are intracellular ions so the breakdown of the cells releases excess amounts of these.

Released phosphage binds calcium --> hypocalcemia

degradation of cellular proteins ---> elevation of uric acid levels
Migratory thrombophlebitis (aka Trousseau's syndrome) along with symptoms of upper GI discomfort is suspicious for?
Pancreatic ADENOcarcinoma - abdominal CT should be initial diagonstic test of choice.
Lung cancer with the LEAST association to smoking?
Adenocarcinoma of the lung - usually peripherally located
Look for what cytochemical features when hairy cell leukemia is suspected?
tartrate-RESISTant acid phosphatase and CD11c marker.

It is a B-lymphocyte derived leukemia - bone marrow may become fibrotic leading to a dry tap.
Most common manifestation of hemophilia?
Hemarthroses withOUT significant trauma (even more common than spontaneous bruising). An x-linked disorder to a deficiency in either factor VIII (hemophilia A) or factor IX (hemophilia B).
Anticipated lab abnormalities and prophylactic treatment for loss of pregnancy in antiphospholipid antibody syndrome?
false positive VDRL, prolonged PTT, and thrombocytopenia.

Prophylaxis is with low dose aspirin and LMWH to avoid pregnancy loss
What can prevent a febrile transfusion reaction?
Leukocyte depletion techniques such as cell washing. Rxn is believed to be due to antibodies in the patient's plasma that react with the donor's leukocytes.
Tx for dermatitis herpetiformis (associated with celiac sprue)?
Dapsone
Areas commonly affected by seborrheic dermatitis?
eyebrows, nasolabial folds, bases of eyelashes, paranasal skin, and scalp (called cradle cap when scalp is involved).

It is a found in all age groups but relatively common in infancy. Transparent to yellow papules and scaling plaques are characteristic. Treatment is moisurizers, topical antifungals, anti-dandruff shampoo, and topical steroids.
Where is the latent infection of varicella zoster virus established?
sensory dorsal root ganglia
Rubella is caused by what organism?
RNA togavirus.

Tx with acetaminophen for symptomatic relief.
Why does recurrent chalazion (develops when a meibomian gland becomes obstructed) require histopathologic examination?
There is a risk for an underlying sebaceous (meibomian gland) carcinoma.

Note: This can be clinically difficult to distinguish fom basal cell carcinoma (most common malignancy of the lid margin).

**chalazion present as painful swellings of the lid margin that progresses to a nodular rubbery lesion.
What is a hordeolum?
A stye aka an acute infection of one of the glands of the eyelid. Usually due to Staph so treat with anti-staph abx and frequent hot compresses (to promote drainage).
Most commonly involved sites of warfarin-induced skin necrosis?
breasts, buttocks, thighs, and abdomen - initial complaint is pain, followed by bullae formation and skin necrosis. Occurs within weeks after starting therapy and is sometimes associated with Protein C deficiency.

Administer Vitamin K early, discontinue warfarin if lesion progresses, and use heparin to maintain anticoagulation until necrotic lesions heal.
What is pyoderma gangrenosum?
an ulcerative skin lesion - initially starts as a bite-like reaction iwth a small papule or pustule with pain as the main complaint.
A superficial skin lesion that is pruritic, erythematous, scaly, and has a red ring with a central clearing on a pre-adolescent is suspicious for?
Tinea corporis (ring worm) - typical in hot, humate weather. Dx with scraping and potassium hydroxide examination. treat with topical antifungals.
Molluscum contagiosum caused by poxvirus can be generalized if?
pt is immunodeficient such as AIDS, especially when CD4 is < 100/uL. Conjunctivitis may occur if the lid margins have been infected.
Sudden onset of pain and swelling at a site of trauma or recent surgery that progresses to purplish discoloration with gangrenous changes and signs of SYStemic toxicity is suspicious for?
Necrotizing fascitis - A gloved finger can easily be passed btn the 2 layers, revealing yellow green necrotic fascia which helps in the Dx. CT scan reveals necrosis, asymmetrical fascial thickening and gas!

Aggressively debride necrotic tissues and use high-flow oxygen, fluid resuscitation, plus broad-spectrum antibiotics to cover for aerobic and anaerobic organisms.
How does toxic epidermal necrolysis (TEN) manifest?
an erythematous morbilliform eruption that rapidly evolves into exfoliation of the skin (looks like the world's worst 3rd degree sunburn)! Patches of skin slide off with slight pressure (postitive Nikolsky's sign). Oral mucosa shows painful blisters which limits oral intake.

Often due to a drug reaction. Commonly involved drugs include sulfonamides, barbiturates, phenytoin, and NSAIDs.

Note: TEN is at the END of the spectrum for idiosyncratic skin rxns which includes Stevens Johnson syndrome and TEN/Stevens Johnson syndrome overlap. In Steven Johnson syndrome, up to 10% of the body surface area is involved whereas in TEN greater than 30% is involved. In between pts are labeled as TEN/Steven Johnson syndrome overlap.
What is seborrheic keratoses and is it worrisome?
Very common BENIGN growths that have a warty, stuck-on or cerebriform appearance. They are typically pigmented but may lack pigment and be pink/white to pale in color too.

Note: sometimes pruritic and tender!
Most common cause of acquired angioedema?
ACE-I - due to increased levels of pro-inflammatory action of bradykinin, which promotes edema, inflammation and pain. Typically presents within days to weeks after starting therapy but can occur at ANYTIME after starting meds.

Check for airway compromise and vasomotor instability, which requires epinephrine. Stop ACE-I therapy immediately.
What should be suspected in an infant boy that presents with fever, adenopathy, and numerous umbilicated vesicles over an area of healing atopic dermatitis?
Eczema herpeticum - a form of primary herpes simplex virus infection associated with atopic dermatitis. Infection in infants may be life-threatening, and acyclovir treatment should be initiated as soon as possible.
Common cutaneous associations of primary biliary cirrhosis?
xanthomas and xanthelasmas (soft, yellow plaques on medial aspect of the eyelids) due to reduced ability to absorb and store fat-soluble vitamins.
Diagnostic study of choice for a suspected melanoma?
Excisional biopsy - if the depth of the lesion is < 1 mm, excision with a 1 cm tumor free margin gives a 99% 5-year survival. Tumors greater than 1 mm in DEPTH should have a sentinel lymph node study.

Note: Excision with wide margins is not recommended until dx is confirmed. Incisional biopsy may miss the malignant focus within an otherwise normal nevus.
tx for mild acne (non-inflammatory comedonal acne)?
topical retinoids
tx for mild-to-moderate inflammatory acne?
topical retinoids plus topical abx
tx for papular and inflammatory acne (moderate-to-severe)?
oral abx
tx for nodulocystic and scarring acne?
oral isotretinoin
Best method of photo-protection from the sun?
Sun avoidance especially in the middle of the day (btn 10 AM and 4PM) remains the best method.

Inform pts that sunscreens should be applied 15-60 minutes PRIOR to sun exposure to allow enough time for protective film development.
What are strawberry hemangiomas (capillary hemangiomas) composed of?
thin walled blood vessels separated by connective tissue.
Suspect what in a pt that presents with diffusely blistered skin with flaccid bullae that appeared spontaneously, first starting in the mouth? Immunofluorescence shows IgG deposits INTRAcellularly in the EPIdermis.
Pemphigus vulgaris - the flaccid bullae are tender and painful when they rupture and have a positive Nikolsky's sign. It is due to autoantibodies against desmoglein.

Common tx is steroids. Immunosuppressives (azathioprine) may be used with prednisone and methotrexate.

Note: Bullous pemphigoid is a PRURitic dz with TENSE (not flaccid) blisters and oral lesions are RARE. Immunofluroescence shows IgG AND C3 in the dermal epidermal JUNCTION.
Pale, velvety pink or whitish, hypopigmented skin macules that do NOT tan and do not appear scaly, but scale on scraping is most likely due to?
tinea versicolor due to Malassezia furfur - skin scrapings after KOH will show large, blunt hyphae and thick-walled budding spores (classic spaghetti and meatballs appearance).

Tx topically with selenium sulfide lotion and ketaconazole shampoo. Change in pigmentation requires MONTHS to return to normal.
What causes toxic shock syndrome?
an EXOtoxin producing strain of S. aureus - exotoxin acts as a superantigen leading to massive cytokine release. Pts present with fevers, hypOtension, and generalized erythema that 1-2 weeks later can lead to desquamation of the palms and soles.
Stellate purpura with a central gunmetal gray color is a classic skin finding for?
acute meningococcemia - skin finding may affect up to 50% of affected pts and therefore can be KEY to a quick diagnosis.
Dry and rough skin with horny plates over the extensor surfaces of the limbs is a hallmark for ?
ichthyosis - condition worsens in the winter bc of incr dryness. can be hereditary or acquired.
What distinguishes a benzodiazepine overdose from an opioid overdose?
Benzodiazepine overdose lacks severe respiratory depression and lacks pupillary constriction.
What distinguishes alcohol and phenytoin inoxication from benzodiazepine overdose?
The presence of nystagmus in alcohol/phenytoin intoxication.
What should be first priority when there is any chemical contact with the eye?
immediate flushing of the affected eye with copius amounts of running water for at least 15 minutes. Obtaining medical care AFTERWARD is appropriate.

Note: With exposure of the eye to acid, there is a good chance of full recovery whereas with alkaline exposure, permanent corneal damage is more likely.
What should be first priority when there is a foreign body or cuts/scratches of the eye?
Obtaining medical care.
What is organophosphate poisoning?
Acetylcholinesterase is rendered non-functional leading to symptoms of cholinergic excess (bradycardia, miosis, bronchorrhea, muscle fasciculations, salivations, lacrimation, diarrhea, and urination).

Atropine should be given to compete with acetylcholine at muscarinic receptors to counteract the cholinergic excess. Immediate removal of the pt's clothing to prevent continuedaborption through the skin is also necessary.

Note:physostigmine (acetylcholinesterase inhibitor) would WORSEN this condition.
Best next step in mgmt for TCA overdose?
an emergent ECG to analyze the QRS complex.
What can confirm a suggested opioid intoxication?
Improvement of the pt's respiratory rate with NALOXONE administration (an opioid antagonist).
What drug is known to occasionally cause hypothermia by disrupting thermoregulation and the body's shivering mechanism?
fluphenazine - a high potency "typical" antipsychotic - pts should be advised to avoid prolonged exposure to extreme temperatures.
The most serious effect of alcohol withdrawal?
delirium tremens - occurs after 48-96 hours and consistsofhypertension, agitation, tachycardia,hallucinations, and fever. Mortality rate of up to 5%. Pt should be placedin aprotective environment and treated with benzodiazpeines - chlordiazepoxide is a common choice.
Hallucinations and withdrawal seizures from alcohol withdrawal can be seen when?
24-48 hours.
Early symptoms of reflex hyperactivity (anxiety, insomnia,tremors,and diaphoresis) in alcohol withdrawal can be seen when?
first 24 hours.
The most severe consequences of methanol intoxication are?
vision loss and coma - PE in methanol intoxication may reveal optic disc hyperemia while lab studies reveal ANION GAP metabolic acidosis. An increased OSMOLAR GAP is often seen as well.
Next best step in treatment for a pt who has ingested lye (sodium hydroxide)?
Upper GI endoscopy to evaluate the extent of damage. Damage from alkaline solutions cause almost instantaneous liquefactive necrosis of the esophageal wall which can lead to perforation and mediastinitis. Efforts to neutralize the alkali, induce vomiting, or administer charcoal does not improve outcomes and in fact complicates management. Gastric decontamination with ipecac to induce vomiting will only RE-expose the esophagus to lye causing more injury. Activated charcoal will obstruct the view during endoscopy. And, neutralization will not reverse the INSTANTaneous damage caused by lye and will make things worse by generating heat.
When is administration of activated charcoal helpful?
Within one hour of non-alkaline poison.
Most common associated electrolye abnormality in Addison's (primary adrenal failure) disease?
hypOnatremia. hyperkalemia is also common.
Signs of septic shock?
acidosis(due to accumulation of lactate 2dry to tissue hypoxia and anaerobic respiration resulting from hypotension related to septic shock), low urine output, hypOtension, tachypnea, fever.
What does sodium plystyrene sulfonate (kayexalate) do?
A potassium-binding resin that decr total body potassium through the gut. Sodium is exchanged for potassium. It takes at least 1-2 hours to work.

Insulin and glucose is much more rapid-acting taking only 15-30 minutes to drive potassium intracellularly.
How to tell if metabolic alkalosis is "chloride-sensitive?"
LOW URINary chloride excretion (<20 mEq/day) and saline-RESPONSIVE volume depletion.
How to tell if metabolic alkalosis is "chloride resistant?"
normal serum chlorine --> normal urine chloride

saline UNresponsive
Electrolyte abnormality in Cushing's syndrome?
hypOkalemia and hypERnatremia - excessive cortisol which also means excess mineralocorticoid activity causing renal potassium wasting. Severe Cushing's can be treated with an aldosterone antagonist like spironolactone.
Most common organisms involved in subacute (already present valvular abnormality) bacterial endocarditis?
1) Viridans group (usually from upper respiratory)
2) enterococci - usually if genitourinary infections or GU procedures (ie.cystoscopy) have taken place
3) coagulase-negative staph (such as S. epidermidis) - usually from skin

Note: S. aureus is common in acute, severe illness with NORMAL heart valves
Potential side effects of amiodorone (an antiarrhythmic):
1) thyroid dysfunction
2) pulmonary fibrosis
3) hepatotoxicity
Diagnostic criteria for ARDS:
1) acute onset
2) PaO2/FIO2 < 200
3) the presence of bilateral infiltrates on CXR
4) Swan Ganz pressure (measures PCWP) <18

Note: LOW PCWP and absence of JVD aids in distinguishing ARDS from CHF. ARDS is a form of NON-cardiogenic pulmonary edema
First step in management of SYMPTOMATIC sinus bradycardia?
treat with IV atropine bc it decreases vagal input

Note: use epinephrine in hemodynamically UNstable patients with sinus brady.
Causes of sinus brady:
excellent physical conditioning, exaggerated vagal activity, sick sinus syndrome, hypOglycemia and certain meds (digitalis, b-blockers, Ca Ch blockers).
How does prolonged, tachysystolic atrial fibrillation effect the left ventricle?
causes LV DILATION and a DEPRESSED ejection fraction.
Most important priority when managing prolonged, tachysystolic atrial fibrillation?
controlling the rhythm or rate - improves LV function significantly and sometimes dramatically
Classic symptoms that indicate need for surgery in patients with aortic stenosis?
ASD
angina
syncope
dyspnea

onset of any of these 3 symptoms (especially dyspnea) indicates poor prognosis withOUT surgery (50% 3-year mortality rate).
Indications for aortic valve replacement (3):
1) ALL SYMptomatic patients with AS
2) patients with severe AS already undergoing CABG or other valvular surgery
3) ASYMptomatic patients with severe AS and EITHER poor LV systolic function, LVH > 15 mm, valve area < 0.6 cm2, OR abnormal response to exercise
Definition of PEA pulseless electrical activity?
DISCERNIBLE rhythm on cardiac monitoring BUT clinical cardiac arrest, i.e. NO palpable pulses or BP

Best management: manual chest compressions and CPR

Note: UNLIKE VF/VT, this is NOT a shockable rhythm
When is synchronized electrical cardioversion used?
To convert a patient with a PERFUSING tachyarrhythmia (i.e. positive pulses and BP) BUT with SERIOUS hemodynamic compromise nonetheless.
Management for a pt showing evidence of a STEMI plus flash pulmonary edema (acute heart failure causing pulmonary edema)?
Furosemide - diuresis to reduce preload thereby decreasing pulmonary capillary pressure. Also causes VENOdilation, also decreasing preload.

Morphine is also beneficial for both anxiolytic AND PRELOAD reducing effects.

Nitrates, oxygen, and heparin should be given as in all MI's.

B-blockers, although standard therapy in MI, should be AVOIDED as it can worsen acute heart failure.
Chronic hypoxemia in COPD causes?
constriction of the pulmonary ARTERIAL system leading to pulmonary HTN --> RVH --> right heart failure

Note: pulmonary CAPILLARY wedge pressure reflects the LEFT ATRIAL pressure
Blood pressure control and salt restriction can help alleviate edema 2dry to:
LEFT heart failure - a clue may be crackles on lung auscultation
Smoking cessation and oxygen therapy will improve edema 2dry to:
RIGHT heart failure from increased pulmonary ARTERY pressure

Clues may be evidence of cor pulmonale such as elevated JVP or ascites
Best intervention to reduce AAA PROGRESSION when surgery is not indicated?
smoking cessation!

antihypertensives, reducing cholesterol, improving DM, and alcohol cessation are all good but not as effective in reducing AAA progression.
Common causes of amyloidosis?
Chronic inflammatory disease such as rheumatoid arthritis and multiple myeloma.

Can result in involvement of heart, liver and kidney.
How does amyloidosis involve the heart, liver, and kidney?
deposition of amyloid fibrils:
in kidney - results in proteinuria
in heart - results in RESTRICTIVE cardiomyopathy with thick ventricular walls and diastolic dysfunction BUT PRESERVED ventricular dimensions--> CHF

liver - inhibits the synthesis of coagulation factors resultin in increased bruisability
Electrical alternans (amplitude of the QRS alternates) signifies?
cardiac tamponade

Remember that an URI can lead to pericarditis causing a pericardial EFFUSION and resulting in tamponade. Decreased preload and CO can lead to syncope from decreased cranial blood flow.

Treatment is massive volume resusciation and emergent pericardiocentesis.
Isolated systolic HTN (as indicated by widened pulse pressure) is an important cause of HTN in ELDERLY patients is caused by?
decreased ELASTIC properties of the arterial wall - ALWAYS treat despite fact that diastolic pressure is not elevated. Hydrochlorthiazide is DOC.
The cause of generalized edema in patients with end stage renal disease as well as glomerulonephritis?
decreased GFR (can present with TRACE proteinuria)
Outflow obstruction in hypertrophic cardiomyopathy results from?
both septal hypertrophy AND systolic anterior motion (SAM) of the mitral valve
The most common cause of Afib is?
HTN causing DIASTOLIC dysfunction (aka heart failure with preserved left venricular ejection fraction). Diastolic dysfunction refers to impaired filling of the left or right ventricle EITHER bc of impaired myocardial relaxation or a stiff, non compliant ventricle. Contractility may remain normal (i.e. normal EF) but increased diastolic pressures reduces cardiac output.

Chronically elevated LV DIASTOLIC pressures cause left atrial pressures to rise which in turn can lead to Afib.

Treatment is with antihypertensives and DIURETICS when decompensated heart failure signs begin.
What occurs in more than 30% of cases of INFERIOR wall MI?

Best management?
Right ventricular infarction - clues may be clear lung fields (although if LV infarction is severe enough to cause pulmonary edema, this may not be the case), JVD, and hypOtension.

IV fluid resuscitation to increase RV stroke volume and enhance left ventricular filling. Avoid any medication that reduces preload (NITRATES or diuretics) bc this will exacerbate symptoms.
In what settings are nitrates NOT indicated?
aortic stenosis

recent phosphodiesterase inhibitor use

R ventricular infarction (30% of cases with inferior wall MIs)
3 causes of pulsus paradoxus (difference in SBP of > 12 mm Hg during inspiration)?
1) cardiac tamponade
2) tension pneumothorax
3) severe asthma
Why does systolic pressure drop during inspiration? Why does it drop more in scenarios that cause pulsus paradoxus such as tamponade, tension pneumothorax and severe asthma?
increased venous return to the right heart causes impaired LVH filling due to COMPRESSION of the left ventricle.

elevated intraTHORACIC pressures during inhalation are thought to FURTHER exacerbate compression of the left ventricle.
Common side effect of dihydropyridine Ca-Ch antagonists such as amlodipine?
peripheral edema due to dilation of peripheral vessels
Drugs other than ACE-inhibitors that have shown to have a mortality benefit in CHF?
B-blockers, angiotensin II receptor blockers, and spironolactone.
Initial investigation of choice in suspected aortic dissection?
TEE but ONLY AFTER hypertension treatment is initiated.
leading cause of constrictive pericarditis WORLDwide?
TB
Most common cause of 2dry hypertension, especially in those with RESISTANT htn and evidence of atherosclerotic disease?
renal artery stenosis

clue may be a systolic and diastolic periumbilical murmur with the diastolic component more specific for renal artery stenosis.
Subclavian artery atherosclerosis has a preference for _____ artery?
the left artery - manifests as higher blood pressure in left arm versus the right arm

note: higher blood pressure in the right arm or arms pressure > leg pressure is more indicative of coarctation of the aorta.
Increased risk for maternal cervical insufficiency?
past GYN procedures (LEEP, cone biopsy), DES exposure, multiple gestation, preterm birth, or second trimester pregnancy loss.
gold standard for evaluating the cervix for cervical incompetence?
TRANSvaginal ultrasound - cervical length should be > 25 mm at 24 weeks gestation
what is more sensitive to outliers - the mean, median or mode?
the mean is very sensitive to outliers and easily shifts toward them
Limiting side effects of nicotinic acid for increasing HDL?
flushing (80%), pruritus (2-%), nausea, or paresthesias - limited by using a controlled-release form of the medication
What is a common hip disorder seen in overweight adolescents?
slipped capital femoral epiphysis - children with endocrine issues are more likely to have bilat dz and to present at an earlier age. On examination, pts hold the hip in passive external rotation and exhibit decreased internal rotation, abduction and flexion.

DX is made via plain XR of the hip (AP and frog leg lateral views). Tx is surgical fixation at the current degree of slippage to avoid risk of avascular necrosis.
Why do Turner's patients have a higher risk of osteoperosis?
lower estrogen levels and bc they have only one copy of the X chromosome genes involved in bone metabolism.
best means of evaluating liver damage in patients with acute hepatitis vs. chronic hepatitis (hepatitis >6 months)?
acute - LFTs and viral serology

chronic - liver biopsy
gastric outlet obstruction is characterized by what symptoms? Major causes of gastric outlet obstruction?
early satiety, nausea, non-bilous vomiting, and weight loss (diabetic gastroparesis presents in a similar way)

causes: PUD, strictures 2dry to ingestion of caustic agents, pyloric stenosis, and pancreatic cancer
Most commonly injured rotator cuff muscle?
SUPRAspinatus
What is the drop arm sign?
Arm is abducted passively to greater than 90 degrees and asked to lower arm slowly. With complete rotator cuff tear, the pt will be unable to lower the arm smoothly and will appear to drop rapidly from near the 90 degree position.
What will a biopsy show in laxative abuse?
dark brown discoloration of the colon with lymph follicles shining through as pale patches (melanosis coli).
A deadly complication of cirrhosis characterized by renal failure that does not respond to volume resuscitation?
hepatorenal syndrome - best treated with liver transplantation. ACE-I and low-dose dopamine proves to be of no benefit
The typical cause of erectile dysfunction from a pelvic fracture and urethral injury?
NERVE injury and altered ARTERIAL supply - not veins
The typical cause of erectile dysfunction from a penile injury?
venogenic
Endocrinologic causes of erectile dysfunction?
hyperprolactinemia, testosterone deficiency, and DM
5 phases of iron intoxication:
1) GI phase with direct mucosal damage (30 min - 6 hours) - N/V, hematemesis (coffee ground emesis), melena, abdominal pain
2) latent phase (6-24 hours) - mostly asymptomatic
3) Shock and metabolic acidosis (12-96 hours)
4) hepatotoxicity (12-96 hours)
5) Bowel obstruction 2dry to mucosal scarring - several weeks post-ingestion
Main substrates of gluconeogenesis?
alanine, lactate, and glycerol-3-phosphate

pyruvate is an intermediate during gluconeogenesis
Give tetanus-diptheria TOXOID in what scenarios?
in almost all scenarios EXCEPT if pt received the booster <10 years and the wound is MINOR and clean

Note: in more severe or dirty wounds with unknown immune status or booster given >10 years, give toxoid AND tetanus immune globulin
3 major treatment options of Grave's dz?
1) Radioactive iodine ablation: preferred in the US
2) antithyroid drug therapy - propylthiouracil OR methimazole
3) thyroidectomy

Serious side effect of antithyroid drug: agranulocytosis. Pts advised to stop if sore throat and fever arise and the WBC count is checked. Routine monitoring is NOT helpful.
True or false: A pregnant woman has the right to refuse treatment, even if it places her unborn child at risk.
True
Suspect what in an HIV pt with pleuritic pain and CAVITATING lung nodules on CXR?
tricuspid endocarditis caused by S. aureus from IV drug use - fragments of vegetation from the tricuspid valve can embolize to the lungs as nodules that cavitate
top three risk factors for NASH?
obesity, DM, hypertricglyceridemia

other risk factors include TPN, endocrinopathies, and use of certain meds (corticosteroids, amodorone, diltiazem, tamoxifen, HAART).
Most common cause of 2dry HTN in children?
Fibromuscular dysplasia - can present as new onset HTN in children. Bruit or venous hum can be heard at costovertebral angle. Angiogram reveals the "string of beads" sign.
Recommended chemoprophylaxis for people traveling to Sub-saharan Africa or the Indian subcontinent?
Mefloquine for chloroquine-resistant Plasmodium falciparum - start one week before travel and continue 4 weeks after departure from endemic area
What is caused by autoimmune destruction of melanocytes and peaks in persons aged 20-30 years?
vitiligo - macular depigmentation that involves the peri-orificial and acral areas
An anticonvulsant agent which can be used to treat benign essential tremors but may precipitate acute intermittent porphyria which manifests as abdominal pain, neurologic and psychiatric abnormalities?
Primidone - check for urine porphobilinogen if this side effect is suspected
Chronic hepatitis C is associated with a number of EXTRA-hepatic complications like:
1) cryoglobulinemia
2) Bcell lymphomas
3) Plasmacytomas
4) Autoimmune dz like Sjogren's syndrome and thyroiditis
5) Lichen planus
6) Porphyria cutanea tarda
7) Idiopathic thrombocytopenic purpura
8) membranoproliferative glomerlunephritis (2dry to cryoglobulinemia)
Three complications that can lead to hypOtension btn day 3-7 after an MI:
1) Mitral regurg due to papillary muscle rupture - pansystolic murmur loudest at the apex with radiation to the axila (classic of MR)

2) Left ventricle free wall rupture - JVD, distant heart sounds, pericardial rub, and pulsus paradoxus (all 2dry to tamponade)

3) Interventricular septum rupture - pansystolic murmur heard best at left sternal border.
Why does CF often present as failure to thrive?
Due to fat and protein malabsorption from pancreatic insufficiency.

Pts may also have dry skin (Vit A deficiency), epistaxis (Vit K deficiency), meconium ileus at birth, and infertility.
Suspect what in any patient with a hx of tick bite, systemic symptoms, leukopenia, and/or thrombocytopenia, and elev aminotransferases?
Ehrlichiosis - incubation period varies from 1-3 weeks. Also known as the spotLESS Rocky Mountain fever bc there is usually NO rash. Peripheral blood smear may show intracellular WBC inclusions called morulae but such diagnosis is NOT necessary for starting treatment.

DOC=doxycyline (same as for Lyme dz and RMSF).
Treatment for pregnant women with RMSF?
Chloramphenicol
What acid-base status is seen in COPD patients?
respiratory acidosis due to chronic CO2 retention.
Treatment that is often used in COPD patients who have developed signs of cor pulmonale (elev JVP, hepatomegaly, and peripheral edema, all present with CLEAR lungs) but must be used cautiously so that cardiac output is not reduced to the point of subsequent renal failure?
loop diuretics - may also see hypOkalemia as result.
depressed cardiac output plus an elevated PCWP is indicative of?
left ventricular failure. As a result, systemic vascular resistance is increased (mediated by sympathetic neurohumoral activation, renin-angiotensin system activation) in attempt to preserve cardiac output and maintain tissue perfusion.

Remember: PCWP is an indicator of left ATRIAL pressure, and most of the times left ventricular END-DIASTOLIC pressure too).
What does an anion gap represent?
concentration of UNmeasured serum ANIONS - it is increased by the abnormal presence of NON-CHLORINATED acids in the serum such as MUDPILES.
The two most common explanations for inflammatory monoarthrits?
septic arthritis and crystal-induced arthritis: given the potential for joint destruction from septic arthritis, it should be considered the cause of inflammatory monoarthritis until proven otherwise.

Synovial fluid analysis, gram stain and culture are critical for distinguishing septic from crystal-induced arthritis.
Patients with rheumatoid arthritishave an increased risk of what other type of arthritis?
septic arthritis from S. aureus.
Most common indication for hysterectomy?
uterine fibroids
uterine fibroids grow in response to what hormone?
estrogen - so become larger with OCPs and during pregnancy; often regress after menopause
Features of an innocent murmur in children?
asymptomatic
systolic ejection quality
less than grade 2 of 4 intensity
VARIES with position
normal S2 sound
no other extra sounds
normal pulses
What is sample distortion bias?
when the study sample is not representative of the target population with respect to distribution of exposure and outcome
What is information bias?
imperfect assessment of association between exposure and outcome as a result of errors in measurement. Can be minimized by using standardized techniques as well as trained observers.
What is confounding bias?
presence of one or more variables associated INDEPENDENTLY with both exposure and outcome.
Recurrent pneumonia in the same anatomic location is a red flag for?
lung cancer, especially in a smoker. Initial investigation of choice is a CT scan of the chest to look for a mass. A bronchoscopy guided biopsy should be done for PERIbronchial mass, whereas a CT-guided biopsy should be used for a PERIPHERAL mass.
True or false? A physician is authorized to provide emergent life-saving treatment to an unconscious patient who does not have a living will despite a spouse requesting treatment be witheld for religious reasons?
true
How does an infant with C. botulinum in the intestinal tract present?
often with CONSTIPATION and poor feeding. This is followed by progressive hypotonia, weakness, loss of DTRs, cranial nerve abnormalities (impaired gag reflex, ptosis, mydriasis), and respiratory difficulties. Signs of autonomic dysfunction such as hypotension and neurogenic bladder can occur early too.

Note: Do not confuse with C. botulinum TOXIN intake which causes pseudomembranous colitis with diarrhea. This is ingestion of food with actual C. botulinum organism which grows in the gut and produces toxin responsible for blocking acetylcholine release.
Management of a septic abortion?
1) cervical and blood culture
2) antibiotics
3) GENTLE suction curettage to remove infectious nidus

Note: vigorous suction curettage may cause perforation of the uterus and should be avoided.
The most common cause of death in patients with an MI?
Vfib-a RENTRANT arrhythmia
Patients with an epidural hematoma may present with what focal neuro signs?
ipsilateral dilation of the pupil (caused by oculomotor nerve compression) along with ipsilateral hemiparesis.
Borrelia burgdorferi causes?
Lyme disease - intermittent inflammatory arthritis is a typical PRESENTation
Reliability or reproducibility is a measure of?
random error
INternal validity is the same thing as?
bias
External validity or generalizability means?
the extent to which results of a study are applicable to other populations. For example, a study conducted in middle-aged women would not be applicable to elderly men.
How to distinguish gonococcal vs. chlamydial conjunctivitis in an infant?
gonococcal - btn 2-5 days and very purulent

chlamydial - greater than 5 days and LESS purulent

Note: chemical conjunctivitis from prophylactic drops occurs in the 1st 24 hours and is mild
Priorities in managing a rib fracture?
analgesia to allow proper ventilation and prevent atelecatasis/pneumonia. NSAIDs and opiates are commonly used but an intercostal nerve block can also be used if oral meds are not sufficient.

Note: opiates may depress respiratory function but a nerve block carries some risk of pneumothorax
What is an inflammatory change in the medial CANTHAL region of the eye usually due to S. aureus or beta-hemolytic Streptococcus?
Dacrocystitis
What is bronchoalveolar lavage and when is it useful?
A method of sampling lung cells during bronchoscopy - it has the greatest diagnostic utility in the evaluation of suspected malignancy or an opportunistic infection.

Note: It has a well-established role in dx of PCP AFTER sputum induction (which is less invasive) does not yield a diagnosis.
Age for colonoscopy screening?
50 for average risk patients.

For patients with an affected first-degree relative, screening should begin 10 years before the age the relative was DIAGNOSED.
If dantrolene is not available for the treatment of neuroleptic malignant syndrome, what can be used as an alternative?
bromocriptine (a dopamine agonist) and amantadine (an antiviral drug with dopaminergic properties).
How to distinguish the vascular claudication of PVD from the "neurogenic claudication" of spinal stenosis?
PVD-induced claudication is EXERTION dependent and resolves while standing STILL. Neurogenic claudication is POSITION-dependent and resolves with sitting or laying but PERSISTS while standing still.
Dementia that has a fluctuating cognitive impairment and often bizarre, visual hallucinations?
Lewy body dementia
What can cause painLESS blisters, increased fragility on the dorsal hand surface, facial hypertrichosis, and hyperpigmentation that is often associated with Hepatitis C infection?
Porphyria cutanea tarda - from a deficiency of uroporphyrinogen decarboxylase (an enzyme in the heme synthesis pathway). It can be triggered by ingestion of certain substances like ethanol or estrogens and should be discontinued.
Tx for porphyria cutanea tarda?
phlebotomy or hydroxychoroquine may provide reliev

interferon-alpha if pt is simultaneously infected with Hep C.
What is Ramsay Hunt syndrome?
a form of herpes zoster that causes Bell's palsy - vesicles are seen on the outer ear.
When should a pt with asthma be prescribed an inhaled LOW-dose corticosteroid (in addition to the preexisting PRN albuterol inhaler)?
When symptoms are > 2 days/wk with nighttime awakenings 3-4x/month, minor limitation of activities, and normal FEV1.
when should an asthma pt on PRN albuterol inhaler and corticosteroid inhaler be prescribed a long-acting beta-2 inhaler?
Daily asthma symptoms, frequent nighttime awakenings, extremely limited activity, and FEV1<60% predicted. Corticosteroid inhaler should also be upgraded to a HIGH-dose.
How should palpation of the vertex at the fundus before 37 weeks gestation be managed?
Routine follow up as most will self-correct by week 37. External cephalic version is inicated if breech presentation persists after 37 weeks.
When is serologic testing with ELISA, followed by western blot for Lyme disease performed?
in patients with intermediate pretest possibility such as those with no clear hx of tick bite but probable exposure and positive s/sx.
Dissection of aorta can extend into the pericardium, coronary arteries or carotid arteries, leading to...?
cardiac tamponade, MI, or stroke, respectively.
positive McMurray sign is specific for?
meniscal injury
Standard management of solitary lesion brain metastasis?
surgical resection followed by whole brain radiation.
Standard management of MULTIPLE brain metastases?
palliative whole brain radiation
What should be suspected in a pt with GI symptoms including abdominal pain, diarrhea, and malabsorption with distention, flatulence and steatorrhea PLUS fever, weight loss, arthralgias, skin hyperpigmentation, chronic cough, and heart murmur?
Whipple's dz - a MULTI-system illness caused by bacillus Tropheryma whippelii - most common in white men during the 4th-6th decades.

EXTRA-intestinal manifestions include migratory polyarthropathy, chronic cough, and myocardial/valvular involvement leading to CHF or regurg. Later stages of dz may include dementia and other CNS findings such as supranuclear ophthalmoplegia and myoclonus.

Biopsy will show PAS-positive material in lamina propria of the small intestine.
When is D-xylose absorption abnormal?
Both in bacterial overgrowth and celiac dz. However, with bacterial overgrowth, absorption becomes normal after antibiotic treatment.

Note: Absorption of D-xylose ONLY requires INTACT mucosa in the PROXIMAL small bowel so is unaffected by the other fat malabsorptive diseases such as pancreatic insufficiency and Crohn's.
When should screening for colon cancer begin in a pt with ulcerative colitis?
8 years after diagnosis with repeat colonoscopy once every 1-2 years.
What should be suspected in a fairly young AA pt who presents with progressive dyspnea and dry cough PLUS erythema nodosum and a hx of uveitis?
Sarcoidosis - 25% will develop anterior uveitis which is usually self-limited but can sometimes progress to blindness.

CXR shows bilateral hilar lymphadenopathy and/or diffiuse interstitial infiltrates.
What does VIPoma=pancreatic cholera mean?
a rare pancreatic cancerous tumor that causes severe watery diarrhea PLUS hypokalemia (may manifest as leg cramps). Other symptoms include dehydration, abdominal pain/cramping, weight loss, facial flushing and redness.

Tx: First correct dehydration. Second slow diarrhea with meds like ocreotide. Third, surgically remove if no metastasis will often cure dz.
What is tamoxifen's effects on breast tissue, endometrium, and bone?
antagonist to breast tissue DECR CA

agonist to endometrium INCR CA

agonist to bone osteoclasts DECR osteoperosis
What pregnant women should be screened for syphillis?
ALL of them regardless of risk factors (at first prenatal visit)
What pregnant women should be screened for chlamydia?
Under the age of 24 or at high-risk (hx of STDs, new/multiple partners)
Frequent comorbid conditions in Tourette syndrome?
ADHD (60%) or obsessive-compulsive disorder (27%).
Treatment of choice in schizophrenia patient that is noncompliant with medication?
Depot antipsychotics such as fluphenazine and haloperidol.
Treatment for hepatic encephalopathy?
1) Treat underlying precipitant
2) Lactulose - a nonabsorbable disaccharide syrup that is converted into ACIDS by colonic bacteria. This acidification causes catharsis and a decrease in circulating ammonia levels.
3) Antibiotics may help in decreasing the number of ammonia-producing bacteria
4) Laxatives also promote catharsis and may be of some benefit.
When should children develop separation anxiety?
Btn 9-18 months
What may be the only indication of a diaphragmatic hernia in a patient with blunt abdominal trauma?
An elevated LEFT diaphragm on CXR. Patients usually have respiratory distress and deviation of mediastinal contents to the opposite side.

Early diagnosis is important bc therre is a high rate of mortality and bowel strangulation may be up to 30%.
Antidote for TCA or aspirin overdose?
sodium bicarbonate
Tx for torsades de points?
Magnesium sulfate
Tx for severe lithium toxicity?
hemodialysis
antidote for moderate to severe lead poisoning?
Calcium EDTA

oral succimer can be used in mild to mod lead poisoning.
What is cardioprotective in cases of hyperkalemia?
Calcium gluconate
antidote for acetaminophen?
N-acetylcysteine
Management of pt who presents with lab findings indicative for lupus nephritis?
renal biopsy to determine the class of nephritis. Different types of nephritis require different therapies.
Why may a patient with BPH present with an inability to void when in severe pain?
inability to Valsava due to pain
Most frequent cause of NON-traumatic subarachnoid hemorrhage?
rupture of saccular aneurysm, especially when larger than 7 mm or present in the anterior circulation of the circle of Willis.
Side effects of niacin can be reduced with what drug?
low dose aspirin to negate the prostaglandin-induced peripheral vasodilation
Smudge cells are characteristically seen in what type of leukemia?
CLL
Reid Sternberg cells are pathognomonic for?
Hodgkin's dz
nasopharyngeal carcinoma is strongly associated with?
EBV infection - common in pts of Mediterranean and Far Eastern descent

Often presents with recurrent otitis media, recurrent epistaxis, or nasal obstruction
Management of an arterial embolus?
1) heparin therapy immediately without delay for confirmatory testing
2) percutaneous thrombolysis (i.e. intra-arterial fibrinolysis AT SITE of embolus)/mechanical embolectomy or surgical embolectomy.
What is a malabsorption syndrome which can be associated with a hx of abdominal surgery?
bacterial overgrowth - pts in severe and advanced cases may present with tetany (hypocalcemia due to Vit D deficiency), night blindness due to Vit A deficiency, neuropathy due to vit B-12 deficiency, dermatitis, arthritis, and hepatic injury.
Comorbidities associated with vitiligo?
autoimmune conditions such as pernicious anemia, DMT1, primary adrenal insufficiency, hypopituitarism, autoimmune thyroid dz, and alopecia areata.
autosomal dominant polycystic kidney dz may involve enlargement of which organ(s)?
bilateral kidneys (note that the right one is often palpable since it lies lower than the left one)

liver due to cystic involvement
first step in tx of pseudotumor cerebri?
acetazolamide bc it inhibits choroid plexus carboinc anhydrase and thus reduces CSF.

Note: Do not do a lumbar puncture unless you have radiographic conformation that there is NO space occupying lesion causing increased intracranial pressure.

Also note that the goal of treatment is to prevent visual loss and to reduce intracranial pressure for symptomatic relief.
What is suspected in a pt that presents with non-purulent vesicles on the fingers or hand and multinucleated giant cells on the Tzanck smear of the vesicles?
Herpetic whitlow - caused by either type 1 or type 2 herpes simplex virus and is SELF-limiting. Health care workers who come in contact with infected orotracheal secretions are at increased risk of developing whitlow.
formula for calculating serum osmolality?
2(serum Na) + blood glucose/18 + BUN/2.8
what characterizes hyperglycemic, hyper osmolar non-ketotic coma?
EXTREMELY high blood glucose, plasma hyperosmolality, NORMAL anion gap, and NEG serum ketones
Treatment for hepatitis A?
a self-limiting condition so mainly supportive with complete recovery in 3-6 weeks.

Close contacts of individuals with Hep A should be given immune globulin.
What lab abnormalities are common in sarcoidosis?
Elevated Ca and ACE levels
Tx of choice in sarcoidosis
steroids
Pathophysiology seen on biopsy of sarcoidosis?
non-caseating GRANULOMAS
Suspect what in a pt that presents with slowly progressive proximal muslce weakness of the lower extremities characterized by difficulty with stair climbing or rising from a seated position? Muscle tenderness may be present. No SKIN findings and the muscles of mastication and facial expression are spared.
Polymyositis - an inflammatory muscle dz of unknown etiology. Muscle biopsy is diagnostic study of choice.
Most sensitive and specific tests for diagnosis of acute pancreatitis?
serum lipase > serum amylase

Patients who FAIL to IMPROVE with conservative treatment of acute pancreatitis, should undergo an abdominal CT to search for areas of infection and necrosis.
3 key principles to the use of pain meds in patients with terminal stages of cancer?
1) use non-narcotics first unless you are SURE that the patient is in severe pain from your clinical judgement
2) Do not be afraid to give narcotics
3) Prescribe adequate amounts - START with SHORT ACTING morphine and titrate doses until adequate pain control is established.

Then switch to LONG-acting narcotics and use short-acting morphine for break through pain.
Discovery of iron-deficiency anemia in an adult male or a post-menopausal woman should prompt investigation for?
occult GI blood loss, often due to a right sided colon cancer. Other GI causes may be PUD, angiodysplasia, colonic diverticula.

Note: testing for occult blood should be done even if iron studies indicate depressed serum iron and ferritin levels.
ototoxic medications?
loop diuretics!
aminoglycosides!
also aspirin and chemotherapeutic agents.

Note: higer doses of furosemide, coexistant renal failure, or other concurrent ototoxic meds increase the risk of this side effect.
Suspect ________ in a pneumonia with prominent GI symptoms such as diarrhea, hypOnatremia, and LFT abnormalities?
Legionella - diagnose with urinary antigen. Tx with quinolone or a macrolide.
Suspect what when a 40-year school teacher presents with acute onset polyarticular and symmetric arthritis of teh MCP, PIP, wrist, and ankle joints but NO fever, weight loss or rash.
Parvovirus - amongst the most common causes of viral arthritis especially in those in close contact with children. "Slapped cheek" appearance is often absent in adults and the most common finding is arthritis.

Self limiting - resolves within 2 months. Confirm with detection of ANTI-B19 IgM ANTIBODIES.
What happens to the following in a restrictive lung disease such as idiopathic pulmonary fibrosis...
A-a gradient
diffusing capacity
V/Q
TLC
residual volume
FEV1/FVC
A-a gradient=INCR
diffusing capacity=reduced
V/Q=mismatched, reduced
TLC=reduced
residual volume=reduced
FEV1/FVC=normal to increased
What does PEEP do?
Maintains airway pressure above atmospheric pressure at the end of EXPiration.
Known complications of ventilation with a high PEEP?
alveolar damage, pneumothorax, and hypotension, especially pts with fragile lung parenchyma such as those with ARDS.

Can result in tension pneumothorax --> compression of mediastinum and impaired ventricular filling --> hypotension, tachycardia, tracheal deviation, and unilateral absence of breath sounds.
Suspect what in a patient presenting with s/sx of systolic heart failure plus thrombocytopenia, macrocytosis, and elevated transaminases suggestive of alcoholism?
dilated cardiomyopathy 2dry to alcoholism. Measure most likely to REVERSE heart failure is abstinence from alcohol.

Note: ACE-I should be given and will slow the progression of heart failure but will NOT reverse the dz process.
What is the major source of estrogen in menopausal women?
peripheral conversion of ADRENAL androgens by the aromatase enzyme present in ADIPOSE tissue.
What is a medication that is helpful in a pt with depression as well as difficulty with smoking cessation?
Bupropion
Disorder characterized by emotional/behavioral symptoms that develop wi 3 months of exposure to an identifiable stressor and rarely last more than 6 months after the stressor has ended?
Adjustment disorder - marked distress in EXCESS of what is expected from exposure to the triggering stressor.
How does hyrdoxyurea benefit sickle cell patients?
increases fetal hemoglobin.

adverse SE's include bone marrow suppression, leukopenia, anemia, and thrombocytopenia.
Diagnosis of a child who presents with lab values consistent with aplastic anemia, areas of skin hypopigmentation, and poor growth?
Fanconi's anemia - an autosomal recessive disorder believed to involve impaired DNA REPAIR. This dz is marked by progressive bone marrow failure, skin hypopigmentation, morphological abnormalities (such as microcephaly, abnormal thumbs, and hypogonadism), and a predisposition to cancer. The anemia is often MACROcytic and definitive tx for aplastic anemia is a hematopoietic stem cell transplantation.
When does tenosynovial inflammation cause carpal tunnel syndrome?
in the setting of rheumatoid arthritis
When does synovial tendon HYPERPLASIA cause carpal tunnel syndrome?
acromegaly
when does accumulation of FLUID in the carpal tunnel cause carpal tunnel syndrome?
pregnancy especially 3rd trimester.
When does accumulation of matrix substances in the median nerve and tendons cause carpal tunnel syndrome?
hypothyroidism
What can be used to distinguish between portal hypertension and other causes of ascites (trauma, infection, pancreatitis, and malignancy)?
SAAG - the serum ascites albumin gradient.

Subtract ASCITES albumin concentration from SERUM albumin concentration. Difference greater than 1.1 g/dL is consistent with a transudative process i.e. portal hypertension or increased hydrostatic pressure within the liver's capillary beds.
Most common causes of syringomyelia?
Arnold Chiari malformations and prior spinal cord injuries (whiplash of the cervical spine is often an inciting injury).
Mechanism of syringomyelia?
CSF drainage from central canal of the SC is disrupted leading to a fluid-filled cavity that compresses surrounding neural tissue.

Causes decreased strength and diminished pain/temp affecting arms/hands or having a cape-like distribution.
Cervical spondylosis results from?
disc degeneration in patients over 40 years.
How do cutaneous lesions of blastomycosis appear?
either verrucous or ulcerative. Verrucous lesions are initially papulopustular and then progressively become crusted, heaped up and warty with a violaceous hue. These lesions have sharp borders and may be surrounded by microabscesses. Wet preparation of purulent material expressed from these lesions shows the BROAD-based budding yeast form of the organism.
How to distinguish between HSV/VZV retinitis versus CMV retinitis (common in HIV patients)?
HSV/VZV - SEVERE, acute retinal NECROSIS associated with PAIN, keratitits, uveitis, and fundoscopy findings of PALE peripheral and central NECROSIS of the retina.

CMV - More common than HSV/VZV but typically painLESS and NOT associated with keratitis or conjunctivitis. Fundoscopy shows hemorrhages and FLUFFY or GRANULAR lesions around the retinal vessels.
MCC of mitral regurg?
mitral valve prolapse - involves myxomatous degeneration of the mitral valve. Typically causes a pansystolic murmur radiating to the AXILLA but in some cases a midsystolic CLICK can also be appreciated.
Vaccinaton against hepatitis B decreases the incidence of _________, especially in Asia and Africa.
hepatocellular carcinoma

Note: chronic hep B 2dry to vertical mother-to-child transmission is a major cause of hepatocellular CA in Asia and Africa. Contact with infected blood is the major cause in the U.S.
Most common cause of superior vena cava syndrome?
lung cancer - especially small cell and non-Hodgkins lung cancer

other possible causes include fibrosing mediastinitis (2dry to histoplasmosis or TB infection) or thrombosis 2dry to indwelling central venous device.
A biophysical profile score of 4 or less means?
severe fetal asphyxia - deliver immediately if >26 weeks
When is a contraction stress test indicated?
an equivocal non-stress test or biophysical profile
What is a possible negative side effect of using norepinephrine as pressors in hypotensive patients?
norepinephrine-induced vasospasm - it has alpha-1 agonist properties which cause vasoconstriction. This is useful in hypotensive states but can cause ischemia and necrosis of distal fingers/toes in some patients with decreased blood flow. A similar phenomenon can also occur in the intestines resulting in mesenteric ischemia or kidney causing renal failure.
2 important causes of hypOmagnesemia?
chronic alcoholism and diuretic intake
An important cause of refractory hypokalemia?
hypOmagnesemia - Mg is an important cofactor for potassium uptake and maintenance of intracellular potassium levles.
Possible things that can provoke benign intracranial hypertension?
glucocorticoids, vitamin A, and oral contraceptive pills
Difference between bleeding from Mallory-Weiss tears vs esophageal varices?
Mallory-weiss tears - ruptured submucosal ARTERIES

rupture of esophageal varices - rupture of dilated submucosal VEINS

Note: endoscopy will show dilated varices at risk for bleeding whereas mallory-weiss tear is an acute presentation and will not appear until bleeding has started.
Mechanism of radioiodine ablation of thyroid?
taken up by "active" tissue and ablated via beta-emissions.

Since the entire thyroid gland is overactive in Grave's , it is more likely to result in hypOthyroidism whereas multinodular goiter or toxic adenomas end in a euthyroid state usually.
Zinc deficiency?
zinc is digested primarily in the jejunum so results sometimes from malabsorption in IBD or can result from TPN preparations that lack zinc.

Symptoms include alopecia, abnormal taste, bullous/pustulous lesions surrounding body orifices/extremities, and impaired wound healing.
Possible long-term neurologic sequelae associated with BACTERIAL meningitis?
1) hearing loss
2) loss of cognitive functions due to neuronal loss in the DENTATE gyrus of the HIPPOCAMPUS)
3) seizures
4) mental retardation
5) spasticity or paresis
DOC in cachexia related weight loss and anorexia?
progestins such as megestrol acetate and medroxyprogesterone acetate.

Beware of increased risk of DVT however!
antipseudomonal cephalosporins?
ceftazidime and cefepime
How to distinguish between an absence sizure and a complex partial seizure?
absence seizure - hyperventilation during EEG reveals a generalized "SPIKE and WAVE" pattern on a normal background. NO post-ictal state.

complex partial - EEG is usually normal or may show brief discharges but will not respond to hyperventilation. Post-ictal state of confusion common.

Automatisms are common in both types of seizures.
Drugs that may cause folate deficiency leading to megaloblastic anemia?
1) anti-epileptics such as phenytoin, primidone, and phenobarbital by impairing absorption of folic acid in the small intestine
2) TMP and methotrexate by inhibiting dihydrofolate reductase.

Note: most common cause of deficiency is poor diet and/or alcoholism however.
difference btn two-sample t test and a two-sample z test?
both compare two means but the t-test uses a "sample" variance whereas a z-test uses a "population" variance.

Population variances are not usually known, so the t test has more applicability.
Benefits of bronchoscopy in intrapulmonary bleeding?
can simultaneously localize AND control site of intrapulmonary bleeding. Rigid bronchoscopy has the additional benefit of providing good control of the airway.
Medical term for a common staphylococcal abscess of the eyelid?
external hodeolum or stye
First step in management of ALL ELDERLY patients who present with acute renal failure?
Foley catheter due to possible bladder outlet obstruction from BPH - large amount of urine collection from catheter insertion indicates a likely diagnosis of BPH.

Note: bladder outlet obstruction for >2 weeks can result in permanent kidney damage.

Note: first line treatment of BPH withOUT bladder outlet obstruction is alpha-blockers.
What part of the prostate does BPH effect?
the central portion

Prostate cancer effects the Periphery
Principle cause of lacunar strokes?
hypertension leading to thickening of small vessels.

4 common types: pure motor, pure sensory, ataxic-hemiparesis, dysarthria-clumsy hand syndrome
lacunar infarction in the posterior limb of the internal capsule leads to?
a pure motor hemiparesis OR an ataxic-hemiparesis
lacunar infarct of the VPL nucleas of the thalamus leads to?
pure SENSORY stroke
lacunar infarct of the basal pons leads to?
dysarthria-clumsy hand syndrome
Management of INR<5 with no significant bleeding?
omit NEXT warfarin dose
Management of INR 5-9 with no significant bleeding?
stop warfarin temporarily
Management of INR > 9?
stop warfarin, give oral vitamin K
Management of pt with serious bleeding due to excess anticoagulation with warfarin?
give fresh frozen plasma for RAPID reversal of anticoagulation
What should be closely monitored on a DiGeorge pt undergoing surgery?
Ca levels - absence of parathyroid leads to hypOcalcemia which can lead to prolonged QT intervals, laryngeal spasm, convulsions and cramping.
Syncope in a young patient with a murmur at the left sternal border?
likely hypertrophic cardiomyopathy
Suspect what with acute onset severe eye pain and blurred vision (sometimes assoicated with nausea and vomiting) that occured following pupillary dilation (ex. in a darkened movie theater or due to drug intake)?
acute angle closure glaucoma - moderately dilated pupil will be non-reactive to light. Anterior chamber is shallow. Tonometry reveals incr intraocular pressure.

Tx with IV acetozolamide with subsequent oral administration. Permanent cure is offered with laster peripheral irodotomy.

Note: open angle glaucoma has a more insidious onset with gradual loss of peripheral vision resulting in tunnel vision. May also feature persistently increased intraocular pressure and pathologic CUPPING of the optic disc.
What can happen with an eschar that develops due to a burn?
it can naturally slough off or require surgical debridement because it begins to compromise both blood and lymph circulation. In these cases, doppler sono is used to document peripheral pulses and estimate tissue compartment pressure. A pressure of 25-40 is the threshold to perform escharotomy.
Diagnosis of blisters that show IgG and C3 deposits linearly along basement membrane (that target HEMIdesmosomes)?
Bullous pemphigoid - often triggered by culpit meds like furosemide, NSAIDS, captopril, pecillamine, and various ABX. Skin findings include TENSE bullae, urticarial plaques, and pruritus.

Note: blisters of pemphigus are INTRAepidermal with IgG deposits BETWEEN epidermal cells that target the DESMOGLEINS. Bc these blisters form at a more superficial layer of the skin, they tend to be more flaccid and fragile than bullous pemphigoid.
Somatization disorder:
MULTIPLE recurrent somatic complaints that have persisted for several years and been evaluated by many to no avail.

Requires at least 4 PAIN symptoms, 2 GI symptoms, sexual OR reproductive symptoms other than pain, and 1 PSEUDONEUROLOGICAL symptom such as blindness, deafness, weakness, seizure, loss of consciousness or impaired balance.
2 causes of hypocalcemia with CONCORDANT changes in phosphate levels (hypophosphatemia)?
1) Vitamin D deficiency (e.g. due to malabsorption)
2) acute pancreatitis
Hypocalcemia due to albuminemia is unique because?
there are NO symptoms of hypocalcemia (bc ionized Ca levels remain unchanged).
Solid ovarian tumors (viewed by ultrasound) are almost always malignant and demand immediate and aggressive evaluation/treatment in ALL age groups EXCEPT one scenario which is?
pregnancy! they are most likely pregnancy luteomas which appear BILATERAL, multinodular, SOLID masses on both ovaries bc of luteinized stromal cells from the influence of hCG. Common in AA multiparous women and 1/3 will develop sudden onset hirsutism/virilization.
Which type of tumor (infra or supra-tentorial?) are most common in the pediatric population?
infratentorial (60%)
supratentorial (25%)

benign ASTROCYTOMAS are the most common histologic type in BOTH groups.
A major cause of blindness WORLDwide?
Trachoma caused by Chlamydia trachomatis serotype A-C. Often CONCURRENT infection of the NASOPHARYNX. Look for FOLLICULAR conjunctivitis and pannus (NEOVASCULARIZATION) in the cornea.
Most common nerve injury in association with fracture of the midshaft humerus?
radial nerve - leads to wrist drop and/or marked limitation of extension at wrist joint
Extrahepatic complaints/sequelae of chronic hepatitis C?
arthralgias (may be false-positive rheumatoid factor), myalgias, cryoglobulinemia, porphyria cutanea tarda, and glomerulonephritis.
How to distinguish between herpes simplex keratitis versus herpes zoster ophthalmicus?
herpes simplex keratitis - dendritic ulcers are the most common presentation with epithelial scrapings that show multi-nucleated giant cells. Usually precipitated by sun exposure or outdoor activities, fever, or immunodeficiency. Hx of prior episodes present.

Herpes zoster ophthalmicus -caused by varicella-zoster. Most episodes in the ELDERLY. Presents with a vesicular rash in the distribution of the cutaneous branch of the first division of the trigeminal nerve. Conjunctivits and ulcers seen in eye.
Marfan's features + mental retardation + thromboembolic events (e.g. stroke) + DOWNward dislocation of the lens =
homocystinuria caused by errors in methionine metabolism 2dry cystathionine synthase deficiency - tx involves high doses of Vitamin B6.
Sudden onset of photopsia (flashes of light) and floaters (spots in the visual field)?
retinal detachment with classic description of "a curtain coming down over my eyes." Usually inciting event occurs months before and is some type of trauma. Fundoscopy shows GREY, elevated retina

Note: central retinal artery occlusion also presents with sudden painLESS loss of vision but fundoscopy shows pallor of the optic diisc, cherry red fovea, and boxcar segmentation of blood int he retinal VEINS.
Common meds that cause hyperkalemia?
ACE-I, spironolactone, and TMP
Diagnosis in thromboctyopenia and hypercoagulation within days of initiating anticoagulation therapy?
HIT - vascular thrombosis in 50% of patients - will show a prolonged aPTT.
Surgical excision of what kind of tumor can cause facial droop? (presents as a firm, nontender swelling of the cheek and fullness of the parapharyngeal space)
parotid gland neoplasm bc the two lobes of the parotid gland are separated by the facial nerve.
Hoarseness can result from injury to the recurrent laryngeal branches of the vagus nerved during what type of surgery?
surgery on the thyroid or parathyroids
what is tic douloureux?
trigeminal neuralgia
hypoglossal nerve injury causing tongue palsy may result from surgical excision of this kind of tumor?
submandibular salivary gland tumor (or any tumor below the mandible).
What test best EXCLUDES a pulmonary embolism?
a negative D-dimer bc it has a 95% negative predictive value
How long should warfarin be continued in a VTE?
6 months in a 1st-time clot, lifetime with a 2nd episode
gold standard for evaluating peripheral artery disease?
contrast arteriography however it is used less frequently bc it is more invasive. Sono is first imaging of choice.
Treatment for Candida vulvovaginits?
oral fluconazole OR
TOPICAL nystatin
Suspect what when an MRI shows MULTIPLE demyelinating, NON-enhancing lesions with NO mass effects in patient with advanced HIV?
Progressive multifocal leukoencephalopathy - no treatment; mean survival is 6 months from time of diagnosis

Note: cerebral toxoplasmosis shows multiple ring-ENHANCING lesions on MRI
What are Howell Jolly bodies?
nuclear remnants within RBCs typically removed by the spleen. Their presence strongly indicates physical or functional asplenia. Seen as single, round, blue inclusions on Wright stain.

Note: do not confuse with Heinz bodies which are hemoglobin precipitants and may also appear blue to violet.
Major source of protein in human milk?
whey which is more easily digested than casein and helps to improve gastric emptying.

breast milk has an INadequate supply of vitamin D and should be supplemented to exclusively breast fed infants.
A NEW fourth heart sound is a classic finding for?
MI - ischemic damage leads to diastolic dysfunction and a stiffened left ventricle --> atrial kick or "gallop"
Suspect what in an infant born with a small body size, microcephaly, DIGITAL/NAIL hypOplasia, midfacial hypoplasia, hirsutism (excess hair), cleft palate, and rib abnormalities?
fetal hydantoin syndrome from anticonvulsant meds such as phenytoin or carbamazepine.
What is the most probable cause of a patient experiencing "floating spots" and blurred vision in one eye AFTER a penetrating injury to the opposite eye several weeks prior?
Sympathetic ophthalmia aka "spared eye injury" - caused by uncovering of "hidden" antigens during a penetrating injury. Once these natural barriers are broken, an immune response against these antigens can result in the healthy (sympathetic) eye.
Dx with >25% lymphoBLASTS that LACK peroxidase positive granules but CONTAIN cytoplasmic aggregates of PAS positive material? Immunostaining for terminal deoxynucleotydyltransferase (TdT) is also usually positive (expressed by pre B and pre T lymphoblasts).
ALL
When is Winter's formula used?
To estimate how much pCO2 should decrease to compensate for a metabolic acidosis (i.e. bicarb decrease).

pCO2=1.5[HCO3] + 8
In which type of arthritis is morning stiffness > 1 hour?
RA
Why is it well documented that rheumatoid arthritis patients are at increased risk of developing osteopenia and osteoporosis?
Due to the combined effects of the dz process itself, glucocorticoid therapy, predilection for female sex, and decreased ability to perform weight-bearing exercises that prevent osteoperosis.
What is another name for osteitis deformans?
Paget's dz
Cause of osteitis fibrosis cystica (Von Recklinghausen disease) ?
hyperparathyroidism - when osteoclastic resorption of bone leads to replacement iwth fibrous tissue (brown tumors).
Suspect what in a pt with recurrent kidney stones since childhood, a positive family hx, a positive urinary cyanide nitroprusside test, and urinalysis that shows hexagonal crystals? Stones are hard and radioopaque.
Cystinuria - an inherited dz due to impaired amino acid TRANSPORT. Problem lies with defective transport of dibasic amino acids (cystine, lysine, arginine, and ornithine) by brush borders of renal tubular and intestinal epithelial cells. Cystine is poorly soluble in water leading to hard, radioopaque renal stones. The urinary cyanide nitroprusside test detects elevated cystine levels!
3 main categories of diabetic retinopathy?
1) backround or simple (usually asymptomatic) - microaneurysms, hemorrhages, exudates, retinal edema
2) pre-proliferative - cotton wool spots
3) proliferative or malignant - neovascularization

Note: visual impairment occurs with the development of MACULAR EDEMA. Argon laster photocoagulation is performed for the prevention of complications.
Risk factors for a polyp to progress to a malignancy?
1) VILLOUS compartment
2) sessile (most villous adenomas are sessile, not pedunculated)
3) > 2.5 cm in size
Recommendation for pneumococcal vaccine?
1) 1 dose for ALL healthy adults >65
2) 1 dose for adults <65 wiht chronic medical conditions plus a BOOSTER 5 years later
Next step in management of a CT scan that reveals a complex loculated effusion with a thick surrounding peal in the pleural space? (A chest tube is placed with little drainage).
empyema - infection of the pleural space. Old residual blood is an excellent medium for bacterial growth and pt will present with fever. Best diagnosed with CT scan and SURGERY is best treatment. Thick pleural peel is removed, pus removed, and chest drained.
Cholecystectomy is indicated in what patients?
ALL patients with SYMPTOMATIC gallstones who are medically stable enough to undergo surgery.
What does a prolonged QRS interval suggest?
a bradyarrhythmia
What does a prolonged QT interval suggest?
a tachyarrhythmia
Why are blood cultures and cultures from cutaneous pustules (usually from the extremities) usually negative?
The specific strain of N. gonorrhoeae that causes this disseminated form of infection has very specific growth requirements. Dissemination is most likely to occur during menstrual periods.
How can invasive aspergillosis (almost always in immunocompromised patients) be diagnosed?
CXR will show a rapidly rogressive dense consolidation.

CT scan will show pulmonary nodules with a HALO SIGN or lesions with an AIR CRESCENT.
What kind of bias does a loss to follow- up cause?
selection bias
3 possible Schilling test results:
1) normal urinary excretion of radiolabeled B12 - suggests normal absorption and excretion of by the kidney
2) Diminished urinary excretion of radiolabeled Vit B12 --> pernicious anemia OR malabsorption
a) Normal excretion AFTER addition of intrinsic factor --> pernicious anemia
b) LOW excretion AFTER addition of intrinsic factor --> malabsorption
A PERSISTENT cough with elevationo f the left main stem bronchus may suggest?
mitral stenosis - left atrium gets very large and tends to push up on the left main stem bronchus. Irritation on the left main stem (and phrenic nerve) by the enlarged left atrium can produce a persistent cough.
What should be suspected in smokers who present with Horner's syndrome?
lung cancer until proven otherwise - 1st step in mgmt is a CXR
DOC in hairy cell leukemia?
cladribine
What type of neuropathy is expected in diabetes?
SYMMETRIC DISTAL sensorimotor polyneuropathy characterized by the classic "stocking glove" pattern of SENSORY loss.

Type of sensory involvement depends on the type of nerve fibers involved. PURE SMALL fiber neuropathy results in more pain, allodynia, and parestheisas with ankle jerks PRESERVED. PURE LARGE fiber neuropathy results in less pain but MORE NUMBESS with pressure, proprioception and vibratory sensations DECR and LOST ankle jerks.
What does a "corkscrew" esophagus on barium swallow suggest?
diffuse esophageal spasm
What might a manometry show of an esophagus in scleroderma?
loss of DISTAL peristalsis of the esophagus and a lower esophageal sphincter that is INCOMPETENT (i.e. low tone).
Drugs of choice for fibromyalgia?
Amitriptyline with goal of increasing the amount of restorative phase 4 sleep. Cyclobenzaprine can be used in a similar way.

Note: If pt had concurrent depressive symptoms, begin SSRIs as well.
Most common bone in the body to be affected by stress fractures?
classic locations:
1) anterior part of hte MIDDLE third of the tibia in jumping sports
2) POSTEROmedial part of the DISTAL third of the tibia in runners.

Note: XR is usually normal. Use a CT or bone scan to evaluate.
What should be suspected in ANY postpartum woman with pulmonary symptoms and multiple nodules on CXR?
choriocarcinoma - may occur after molar pregnancy or NORMAL GESTATION or abortion. Irregular vaginal bleeding beyond 8 weeks post-partum should raise suspicion for this Dx.

Obtain hCG for Dx.
Most common cause of painless hematuria in adults?
Bladder tumors

Note: erythrocytes in urine should also be confirmed microscopically bc gross red urine may also occur in myoglobinuria, hemoglobinuria, porphyria, following the consumption of a large amount of beets or as an adverse effect of certain meds like rifampin.
What does a triad of systemic vasculitis, upper/lower airway granulomatous inflammation, and glomerulonephritis suggest?
Wegener's granulomatous - UPPER respiratory tract is most common site of involvement with epistaxis, purulent rhinorrhea, otitis, sinusitis, and over time a saddle nose deformity. Cutaneous manifestations can include painful subQ nodules, palpable purpura and/or pyoderma gangrenosum-like lesions.

Lab tests usually demonstrate a positive C-ANCA due to antiboidies against proteinase-3 and an elevated CRP. Urinalysis shows RBC casts, proteinuria, and sterile pyuria if glomerulonephritis is present. Tx is with CYCLOPHOSPHAMIDE.
The most distinctive feature of MEN type 2b?
mucosal neuromas (present in more than 90% of cases) and MARFANoid habitus.
The most distinctive feature of MEN type 2a?
primary hyperparathyroidism due to parathyroid HYPERPLASIA not adenoma.
the 3 Ps in MEN type?
MEN type 1:
Pituitary adenoma
hyperParathyroidism
Pancreatic islet cell tumor
The 2 Ps in MEN type?
MEN type 2a:
medullary thyroid cancer
Pheochromocytoma
Primary parathyroid hyperplasia
The 1 P in MEN type?
MEN type 2B:
Medullary thyroid cancer
Pheochromocytoma
Mucosal neuromas and Marfanoid habitus
Bilateral breast tenderness and swelling that typically presents 24-72 hours post-partum, peaks 3-5 days after delivery and resolves spontaneously?
breast engorgement
Management of a sickle cell child with probable stroke?
exchange transfusion - decr percentage of sickle cells and prevents a second infarct from occurring. Stroke is 2dry to sludging and occlusion in the cerebral vasculature.
Treatment for atrophic vaginitus in post-menopausal wmen?
LOCAL estrogen therapy

Note: UTI can present with similar symptoms so rule out!
Treatment for the 10-20% of pts on isoniazid that develop mild aminotransferase elevations within first few weeks of tx?
As long as levels are <100 IU/L, do nothing except regularly monitor for further elevations.
Testing for what serologica markers off ther best SCREENING for acute hepatitis B?
HBsAg and IgM anti-HBc
investigation of choice to diagnose an intraabdominal abscess?
CT scan - such infections are usually from hematogenous spread from the skin, commonly due to S. aureus
First line treatment for otitis media?
10 day course of amoxicillin - if regimen fails, amoxicillin-clavulanic acid, cefuroxime axetil, and IM ceftriaxone are good alternatives.
Triad of polyarthralgias, tenosynovitis, and vesiculopustular skin lesions suggests?
disseminated gonoccal infection

Note: all patients with this finding should undergo HIV screening
DOC for nocardiosis?
TMP-SMX - common in patients with deficient cell-mediated immunity. Can present with pulmonary, CNS, or cutaneous manifestations. 1/3 will have empeyema, 1/2 will have EXTRA-pulmonary dissemination (brain being most common).

Sputum gram stain shows crooked, branching, beaded, gram-positive and partially acid-fast filaments
CSF of a multiple sclerosis patient will show?
oligoclonal bands in 85-90% of cases
A large number of molluscum contagiosum lesions should rise suspicion for?
HIV unless explained by some other type of cellular immunodeficiency such as chemotherapy or corticosteroid use.
A mid-diastolic rumbling PLUS the presence of a mass in the left atrium indicates?
Either a thrombus or an intracardiac tumor. Constitutional complaints of low-grade fevers and weight loss make a tumor more likely.
Most common diabetic MONOneuropathy?
somatic component of CN III causing a "down and out" gaze due to ISCHEMIA.

Parasympathetic fibers have a separate blood supply so light and accomodation reflexes remain intact.
Best form of treatment for molluscul contagiosum?
Curettage or application of liquid nitrogen.
Acute, MASSIVE increases in the AST and ALT with milder increases in the total bilirubin and ALP with a setting of hypotension indicates?
ischemic hepatic injury - if the patient survives the inciting condition, liver enzymes should return to normal within 1-2 weeks.
Metabolic acidosis with BOTH an anion gap and an osmolar gap indicates possible?
ethylene glycol, methanol, or ethanol intoxication
rectangular, EVELOPE-shaped crystals are seen in?
ethylene glycol poisoning (antifreeze) - these are calcium oxalate crystals
Calculation for serum osmolality?
2Na + Glu/18 + BUN/2.8
Anti-mitochondrial antibodies indicate?
primary biliary cirrhosis - disappearing bile duct dz due to autoimmune destruction - pruritus is usually the first symptom and may be very severe especially at night.

DOC=Ursodeoxycholic acid (slows dz progression)

Definitive treatment is liver transplantation.
Most specific arrhythmia for digitalis toxicity?
atrial tachycardia with AV block - digitalis causes increased ectopy in hte atria or ventricles. It can also increase vagal tone and decr conduction through the AV node, potentially causing AV block.
How to distinguish atrial tachy from atrial flutter?
Atrial tachy has a somewhat slower rate - 150-200 vs. 250-350 bpm in flutter. P-waves are also present but may appear different from normal p-waves.
SIADH is commonly associated with what type of cancer?
Small cell carcinoma of the lung
Common symptoms of stimulant (cocaine, amphetamine) INTOXICATION?
Psychosis (more common with amphetamines), DILATED pupils, hypertension, and tachy.
Unexplained fever and cough in an HIV patient with CD4 count < 50/mm3 with no past hx of or exposure to tuberculosis is suspicious for?
Mycobacterium avium - pts with CD4 count < 50 should receive azithromycin as prophylaxis.
increased hCG and AFP in a young male is indicative of?
a NONseminomatous germ cell tumor of the MEDIASTINUM.

Note: elevation of ONLY hCG with normal AFP indicates a seminomatous germ cell tumor.
Immediate management of gastroschisis versus omphalocele?
the same - wrap exposed bowel in sterile saline dressing and plastic wrap to minimize heat/fluid losses.

gastroschisis look "angry" and matted, is NOT covered by a membrane, and is NOT associated with other abnormalities.

Omphalocele is herniation that IS covered by a membrane and IS associated with OTHER congenital abnormalities.
Treatment for actinomycosis?
high-dose penicillin for 6-12 weeks.

Presents as slowly progressive, non-tender indurated mass which evolves into multiple abscesses, fistula, and draining tracts with sulfur granules which appear YELLOW.
Treatment for moderate-to-severe acne that is predominantly nodulocystic and to those who have developed scars?
ORAL isotretinoin
Urinary urgency, frequency, and nocturia plus chronic pelvic pain that is exacerbated by sexual intercourse,filling of the bladder, exercise, spicy foods, and certain beverages is suspicious for?
interstitial cystitis aka painful bladder syndrome
How should carotid artery stenosis of 60-99% in ASYMptomatic men be treated?
carotid endarterectomy - men with lesions greater than 80% benefit the most.
Status epilepticus is defined as seizure activity greater than?
5-10 minutes that does not respond to 1st line treatment with benzodiazepines. In these cases, first step in management is secure airway. Then try 2nd line antiseizure medication.
linear IgG antibodies against alpha-3 chain of type IV collagen along the glomerular and alveloar basement membranes?
Goodpasture's
what type of organism is most common in a UTI that causes ALKALINE urine?
Proteus
The preferred form of hormonal contraception for lactating mothers?
progestin-only

note: combined estrogen-progestin pills may DECR milk production and pass into the milk
What type of patients have a 10% per year risk of experiencing reactivation tuberculosis?
HIV patients.
How to distinguish a Chlamydial pneumonia versus RSV bronchiolitis in a young infant?
Chlamydia pneumonia usually does NOT have FEVER and WHEEZING is RARE.
The most important changes necessary to reducing blood pressure?
Weight control is most important followed by physical activity, salt restriction, and moderation of alcohol consumption.
How does Zollinger-Ellison syndrome lead to malabsorption?
it is a gastrin producing pancreatic tumor that causes parietal cell hyperPLASIA --> significantly increased stomach acid production --> increased stomach acid INACTIVATES pancreatic enzymes --> fat malabsorption and steatorrhea
An over the counter drug that has potent anticholinergic effects that may cause eye and oropharyngeal drynesss as well as urinary retention (2dry to detrusor inactivity), especially in older males who may have some underlying BPH?
first-generation H1 antihistamines such as diphenhydramine, chlorpheniramine, doxepin, and hydroxyzine
How to distinguish between CHF versus COPD exacerbation?
Both will show hypoxia.

COPD - pts will retain CO2 (hypERcapnia) and be in respiratory ACIDOSIS.

In CHF pts will blow off CO2 (hypOcapnia 2dry to hyperventilation) and have respiratory ALKALOSIS.
Pulmonary hypertension is defined as?
mean pulmonary arterial pressure greater than 25 mmHg at rest or 30 mmHg with exercise.
A tea and toast type of diet is associated with what type of anemia?
macrocytic anemia due to folic acid deficiency

Note: B12 stores remain sufficient for at least 3-4 YEARS whereas folic acid stores can become depleted within 4-5 months
What type of metals in jewelry can cause a contact dermatitis?
nickel
Retinal hamartoma versus optic glioma in what neurocutaneous syndrome?
retinal hamartoma in tuberous sclerosis.

optic glioma in neurofibromatosis type 1.
common drugs that cause priapism?
prazosin and trazodone
Criteria to diagnose a MASSIVE pulmonary embolism?
right atrial pressure > 10

pulmonary artery systolic pressure > 40

Note: massive PE can lead to symptoms of shock such as hypotension, tachycardia, and cool extremities.
normal RIGHT atrial pressures
4-6 mmHg
normal pulmonary ARTERY pressure
does not exceed 25/15
normal PCWP?
6-12 mmHg
dx of infant with pruritus and skin lesions typically distributed symmetrically over the face, scalp, chest, and extensor surfaces of the extremities but SPARING the diaper region?
atopic dermatitis
Clues to Boerhaave's syndrome?
1) acute, severe chest or epigastric pain after an episode of retching
2) tachycardia and tachypnea
3) subcutaneous or mediastinal emphysema
4) WIDENED mediastinum
5) UNILATerally decreased breath sounds
6) UNILATeral pleural effusion (usually left)
7) HIGH AMYLASE concentration in pleural fluid
Acute treatment of hypercalcemia?
IV saline hydration followed by a loop diuretic to decrease calcium reabsorption by the loop of Henle
Symptoms of hypercalcemia usually begin when Ca levels exceed?
12 mEq/L

symptoms are nonspecific like abdominal pain, constipation, polyuria and neuropsychiatric disturbances.
B-cell deficiencies predispose to infection by?
bacteria
T-cell deficiencies predispose to infection by?
viruses and fungi
Recurrent infections after passing 6 months of age is suggestive of?
GENETIC B-cell deficiencies bc this is when the level of maternal antibodies drop.
2 forms of analgesic nephropathy?
papillary necrosis and chronic tubulointerstitial nephritis.
Early versus late manifestations of analgesic nephropathy (papillary necrosis and chronic tubulointerstiital nephritis)?
early - polyuria, sterile puria, and sometimes WBC casts. Microscopic hematuria and renal colic following sloughing of renal papilla.

later - hypertension, mild proteinuria, and impaired urinary concentration.

severe - nephrOtic range proteinuria

Note: Pts with chronic analgesic abuse are more likely to develop premature aging, atherosclerotic vascular disease, and urinary tract CANCER.
3 types of PARTIAL seizures:
simple: NO loss of consciousness and patient remembers the event well.

complex: +LOC, AURA present (=simple partial seizure), automatisms (lip smacking, chewing, hand movements).

with 2dry generalization: +LOC, AURA present, TONIC CLONIC activity

Unwitnessed seizures with presence of tongue biting or bladder/bowel incontinence makes seizure with tonic clonic activity more likely (so partial with 2dry generalization or generalized seizures).
Lennox-Gastaut syndrome
seizure disorder where patients are younger than 7 with coexisting mental retardation.
congenital AROMATASE deficiency?
total absence or poor functioning conversion of androgens into estrogens:

IN UTERO, lack of estrogen leads to masculinization of the mother and virilized XX fetuses with ambiguous external genitilia but normal internal genitilia.

LATER IN LIFE, patients present with delayed puberty, primary amenorrhea,osteoporosis, UNDETECTABEL circulating estrogens, high concentrations of gonadotropins and polycystic ovaries.

Note: congenital adrenal hyperplasia causes virilization in XX fetuses too, as well as salt wasting.
How can you distinguish from psychogenic polydipsia versus diabetes insipidus?
water deprivation test - urine WILL CONCENTRATE if proper levels of ADH present, which indicates a psychogenic problem
How do you distinguish between central DI and nephrogenic DI?
First, do a water deprivation test, and make sure the patient canNOT concentrate urine.

2nd, administer arginine vasopressing or desmopressin. If urine now CONCENTRATES, it indicates a lack of CENTRAL release. If it does NOT concentrate, it indicates that renal tubules are resistant to the hormone.
Less well known side effects of amiodorone?
corneal deposits (bc secreted by the lacrimal gland) and a blue-gray skin discoloration (most prominent on the face).
Test of choice for diagnosing a suspected ectopic pregnancy with b-hCG levels between 1,500-6,500?
transVAGINAL ultrasound - if ultrasound fails to reveal an intrauterine OR adnexal sac in this setting, then SERIAL beta-hCG measurements are necessary to rule in/out ectopic pregnancy. Doubling of b-hCG every 48 hours suggests a normal pregnancy, and a slower rate of rise suggests an ABNORMAL pregnancy.
Hepato-jugular reflex is ________ in patients with liver disease related edema.
negative

it is positive in heart related edema and indicates elevated venous pressure.
What kidney pathology is associated with cerebral aneurysms and a positive family hx of stroke/sudden death?
polycystic kidney disease
What kind of arthritis classically features morning stiffness, involves DIP joints, dactylitis ("sausage digits"), nail pitting, and onycholysis (separation of nail bed)?
psoriatic arthritis

tx = NSAIDs, anti-TNF agents, and methotrexate

Note: systemic corticosteroids are relatively contraindicated.
What kind of arthrits is common in diabetics, syphilis, and alcoholism?
Neuropathic arthropathy (Charcot joint) - most commonly affects the lower limbs. Peripheral neuropathy is believed to result in decreased proprioception which leads to frequent trauma and eventual destruction of the joint.
What should be suspected in an elderly lady with severe osteoporosis who presents after a fall with bilateral leg weakness, increased deep tendon reflexes, and low back pain?
compression fracture with disk herniation causing spinal CORD COMPRESSION. no other SINGLE lesion would explain bilateral leg weakness. Can also occur due to an abscess, trauma, or malignancy.

Note: other related clues might include saddle anesthesia or compromised bladder/bowel control.
Atelectasis is the most common respiratory complication during the first 24 hours after surgery due a fall in vital capacity (by 50%) and decreased functional residual capacity (by 30%). What 5 methods can help increase the FRC and prevent atelectasis in the immediate postop period?
1) chest physiotherapy
2) incentive spirometry
3) coughing
4) frequent repositioning - simply moving the pt from supine to sitting reduces the intrabdominal pressure acting on the undersurface of the diaphragm thereby permitting greater alveolar expansion at end expiration and increasing the FRC.
5) EARLY ambulation
What cellular mechanism is responsible for TCA-induced QRS prolongation (> 0.10 seconds)?
inhibition of cardiac FAST SODIUM channels is responsible for QRS prolongation. This is reversed by sodium bicarbonate in instances of intoxication.

Note: urine alkalinazation is a mechanism by which sodium bicarbonate increases salicylate secretion, thus alleviating aspirin overdose.
Steps in management of variable decelerations of FHR?
variable decels represent a non-reassuring fetal heart pattern due to umbilical cord compression. Management should be:
1) oxygen administration and have mother lie on her side
2) if variable decels persist, pt should be placed in the Trendelenburg position and the presenting fetal part should be elevated.
3) Persistent variable decels may require amnioinfusion into the amniotic cavity but should be used after conservative measures have failed.
Most appropriate management of progressive pain in a patient with prostate cancer and vertebral bone metastases after androgen ablation (orchiectomy)?
radiation therapy
Otoscopic finding of granulation tissue in the external auditory canal is consistent with?
malignant otitis externa - usually seen in elderly patients with poorly controlled diabetes and presents with ear pin, drainage, and granulation tissue. Can be exacerbated with chewing in early stages and ivolves the cranial nerves sometimes.

DOC=IV ciprofloxacin (due to anti-psuedomonal coverage).

Note: this is an external ear infection but requires SYSTEMIC therapy.
Differential for bloody diarrhea but no travel?
1) EHEC - no fever but ABDOMINAL pain.
2) Shigella, salmonella, or campylobacter - FEVER but NO abdominal pain.

Note: viral gastroenteritis usually results in VOMITING and DIARRHEA
Possible hematological complication that may occur with infectious mononucleosis?
autoimmune hemolytic anemia and thrombocytopenia - this is due to the CROSS reactivity of the EBV-induced antibodies against red blood cells and platelets. These antibodies are IgM COLD agglutinin antibodies aka anti-i antibodies.

Note: onset of hemolytic anemia can be 2-3 weeks after the onset of symptoms.
Definition of intracranial hypertension?
intracranial pressure >/= 20 mmHg. Typical symptoms include diffuse headaches that tend to be worse in the morning, nausea and vomiting early in the day, vision changes, papilledema, cranial nerve deficits, somnolence, confusion, unsteadiness, and Cushing's reflex (HTN and bradycardia). Etiologies include trauma, space-occupying lesions, hydrocephalus, and impaired CNS venous outflow.

CT and MRI can help diagnose this.
Prodrome of fever, irritability and skin tenderness is followed by generalized erythemy and superficial flaccid blisters with a positive Nikolsky sign. Scaling and desquamation follow, before resolution of the disease process. Usually affects children below age 10 but adults with kidney disease or immune compromise may also be affected.
Staphylococcal scalded skin syndrome caused by exfoliative toxin-producing strains of S. aureus.
Screening for ovarian cancer in patients with positive family history?
Testing for BRCA1 and BRCA2 genes could be condsidered if positive family history is VERY strong. However, NO screening is officially recommended for ovarian cancer. If BRCA1/BRCA2 genes are positive, follow up CA 125 and pelvic ultrasound to look for ovarian cancer should be performed.
Post exposure prophylaxis for possible rabies from dog?
immediat prophylaxis for exposures involving head or neck or if status of animal cannot be determined (then it is assumed that dog is RABID).

Otherwise, observe dog for 10 days and give prophylaxis if features of rabies within dog manifests.
Treatment for diphenhydramine overdose?
physostigmine
Recommended screening for abdominal aortic aneurysm?
active or former male smokers aged 65-75 years with a one-time abdominal ultrasound to evaluate for abdominal aortic aneurysm.
Management of communicating versus non-communicating hydroceles?
Most cases of both types of hydrocele will spontaneously resolve by age 12.
Symptomatic sarcoidosis most commonly presents with?
cough, erythema nodosum, anterior uveitis, and arthritis.

Hilar adenopathy and reticular opacities on CXR are classic findings.
The relative risk (RR) can help determine what percent of an "exposed" population with a "given" disease is actually ATTRIBUTABLE to that exposure. Referred to as attributable risk percent (ARP).
ARP=(RR-1)/RR
Management of a painLESS, hard testicular mass PLUS ultrasound suggestive of tumor?
orchiectomy - removal of the testis and its associated cord
Procedure of choice for both diagnostic and therapeutic purposes in suspected foreign body aspiration?
direct laryngoscopy and RIGID bronchoscopy.

Flexible bronchoscopy is useful for diagnosis but NOT retrieval of the foreign body.
Most accepted and recommended management for the eradication of H. pylori in patients with gastric mucosa-associated lymphoid tissue lymphoma withOUT metastasis?
antibiotic therapy - give combo of omeprazole, clarithromycin and amoxicillin
Management of patients who present after >5 days after the onset of symptoms of appendicitis and have localized right lower quadrant findings?
IV hydration, antibiotics and rest. Antibiotics should cover enteric gram-negative organisms and anaerobes. Cefotetan is adequate monotherapy.
Treatment for myasthenia crisis?
endotracheal intubation and withdrawal of anticholinesterases for several days.

Typical cause for myasthenic crisis is an intercurrent infection and so antibiotics are an important part of management.
Paget's dz is often asymptomatic and usually found incidentally by x-ray findings like FEMORAL BOWING or ELEV ALP. Symptoms when present may include?
skeletal deformities, bone or joint pain, fractures, nerve entrapment (especially cranial nerve 8 leading to hearing loss), or osteosarcoma.
The single most common cause of asymptomatic isolated elevation of ALP in an elderly patient?
Paget's disease of bone (osteitis deformans)
Suspect ________ in a child who recently recovered from a diarrheal illness and presents with acute renal failure, microangiopathic hemolytic anemia, fever, thrombocytopenia, and characteristic peripheral smear finding of schistocytes?
HUS
Management of hyperthyroid-related atrial fibrillation?
beta blocker, not cardioversion (unless hemodynamically unstable or shows signs of angina or heart failure).
Mechanism behind autoimmune hemolytic anemia in malignant lymphoproliferative disorders like CLL?
due to anti-red blood cell IgG immunoglobulins of the WARM type covering the cell membranes and causing removal from the circulation by the spleen.

Treatment is PREDNISONE in divided doses and if INeffective, then splenectomy.
Current recommendations to prevent complications from splenectomy?
pts should receive anti-pneumococcal, Haemophilu, and meningococcal vaccines several weeks before the operation and DAILY oral penicillin for 3-5 years following splenectomy. Thereafter, at home antibiotics should be made available for immediate treatment of any signicant fever.
Hypercalcemia can occur following __________ in patients with preEXISTING HIGH bone turnover such as children, young adults, and patients with Paget's disease.
immobilization - bisphosphonate therapy is helpful in reducing hypercalcemia and preventing osteopenia.
Handling of amputated parts from injury?
wrap in saline-mostened gauze, seal in a plastic bag, and place on ice to bring with to emergency department.
Superior sulcus tumor can compress various areas leading to symptoms:
1) sympathetic trunk (Horner's)
2) brachial plexus (Pancoast syndrome)
3) right recurrent laryngeal nerve (hoarse voice)
4) superior vena cava (SVC syndrome)

Note: Pancoast syndrome is usually shoulder pain radiating into the arm in an ulnar distribution. Caused by tumor invasion of C8 and T1.
Among what population is pellagra common?
People eating CORN-based diets in parts of INdia, Africa, and China as well as alcoholics, carcinoid syndrome, and Hartnup's dz.

Note: Diarrhea, dementia, dermatitis and eventually death.
Signs common in exertional heat stroke?
body temp > 105 which can also cause rhabdomyolysis and organ system damage. Large blood with NO RBCs on U/A is suggestive of rhabdo. Also, dry skin/mucosa, hypOtension, tachycardia, tachypnea.
definition of fulminant liver failure?
hepatic encephalopathy that develops wi 8 weeks of the onset of acute liver failure - more common in pts who are heavy users of acetaminophen, alcohol, methamphetamines, or coinfected with hepatitis B & D.
Management of fulminant hepatic failure?
Liver transplantation bc these pts have a mortality rate > 80%. Contraindications for transplantation include IRREVersible cardiopulmonary dz, incurable or recent (<5 years) malignancy external to the liver, and ACTIVE alcohol/drug abuse.
Management of an unvaccinated individual with needle stick exposure from a patient with active hepatitis B?
administration of both Hep B vaccine as well as immune globulin.

If vaccinated, then immune globulin is sufficient.
Why is hyperkalemia in the setting of diabetic ketoacidosis referred to as "paradoxical"?
bc body potassium reserves are actually depleted!
Sudden loss of vision and onset of floaters with a fundus that is hard to visualize in a diabetic patient?
vitreous hemorrhage - difficult to visualize fundal details is an important clue!
Absolute contraindication to the use of bupropion?
history of seizure disorder
First step in management of primary biliary cirrhosis?
ursodeoxycholic acid - relieves symptoms and lengthens transplant-free survival time.

methotrexate and colchicine have also been shown to be of moderate benefit.
Increased homocysteine levels PLUS increased levels of methylmalonic acid indicate?
cobalamin deficiency - bc this is not only necessary for conversion from homocysteine to methionine but also for conversion from methylmalonyl-CoA to succinyl-CoA.
Increased homocysteine levels but NOT methylmalonic acid?
folic acid deficiency bc it is required in conversion from homocysteine to methionine but not for conversion of methylmalonyl-CoA to succinyl-CoA.
What medications are contraindicated in acute glaucoma?
meds that cause mydriasis such as atropine.

Mannitol, acetazolamide, pilocarpine, or timolol can be used for acute glaucoma tx.
Treatment for pheochromocytoma paroxysms?
NEVER beta-block without adequate ALPHA-block FIRST. Blocking beta-receptors leads to unopposed stimulation of vascular alpha-receptors which can result in rapid, catastrophic rise in BP.

Therefore, alpha-blockers are preferred initial drugs. Beta-blockers can be added to treat tachycardia and other symptoms of sympathetic hyperactivity like tremor but only after adequate alpha block is in place. Non-selective blockers such as labetelol can be used safely as initial treatment.
How is pH helpful in evaluating parapneumonic effusions?
Pleural fluid pH is NORMally around 7.64. Therefore a pH < 7.3 indicates pleural inflammation and a pH < 7.2 indicates need for chest tube aspiration to prevent aspiration. Values that do NOT fall below that threshold can be considered transudative effusions.

Note: pleural fluid to serum fluid protein and LDH ratios are also helpful.
Suspect what if a middle-aged adult complains of superficial unilateral hip pain that is exacerbated by external pressure to the upper lateral thigh (as when lying on the affected side in bed) OR with external rotation OR resisted abduction?
trochanteric bursitis - inflammation of the bursa surrounding the insertion of the gluteus medius onto the femur's greater trochanter.
difference btn Mobitz type I or Mobitz type II heart block?
type I - progressive beat-to-beat increase in PR interval until a ventricular beat is dropped, then the sequence is repeated. A benign arrhythmia and is transient.

Type II - a NORMAL PR interval followed by a SUDDEN dropped QRS complex.
Drooping of the contralateral pelvis that occurs when the patient stands on one foot is called the __________ sign.
Trendelenburg - Normally the gluteus medius and gluteus minimus muscles, which are both innervated by the superior gluteal nerve function to counteract this. Weakness of these muscles in neuromuscular dz, impingement of or trauma to the SUPERIOR GLUTEAL nerve, or inflammatory myopathies, results in a positive Trendelenburg sign and gait.
treatment for UREMIC pericarditis?
hemodialysis - NSAIDS may worsen renal failure and therefore not the appropriate choice in this type of pericarditis.
Suspect what in a pt who presents with confusion, flank pain, acute renal failure, anion gap metabolic acidosis, and hypOcalcemia?
ethylene glycol poisoning - Treatment involves fomepizole or ethanol to achieve alcohol dehydrogenase inhibition, sodium bicarb to alleviate the severe acidosis and/or hemodialysis in the case of resistant acidosis and/or end organ damage.
Management of a solitary pulmonary nodule in LOW risk patients (<40 years and non-smokers) versus HIGH risk?
low risk - ask for an old XR to look for change in last 12 months. No change is considered benigh. Follow nodule by CXR every 3 months for the next 12 months to look for growth or symptoms.

high risk - full workup - CT scan of the chest to get a better picture of the lesion followed by fine needle aspiration.
Most common malignant tumor of the eyelid?
basal cell carcinoma - most commonly on the lower eyelid margin as a slow-growing papule with pearly, rolled borders and overlying telangiectasia.
Diffuse cortical and subcortical atrophy which is disproportionately greater in the temporal and parietal lobes especially the hippocampi is indicative of?
Alzheimer's dz.

Note: frontotemporal dementia shows marked atrophy of the frontal and temporal lobes.
Differences in Alzheimer's versus frontotemporal dementia?
frontotemporal dementia usually presents earlier than alzheimer's at around 40-60 years (alzheimers almost always presents after 60). Initially, frontotemporal lobe dementia has LESS disorientation and memory loss and MORE personality changes and loss of social restraints. Alzheimer's BEGINS with memory loss symptoms that progress to loss of cognitive abilities, reduced daily activities, later leading to confusion and disorientation.
Pleural fluid with a pH<7.2 or glucose < 60 mg/dL is an indication for?
low pH means fluid needs to be drained. low glucose is indication for tube thoracos
tomy.
What does a peripheral smear with spherocytes with NO central pallor indicate?
Either AIHA (autoimmune hemolytic anemia) or heridtary spherocytosis.

Note: AIHA usually has a NEG family hx and is positive for the Coomb's test. If Coomb's test is negative, perorm a micro-Coomb's test to confirm diagnosis.


Hereditary spherocytosis has a POS family hx, positive osmotic fragility test, and NEG Coomb's test.
Patients on MAOIs like phenelzine should avoid foods with tyramine bc?
potential to cause a hypertensive crisis
DOC for congenital long QT syndrome?
beta-blockers
Mode of inheritence for hypertrophic cardiomyopathy?
autosomal dominant
Distinguishing factors btn orbital versus prespetal cellulitis?
orbital - decr eye movements, decr visual acuity, double vision, proptosis. In addition fever, malaise and systemic symproms are a bit more common with this scenario.

preseptal - eyelid discoloration is much more indicative. Eyelid swelling, tenderness, and erythema are also a bit more common in this scenario.
Management of acute exacerbation of COPD?
ipratropium, albuterol nebulization, and systemic steroids.
Contraindications to breastfeeding?
ACTIVE drug abuse, TB or HIV
Suspect what when a pt presents with a unilateral NECK mass that causes difficulty swallowin and increases in size while drinking fluids? And what is the mechanism responsible for this?
Zenker's diverticulum - develops immediately above the upper esophageal sphincter by herniating posteriorly btn the fibers of cricopharyngeal muscle.

Upper esophageal sphincter dysfunction and esophageal dysmotility are believed to cause this problem. Incoordination btn the two results in herniationof the mucosa via a PULSION mechanism.

Surgical treatment includes excision and frequently cricopharyngeal myotomy.
Cause of Meniere's dz?
abnormal accumulation of endolymph within the inner ear.
What is the dx when a child is verbal and talkative at home but refuses to speak in select settings like school?
selective mutism
What nerve is affected if there is paralysis of the deltoid and teres minor muscles as well as loss of sensation over the lateral upper arm?
axillary nerve
Other than resultant hypOthyroidism, what is another side effect of radioiodine therapy for the treatment of Grave's dz?
exacerbation of ophthalmopathy.
Post operative condition that presents with painful swelling of the parotid gland and is aggravated by chewing?
Acute bacterial parotitis usually caused by S. aureus - can be prevented with adequate fluid hydration and oral hygiene
How does the hemoglobing curve change with CO poisoning?
it causes a LEFT shift and a shape change from sigmoid to ASYMPTOTIC.
Which of the following markers has the most impact on the future management of a breast cancer pt?
a) DNA content by flow cytometry
b) oncogene amplification by FISH
c) p53 gene mutations by gel electrophoresis
d) S-phase fraction by flow cytometry
B - overexpression of the oncogene HER2 - positivity predicts a positive response to TRASTUZUMAB and anthracycline chemotherapy.

Note: The other answers indicate negative prognostic factors but will NOT change the MANAGEMENT of the pt.
Best treatment for acute rejection of a transplant?
IV steroids
Best ACUTE treatment for migraines?
IV antiemetics such as chlorpromazine, prochlorperazine, or metoclopramide
Why does furosemide sometimes lead to ventricular arrhythmias?
Bc it commonly causes electrolyte abnormalities like hypOkalemia and hypOmagnesemia. Furthermore, it potentiates side effects of digoxin.

Therefore first step in mgmt would be to order electrolyte and digoxin levels.
Most common cuase of HIV dysphagia/odynophagia?
candidal esophagitis - try a 1-2 week course of empiric oral fluconazole. If symptoms persist, endoscopy with biopsy should be performed to look for CMV esophagitis or HSV esophagitis.
How to distinguish btn CMV and HSV esophagitis?
CMV
1) focal substernal burning pain with odynophagia
2) LARGE, SHALLOW, superficial ulcers
3) presence of intranuclear and intracytoplasmic inclusions

HSV
MULTIPLE, well circumscribed, and SMALL, DEEP ("volcano like") ulcers
How to distinguish a cerebral hemorrhage from a cerebral infarct on CT?
hemorrhage - HYPERdense area

infarct- hypOdense area

Note: atrial fibrillation with warfarin treatment should make you suspicious for EITHER scenario. Some pts are over anticoagulated (especially if on multiple drugs, some of which slow warfarin metabolism) and at higher risk for bleeding. Others are under anticoagulated and at risk for an embolism.
Management of a pt with DVT that has a hx of intracerebral hemorrage?
placement of IVC filter

Note: mgmt would be the same in others whom anticoagulation is contraindicated (recent surgery, bleeding diathesis, or active bleeding).
What is Mulder sign?
A clicking sound/sensation between the 3rd & 4th toes on the plantar surface when simultaneously palpating this space and squeezing the metatarsal joints. Indicates MORTON NEUROMA - mechanically induced degenerative neruopathy commonly seen in runners. Treatment is conservative with bilat show inserts.
Treatments avaliable for condymomata acuminata?
1) chemical/physical agents - trichloroacetic acid, 5-fluorouracil epinephrine gel, and podophyllin

2) Immune therapy - imiquimod, interferon alpha
3) surgery - cryosurgery, excisional procedures, laser treatment
A long term disease modifying treatment for MS?
Glatiramer acetate - works by modulating T-cell mediated autoimmunity to myelin basic protein
When is the drug argatroban used?
It is a selective and reversible thrombin inhibitor - used mainly to prevent thrombosis in pts with HIT who need anticoagulation
Three phases of Trichinellosis (aka trichinosis) caused by eating undercooked pork?
1) during 1st wk of infection - larvae invade intestinal wall and causes abdominal pain, n/v, and diarrhea.
2) during 2nd wk of infection - larval migration causes a local/systemic hypersensitivity reaction causing splinter hemorrhages, conjunctival/retinal hemorrhages, periorbital edema, and chemosis.
3) Larvae enters skeletal muscle causing muscle pain, tenderness, swelling, and weakness.
Management of CHADS2 score of 0, 1-2, and >2?
0 = tx with aspirin
1-2 = tx with either aspirin or anticoagulation
> 2 = tx with anticoagulation
Treatment for aortic regurg (typically a diastolic decrescendo murmur heard best in the LEFT intercostal space!)?
AFterload reduction! Use Ca ch blockers (such as nifedipine) or ACE inhibitors.

Note: DO NOT use beta-blockers as this slows the heart and extends the time of diastole when REGURG can take place thereby worsening AR.
ALL patients suspected of having Zollinger-Ellison syndrome should have what lab investigation?
FASTING SERUM gastrin levels. if this is non-diagnostic, then perform a secretin stimulation test. NORMAL gastric G cells are inhbited by secretin whereas gastrinOMA cells are stimulated. Secretin stimulation resulting in an increased serum gastrin concentration indicates ZE syndrome.

NOT gastric acid secretion study (this is an older study no longer used).
Treatment for CMV vs. HSV esophagitis?
CMV - gancyclovir
HSV - acyclovir
Modality of choice in diagnosing an AAA?
abdominal ultrasound NOT CT. Has nearly 100% sensitivity and specificity, facilitates measurement of aneurysm size, can show associated thrombus, relatively inexpensive compared to CT/MRI, and does not require contrast.
Acute versus long-term treatment of panic attacks?
acute = benzodiazepines

long-term=SSRIs with benzos tapered off to prevent dependence
Management of young child with a simple seizure plus evidence of fever and otitis media?
Treat fever and discharge home. Febrile seizures are commonly associated with viral illnesses or otitis media and a rapid rise in temperature to above 102.2 (39 C). Routine lab tests (such as lumbar puncture) are usually not indicated unless an infectious source is not identified and meningitis is suspected.
Treatment for specific or simple phobias?
benzodiazepines
Management of dyspepsia?
Two categories:
1) Age > 55 with NEW-onset symptoms OR those who have ALARM symptoms (weight loss, dysphagia, or persistent vomiting) should have an upper endoscopy.

2) Others should either undergo empiric treatment with PPIs or should have Helicobactor pylori serology.
Suspect what in a patient who just underwent CABG that begins having fever and chest pain and shows leukocytosis and mediastinal widening on chest XR?
Mediastinitus - complicates 5% of sternotomies. Like an abscess, treatment requires drainage, debridement and ABX therapy.

Note: A postpericardiotomy syndrome (autoimmune in nature) classically occurs several weeks later whereas this occurs soon after surgery.
Major cause of chronic diarrhea in HIV-infected pts with CD4 counts < 180 cells/mm3?
Cryptosporidium parvum
What is unique about the neuromuscular blocking agent ATRACURIUM?
Not metabolized by liver or kidneys. It degrades spontaneously in the plasma and is also hydrolyzed by serum esterases. Safe in liver or renal dysfunction.

Note: Succinyl choline has an an ultra-short duration of action and should be used with extreme caution in pts with hyperkalemia.

Pancuronium and mivacurium are metabolized by the kidneys.

Rocuronium is cleared by the liver.
Gold standard test for diagnosis of acromegaly?
Measure growth hormone levels following an oral glucose load. Most NORMAL individuals will suppress serum GH levels after administration of glucose but patients with ACROMEGALY are unable to suppress and sometimes paradoxically increase the serum GH levels following an oral glucose load.

Note: IGF-1 levels are a very good SCREENING test for acromegaly but should be followed by the gold standard test is still needed for confirmation of the diagnosis.
An important complication of nephrotic syndrome due to antithrombin III lost in the urine?
renal vein thrombosis - antithrombin II deficiency increases risk of venous AND arterial thrombosis. This can occur with any tyope of nephrotic syndrome but most commonly caused by MEMBRANOUS glomerulonephritis in adults.
How is positive predictive value and negative preditive value related to prevalance?
higher the prevalance, the higher the PPV, the lower the NPV.

the lower the prevalance, the lower the PPV, and the higher the NPV
Contraindications to triptans?
1) familial hemiplegic migraine
2) uncontrolled HTN
3) CAD
4) Prinzmetal angina
5) pregnancy
6) ischemic stroke
7) basilar migraine
What kind of murmurs ALWAYS require workup?
diastolic and continuous bc the probability of an organic cause is high.
Criteria for oxygen therapy in COPD?
PaO2 </= 55

SaO2 </= 88%

erythrocytosis (Hct > 55%)

or evidence of cor pulmonale
Bronchogenic cysts are usually found in the _________ mediastinum?
middle
Thymoma is usually found in the __________ mediastinum?
anterior
effect of pH on calcium?
increased pH causes an increased affinity of serum ALBUMIN to calcium --> albumin-bound calcium INCR, ionized calcium level DECR

Decr levels of ionized calcium can result in manifestations of hypocalcemia since ionized calcium is the only physiologically active form.
Treatment of choice for cellulitis WITH systemic signs and WITHOUT systemic signs?
WITH systemic signs - IV nafcillin or if high prevalence of MRSA in area, can use vanco

WITHOUT systemic signs - ORAL dicloxacillin
Most frequently effected dermatomes in shingles?
T3-L3
Drug of choice for herpes zoster?
Valacyclovir but acyclovir is cheaper and also effective.

Note: EARLY antiviral therapy reduces the duration of rash and associated pain and also thought to reduce the likelihood of developing postherpetic neuralgia.
Seborrheac dermatitis occurs with increased frequency in what 2 diseases?
Parkinson's dz

HIV
Pityriasis rosea is caused by what organism?
human herpesvirus 7 - eruption begins iwth a large lesion known as a herald patch and spreads to a "christmas tree" pattern on the trunk
Cholecystectomy is recommended for those with porcelain gallbladder because?
11-33% eventually develop gallbladder carcinoma. Porcelain gallbladder can develop in some patients with chronic cholecystitis and is thought that calcium salts are deposited intramurally secondary to chronic irritation from gallstones or the natural progression of chronic inflammation.
Management of acute symptomatic hypOnatremia versus chronic hyponatremia?
ACUTE - is a medical emergency requiring a prompt increase in the serum sodium concentration. HypERtonic saline solutions can be used in this scenario.

chronic - requires slow correction bc the cells of the brain have adjusted to the hyponatremic milieu and rapid increases in the serum sodium can cause osmotic demyelination syndrome.
A very common side effect of electroconvulsive therapy?
amnesia - anterograde amnesia tends to resolve rapidly while retrograde amnesia may persist longer.
Interesting note:
Both SLE and chronic steroid use are risk factors for ACCELERATED coronary atherosclerosis.
Causes of EXUDATIVE pleural effusions?
infection (pneumonia and tuberculosis), malignancy, pulmonary embolism, connective tissue disease, and iatrogenic causes.
How long should a patient remain on heparin AND warfarin for bridging purposes?
until INR is in the therapeutic range for two consecutive days, at which point warfarin therapy alone is appropriate.
SLE is often associated with false positive tests for?
RPR and VDRL (tests used for the diagnosis of syphillis). Neither are of any use in diagnosing SLE.

Use anti-Smith antibodies and/or anti-double stranded DNA antibodies to confirm SLE.
Differences btn chlamydial and gonococcal urethritis?
chlamydial - MORE common than gonococcal URETHRITS. It has MUCOpurulent urethral discharge and ABSENT bacteriuria and pyuria on U/A.

Gonococcal - Urethral discharge is PURULENT not mucopurulent, and gram stain ususally DOES REVEAL organism.
Major cause of morbidity and mortality in patients with subarachnoid hemorrhage?
Vasospasm at the base of the brain - signs of ischemia usually appear about 7 days after the SAH. Calcium channel blockers (nimodipine) are used to prevent vasospasm.
What causes a transient loss of vision lasting a few seconds with changes in head position and can be confirmed with ophthalmologic examination?
papilledema - caused by increased intracranial pressure which has its own associated symptoms such as morning headaches or changes in headache intensity with position.
PainLESS jaundice plus CONJUGATED hyperbilirubinemia and markedly elevated ALP should raise concern for?
intraabdominal malignancy obstructing the biliary system such as pancreatic adenocarcinoma.
What does beta blocker overdose look like?
bradycardia, hypotension, WHEEZING, AV block, and potential cardiogenic shock.

Atropine and IV fluids are first line treatment. If symptoms do not reverse, glucagon should be administered.
All children aged 2-24 months with a first UTI should undergo?
a VCUG (voiding cystourethrogram) or RNC (radionuclide cystogram).
Management of the incidental finding of several non-tender, rubbery cervical lymph nodes, each approx 1 cm in diameter?
observation for node growth or the development of symptoms. Nodes > 2.0 cm in diameter or firm and immobile are more concerning for malignancy.
Management of a duodenal hematoma (most commonly occurs in children following blunt abdominal trauma) that presents with epigastric pain and vomiting due to failure to pass gastric secretions past the obstructing hematoma?
Treat conservatively with nasogastric suction and parenteral nutrition. Should resolve spont aneously within 1-2 weeks. Surgery (laparoscopy/laparotomy) can be used to evacuate the hemotoma if initial measures fail.
Dx of a rubbery, firm, mobile and painful mass in a young patient who experiences more tenderness during her menses?
fibrocystic dz - treated with aspiration of the cyst which should yield clear fluid and result in the disappearance of the mass. Afterward, pt is typically observed for 4-6 weeks.
Mode of transmission for hereditary spherocytosis?
autosomal DOMINANT
What do patients with hereditary spherocytosis usually begin experiencing by the 3rd decade of life?
Cholelithiasis and/or cholecystitis. Chronic leg ulcers may also be prevalant.
3 common complications of hereditary spherocytosis?
1) Episodes of aplastic crisis in which erythropoiesis is suppressed but the hemolytic process continues.
2) Sometimes intake of folic acid is too low to meet the demands of increased erythropoiesis; therefore all patients should be prescribed folic acid supplementation.
3) If patient has undergone splenectomy, risk is higher for encapsulated organisms so make sure vaccinations are up to date.
What does a shortened PR interval, delta waves, and widening of the QRS complexes signify?
Wolff-Parkinson-White syndrome - an accessory pathway btn the atrium and ventricle
Treatment of choice for an adjustment disorder?
psychodynamic psychotherapy or brief cognitive psychotherapy.
How do patterns of sleep change as people age?
As people age, they tend to sleep less at night and nap during the day. The period of deep sleep (stage 4 sleep) becomes shorter and eventually disappears.
What does a rapidly progressive dementia, myoclonus and an EEG showing sharp, triphasic, synchronous discharges indicate?
Creutzfeldt-Jakob disease - a spongiform encephalopathy caused by a prion. Most pts die within one year of symptom onset.
What is Osgood-Schlatter disease?
A traction apophysitis of the tibial tubercle. During early adolescence, there are periods of rapid growth in which the quadriceps tendon puts traction on the apophysis of the tibial tubrecle (same place where the patellar tendon inserts). This problem is worsened by sports that involve repetitive running, jumping, or kneeling. PE will show edema and tenderness over the tibial tubercle +/- a firm mass (due to heterotropic bone formation). Pain can be reproduced by EXTENDING the knee AGAINST resistance.
Treatment for Osgood Schlatter dz?
activity restriction, stretching exercises, and NSAIDs.
What kind of cancer does SPF protect against?
NON-melanoma skin cancers such as squamous cell carcinoma.
What is the best means of prevention for malignant melanoma?
use of protective clothing! Currently data shows little to no protection against melanoma with the use of sunscreen lotions with SPF 15-30; however, these can protect from non-melanoma skin cancers.
Most common side effects of digoxin toxicity?
GI - anorexia, nausea, vomiting, etc
How should all patients with smoke inhalation be treated?
With 100% oxygen via a non-rebreather facemask due to suspected acute CO poisoning. This competitively removes the binding of CO to hemoglobin and decreases the half life of CO from nearly 5 hours on room air to 1-2 hours.
Appropriate treatment of an anion gap metabolic acidosis following a grand mal (tonic-clonic) seizure?
Most likely due to a postictal lactic acidosis which will resolve within 60-90 minutes following resolution of seizure activity. Therefore observe and repeat labs after 2 hours.
Different types of transfusion reactions?
1) ABO mismatching - an acute HEMOLYTIC transfusion reaction that develops with an HOUR after the transfusion is tarted. Presents with fever, chills, flank pain, and hemoblobinuria and can lead to DIC, renal failure, and shock.

2) febrile NONhemolytic reactions - most common transfusion reaction. Caused by a reaction to CYTOKINES released by stored leukocytes in the transfused blood products. Causes fevers, chills, malaise. The reaction can be prevented by using leukoreduced blood, particularly if the RBCs are washed.

3) IgA deficiency- a major risk for ANAPHYLACTIC reaction to blood products taking place SECONDS to MINUTES of the infusion. Can be prevented by using IgA deficient blood products or performing extra washes of blood product.

4) Despite screening, a very small percentage of blood products are contaminated with infectious organisms. Pts may develop fever within 24 hours.

5) Delayed hemolytic transfusion - results from an anamnestic antibody response to an RBC antigen to which the pt has previously encountered (through exposure in pregnancy, transplant, or transfusion). The antibody is undetectable prior to transfusion but REAPPEARS rapidly following transfusion. It typically causes low-grade hemolysis 2-10 days after the transfusion.
What happens to cardiac index, total peripheral resistance, and left ventricular end-diastolic volume in systolic heart failure?
CI decreases

TPR increases 2dry to neurohumoral activation from SANS activation and the RAAS pathway.

LVEDV increases
Treatment for clavicle fracture in an infant?
no treatment - advise pt to avoid applying tension to the arm. Fracture heals wi 3-6 weeks.
Treatment for lithium induced diabetes insipidus?
This is a nephrogenic DI caused by lithum accumulation in the kidneys that directly damages the renal tubules. In such cases, AMILORIDE is the preferred agent bc it prevents further lithium accumulation in the renal tubules. If CNS dysfunction and significant dehydration, IV normal saline is also recommended.
Gold standard for diagnosing avascular (aseptic) necrosis?
MRI!!! Scintography can also be used. Radiographs are NORMAL!
Well known causes of avascular (aseptic) necrosis?
chronic corticosteroid therapy, alcoholism, and hemoglobinopathies.
Best initial choice of antibiotics in IV drug abuse related endocarditis?
Vancomycin
Indicators of a SEVERE asthma atack?
normal to increased PCO2
speech difficulty
diaphoresis
altered sensorium
cyanosis
"silent" lungs

Note: In an asthma attack, hyperventilation is usually present due to the increased work of breathing. Therefore PCO2 should be DECR. Normal to incr levels indicate CO2 retention bc of severe airway obstruction (air trapping) or respiratory fatigue.
What is the most important drug target in a pt showing an abnormal chromosome 22?
Abnormal chromosome 22 is the Philadelphia chromosome - formed by the reciprocal translocation of chromosomes 9 & 22 resulting in the BCR-ABL fusion gene which leads to abnormal tyrosine kinsase activity. (This is found in CML). Treatment should be tyrosine kinase inhibitors like imatinib (Gleevac) which binds to the ATP binding site of the BCR-ABL protein, prohibiting the confirmation change to its active form.
All trans retinoic acid is a crucial compnent of therapy for what type of leukemia?
acute promyelocytic leukemia
Keys to management of nephrolithiasis?
1) CT scan of abdomen is study of choice (KUB does not detect radioLUCENT stones).
2) Narcotics and NSAIDS - use NSAIDS in normal renal function bc narcotics can exacerbate nausea/vomiting.
3) Stones smaller than 5 mm will pass spontaneously. Increase fluids to greater than 2L daily.
Normal bell shaped distribution?
68% within 1 std deviation

95% within 2 std deviations

99.7 within 3 std deviations
Another name for erythema multiforme major (characterized by sudden onset target-shaped MUCOcutaneous lesions and SYSTEMIC signs of toxicity?
Stevens Johnson syndrome - involves an immune COMPLES mediated hypersensitivity. Most commonly associated with sulfonamides, NSAIDs, and phenytoin. Tx is similar to that of burns - primarily supportive with regular assessment of hemodynamic stability, fluid status, and pain control.

Note: Erythema multiforme minor is similar but usually occurs after a herpes simplex infection, mucosal involvement is rare, and systemic symptoms are less severe.
How long should bereavement last?
A normal grief reaction typically subsides by 6 months after the initial loss and the bereaved individual begins to move forward with their usual daily activities. However symptoms can recur for up to 1 year, especially on particular days such as anniversaries.

Note: Pts who have at least 2 weeks of symptoms of depression 6-8 weeks after a major loss should be considered for BOTH psychotherapy and a trial of antidepressants.
Benefits of note in the use of Bupropion as an antidepressant?
Particularly noted for improving the impaired CONCENTRATION and diminished ENERGY that many depressed patients experience. Does NOT cause SEXUAL dysfunction.
Definition of microalbuminuria?
urine albumin excretion btn 30-300 mg/24 hr (normal urine protein excretion is <30 mg/24 hour).
Good screening method for microalbuminuria?
spot urine collection and timed urine collection for the measurement of urine microalbumin to creatinine ratio.

Note: 24-hour urine collection is slightly more accurate in screening for microalbuminuria but is inconvenient for patients, making it less preferred by physicians.
Manifestations of steroid myopathy, both acute and chronic?
acute - UNcommon - diffuse muscle weakness and rhabdomyolysis during high-dose steroid treatment

chronic - more COMMON - insiduous onset of PROXIMAL muscle weakness withOUT significant pain.

Note: Both conditions improve with discontinuation of steroids.

Note: ESR is NORMAL.
"Risk" is a measure of ________ of a disease.
incidence
Important points to remember about phosphodiesterase inhibitor treatment?
1) Sildenafil is CONTRAINDICATED in patients being treated with NITRATES, and in those who are hyper sensitive to sildenafil.
2) Use with precaution in conditions predisposing to priapism.
3) Concurrent use of drugs which interfere with the metabolism of sildenafil (e.g. erythromycin, cimetidine) may predispose to adverse reactions by prolonging its plasma half-life.
4) While combining with an ALPHA-blocker, it is important to give the drugs at least a 4-hour interval to reduce the risk of hypOtension.
Suspect what in a pt recovering from an URI with sudden worsening of symptoms such as copious amounts of yellowist blood-streaked sputum, temperature of 104, and CXR infiltrates bilaterally as well as multiple, midfield thin-walled cavities?
Secondary bacterial pneumonia (especially common in elderly patients) - this in particular is an acute necrotizing pneumonia with secondary pneumatoceles, i.e. S. aureus causing multiple nodular infiltrates that cavitate to cause small abscesses.
Hodgkin's disease is a curable lymphoma that tends to affect young patients but can, unfortunately, lead to _________ malignancies.
Secondary - highest when chemo is combined with radiation. Up to 3.2% will develop a 2dry malignancy within 20 years of treatment. Lung and breast cancers are among the most common.
Rapidly developing hyperandrogenism with virilization is highly suggestive of?
An androgen-secreting neoplasm of the ovary or adrenal gland. Serum testosterone and DHEAS levels can help differentiate.

ELEV testosterone & NML DHEAS=ovarian source

NML testosterone & ELEV DHEAS=adrenal source
Suspect what with severe pain radiating to the back with difficulty walking due to leg weakness?
aortic dissection - once dissection progresses to include the DESCending aorta, possibly with ischemia of the arteries feeding the spinal cord, it can lead to leg weakness.
Defective bone mineralization is due to?
osteomalacia or Vit D deficiency
Defective mineralization of BOTH bone AND cartilage is due to?
Rickets
Acute pain and swelling of the midline sacrococcygeal skin and subcutaneous tissues are most commonly due to?
pilonidal disease - most prevalant in young males, particularly those with larger amounts of body hair. Believed to develop following chronic activity involving sweating and friction of the skin overlying the coccyx within the superior gluteal cleft. INfection of hair follicles in this region may spread subcutaneously forming an abscess that then ruptures forming a pilonidal sinus tract. This chronic sinus tract may then collect hair and debris resulting in recurrent infections and foreign body reactions. Treatment is by drainage of abscesses and exision of sinus tracts.
Treatment for type A vs Type B aortic dissections?
Type A - involve the ASCENDING aorta - treat with medical AND surgical therapy.

Type B - involves only the descending aorta - treat with medical therapy alone.

Note: Medical therapy in both types involves beta-blockers (such as labetalol) bc it simultaneously lowers heart rate AND BP.
Recurrent hemarthroses in patients with coagulopathies lead to a joint injury called:
hemophilic arthropathy - characterized by iron (hemosiderin) deposition and synovial thickening with fibrosis.
Differential diagnosis for an ANTERIOR mediastinal mass?
the "4 Ts"
1) thymoma
2) teratoma (and other germ cell tumors)
3) thyroid neoplasm
4) terrible lymphoma
how to distinguish btn seminomas and nonseminomatous (mixed) germ cell tumors?
seminomas - b-hCG is high

nonseminomas - AFP is high and often b-hCG is ALSO high.
Know renal diagnosis based on casts! high yield.
Muddy brown casts?
RBC casts?
WBC casts?
Fatty casts?
Broad/waxy casts?
Muddy brown cast = ATN
RBC casts = glomerulonephritis
WBC casts = interstitial nephritis (eosinophilic casts more specifically) and pyelonephritis
Fatty casts = nephrotic syndrome
Broad/waxy casts = chronic renal failure
What vaccine is known for eliciting a T-cell INDEPENDENT B-cell response?
the adult 23-valent pneumococcal vaccine which contains capsular POLYSACCHARIDES.
What kind of vaccines elicit a T-cell-DEPENDENT B-cell response?
the heptavalent pneumococcal vaccine approved for use in children only - it is conjugated with PROTEIN which induces a T-cell DEPENDENT response. Also many vaccines coupled with bacterial TOXOIDS work in the same way, eg. tetanus toxin.
What is well known vaccine that promotes an IgA response?
oral polio vaccine - promotes the development of anit-poliovirus IgA antibodies in the GI tract.
Manifestation of impetigo?
presents as an itchy, erythematous macule which rapidly evolves into vesicles and pustules that rupture to leave honey-colored, crusted exudates. There are 2 forms:

vesiculo-pustular = streptococcus

bullous = staphylococcus
A defect or deficiency in C1 inhibitor leads to elevated levels of the edema-producing factors _________ and __________.
C2b and bradykinin
The most common cause of small bowel obstruction?
adhesions, usually from abdominal operations or inflammatory processes.
Gold standard for diagnosis of avascular necrosis of the hip?
MRI
The presence of bilirubin in urine is indicative of?
a conjugated hyperbilirubinemia
Class IC antiarrhythmic medications elongate the period of depolarization resulting in a prolongation of the action potential by what mechanism?
blocking sodium channels - this results in slowed conduction through the AV node and HIs-Purkinje system.

Note: Of class I agents, class IC meds have the SLOWEST binding and dissociation from the sodium channel giving it the property of use-dependence, i.e. it is more effective at higher heart rates bc there is not much time btn heartbeats for the medication to dissociate from its receptor.
What is the "use-dependence" phenomena of antiarrhythmics?
certain antiarrhythmics are more effective at higher heart rates bc there is not much time btn heartbeats for the medication to dissociate from its receptor. This is particularly seen with class IC meds such as flecainide and class IV meds. Class I meds prolong QRS whereas class IV meds do not.
A non stress test is considered reactive if...?
2 or more heart rate accelerations of 15 bpm above the baseline that last for 15 seconds over 20 minutes of observation.
Dx for rapidly progressive skin lesions that develop into nontender nodules with central necrosis in immunoCOMPROMISED patients?
ecthyma gangrenosum - disorder associated with Pseudomonas aeruginosa.
Syncope associated with prodromal nausea, pallor, and diaphoresis is due to what cause?

Syncope associated with prodromal dizziness and blurred vision is due to what cause?
vasovagal syncope

orthostatic hypotension
Temporal-based seizures (as in herpes encephalitis) may present with?
seizures, anosmia, gustatory hallucinations, and bizarre or psychotic behavior.
Dx if TLC is decreased, FVC is decreased, FEV1 is decreased, and FEV1/FVC ratio is NORMAL?
Restrictive lung dz such as pulmonary fibrosis. Bibasalar, FINE, DRY crackles are typically heard.
Difference btn protraction of labor and arrest disorders?
protraction - SLOW progression of cervical dilation. Can be categorized into 3 causes: "power, passenger, or pelvis." I.e. uterine contractions are inadequate, the fetus is too large, or the pelivs is too small. Best next step is an amniotomy to help labor along. If this fails, an intrauterine pressure monitor and oxytocin may be used.

arrest disorder - cervix ceases to dilate after reaching at least 4 cm.
How to distinguish a tuberculous effusion from other types of exudative pleural effusions?
A very high total protein concentration of the pleural fluid, typically greater than 4 g/dL. Also fluid is consistent with a lymphocytic leukocytosis and a glucose level that is MILDLY below serum glucose levels.

Note: empyema shows a predominance of PMN leukocytes and a VERY LOW glucose level in the pleural fluid.
Patients who are newly diagnosed with HIV should receive ____________ soon after diagnosis is made when the CD4 count is high enoubh to mount an appropriate antibody response?
pneumococcal vaccine

Note: prophylactic antibiotics are usually not indicated until the CD4 count is below 200/microliter.

Note: Antiretrovirals are recommended when CD4 count is less than 350/microliter.
primary therapy in malignancy related SVC syndrome?
radiation therapy, although this tx is primarily palliative.
Conditions that predispose patients to the development of aspiration pneumonia?
impaired consciousness (such as alcoholics, epileptics, or patients with a recent stroke), the presence of tracheal or nasogastric tubes, and an impaired gag reflex.
Dx in patients with bullae or urticarial plaques in the FLEXural areas?
Bullous pemphigoid - an autoimmune blistering dz. Pruritis is a very common symptom. Dz is usually not life threatening, but pts require long-term therapy with topical or systemic corticosteroids. Biopsy will show a SUBepdermal blister under light microscopy.

Note: pemphigus vulgaris shows an INTRAepidermal blister.
pharmacologic intervention for overflow incontinence (as in diabetes due to detrusor UNDERactivity) vs. for urge incontinence due to detrusor instability?
overflow incontinence - cholinergic AGonists such as bethanechol.

urge incontinence - muscarinic antagonists
DOC for reducing the risk of esophageal variceal hemorrhage?
non-selective beta-blockers such as propranolol or nadolol.

Note: nitrates, endoscopic band ligation, and TIPS are other options if beta-blockers alone are ineffective.
DOC for primary hyperaldosteronism (Conn's syndrome)?
spironolactone, an aldosterone blocking agent.

Note: Conn's is due to bilateral adrenal HYPERPLASIA whereas hyperaldosteronism can also be caused by a functioning adrenal adenoma which would require surgical resection, not pharmacological management.
Dx in a pt with elevated Ph, low Ca, along with renal dysfunction and bone pain?
renal osteodystrophy - where chronic renal failure leads to a REDUCED GFR which leads to phosphate retention AND abnormal processing of Vit D by the kidneys resulting in hypOcalcemia.

Both of these abnormalities serve to stimulate the parathyrod gland, leading to parathyroid hypertrophy and 2ndry hyperparathyroidism.