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193 Cards in this Set

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HIV, low CD4 count with multiple, discrete, red-colored papules of varying size and slight central umblications.

Cutaneous Cryptococcous; cryptococcus neoformans (fungi) --> early sign of disseminated infection check CXR, blood and CSF Cx

small, sharply marginated, reddish brown papillose with gelatinous consistency (apple-jelly) lesions with central atrophy

MC form of cutaneous tuberculosis (lupus vulgaris)

How to diagnose Cutaneous Cryptococcosis

Biopsy, histology: graulomatous inflam run with multinucleated giant cells, histiocytes, lymphocytes, neutrophils, and plasma cells with numerous yeast-like organisms




stains like PAS (periodic acid schiff) and Gomori's meth silver nitrate help identify

Stain for CSF with suspected Cryptococcosis

India Ink

Low RAIU (radioactive iodine uptake) vs Increased RAIU

thyroditis =low


graves synd (increased thyroid synthesis dzs) and toxic adenoma=increased

Postpartum thyroiditis


- presentation?


- RAIU?


-anything else?


-painful vs painless?

initially results in hyperthyroidism followed by hypothyroidism, has a low RAIU, is painless, and may have positive anti-TPO antibodies

Thyroid issue with Pain in thyroid

Subacute granulomatous thyroiditis (DeQuervain's)

Iritis

Aka Anterior Uveitis




pain, redness, variable visual loss and constricted and irregular pupil




visualization of leukocytes in anterior segment confirms diagnosis

leukocytes in anterior segment of eye

Iritis aka anterior uveitis

increased PTH and hypercalcemia




-urinary ca >200mg/day = ?


-urinary ca <100 mg/day= ?

-urinary ca >200mg/day = primary hyperparathyroidism


-urinary ca <100 mg/day= familial hypocalcuric hypercalcemia

actinic keratosis


-cause?


-look?


-associated with?

- cause: sunlight


- look: unexposed areas, small, rough, erythematous and keratotic papules


-associated with squamous cell carcinoma (SCC)

HIV; what are CD4 count indicator of? what is viral load indicator of?

CD4: indicator of current level of immunosuppression, "the immunologic damage that has already occurred"




Viral load: good marker of disease activity or potential for future damage, "the damage that is about to occur"

exposed to TB, PPD today negative, what to do next?

repeat PPD 3 months

Two step approach for screening and diagnosing GDM

-At 24-28 weeks GA


- Step 1: 50g oral glucose check 1 hr later --> if <140 fine, no more tx; equal to or >140 then move to Step 2


-Step 2: 100g oral glucose load, check fasting serum glucose & each hr until 3 hrs --> dx with 2 abnormal values: fasting >95, 1h >180, 2 hr >155, 3 hr >140



Treatment in GDM decreases risk for what for baby?

- reduce risk of fetal macrosomia and shoulder dystocia




-do NOT reduce the risk of neonatal metabolic outcomes such as hypoglycemia

If mom hx of HSV, when start antiviral therapy?

36 weeks GA

case fatality ratio definition

proportion of people with a particular condition who end up dying from the condition

Mortality rate definition

general population's likelihood of dying from the disease

treatment for SBP

fluoroquinolone (ofloxacin, norfloxacin or ciprofloxacin) for 7-10 days

patients with recent variceal bleeding, complications that lead to increased mortality are:

-infections, hepatic encephalopathy, and renal failure


-MC complication is infection: UTI, SBP, respiratory infection, aspiration PNA, or primary bacteremia

HUS associated with which infection

E coli 0157:H7; shiga toxin

DKA treatment: serum glucose <200 but still elevated anion gap, do what?

rate of infusion should be halved and dextrose (D5) added to the IV fluids to prevent hypoglycemia

Anion Gap calculation


?normal

Serum Na- (serum Cl + Serum K)


normal value: 7-13

when to add K to treatment when DKA treatment

add IV fluids if serum K levels are <5.2

Corrected Serum Sodium with DKA/high glucose and what values mean what

*measured sodium + 0.016 (measured glucose-100)


* if corrected Na <135, continue NS


* if corrected Na >or = 135, change to half NS 0.45%

When to start SQ insulin vs IV during DKA

*switch to SQ insulin for the following: able to eat, glucose <200, anion gap <12, serum Hco3 >15


*overlap SQ and IV insulin by 1-2

When to consider bicarb for DKA

When pH <6.9

When to give K for DKA

*add IV K if serum K <5.2


*hold insulin for serum K <3.3



Dx of pheochromocytoma

*plasma free metanephrine


OR


*24-hour urine collection for measurement of catecholamine and metanephrine

Tx of pheochromocytoma in attack

alpha-adrenergic 1st then beta; if do beta first can worsen HTN bc unopposed alpha would cause vasoconstriction

Reasons to test for pheochromocytoma

*family hx of pheochromocytoma


*episodic headaches, diaphoresis or tachycardia


*early-age onset of HTN


*refractory HTN


*familial syndromes (eg MEN2, NF-1, von Hippel-Lindau)


*adrenal mass discovered incidentally on imaging


*idiopathic dilated cardiomyopathy


*paroxysmal HTN and/or tachycardia during common procedures

Next step if Dx with pheochromocytoma

MRI or CT of abdomen


*+ then sx eval, genetic testing, alpha and beta blockade prior to sx, MIBG scan if tumor >5cm and suspicion of extra adrenal disease


*- then consider further imaging: MIBG scan, octreotide scan, whole body MRI, PET scan

Tx for Tourettes

antipsychotics like risperidone

Dx for Rocky Mountain Spotted Fever

-treat empirically don't wait for confirmation of diagnosis


- delayed tx associated with increased mortality

Tx for Rocky Mountain Spotted Fever

Doxycycline


-if pregnant, then chloramphenicol

RMSF rash

petechial rash begins on ankles and wrists, and spreads to palms and soles and to the central body

initial diagnostic test for polycythemia

EPO


-low: suggests polycythemia vera


-high: suggests secondary cause of polycythemia vera like chronic hypoxia or a hormone producing neoplasm (commonly RCC)

most common association complication from compartment syndrome

acute renal failure due to rhabdomyolysis in limb causing myoglobin release and damage kidney leading to ARF (esp if volume depleted)

Compartment syndrome diagnosis

measurement of tissue pressures: >30 mm Hg or delta pressure (diastolic BP-compartment pressure) <20-30mmm Hg

Male puberty delay

*dx if he does not have testicular enlargement by 14 yoa, or if testicles are 2.5 cm or less in diameter


*another criteria: delay of development for 5 or more years from onset of genitalia enlargement

MCC of delayed puberty

constitutional delay

Delayed puberty initial testing

*bone age XR L wrist


*if bone ages older or equal to age then need to rule out chromosomal abnormality and endocrine causes


* growth chart


*tanner staging

Dx test for esophageal perforation

esophagogram with water-soluble contrast


-CT ok but would miss small tears


-NEVER GI endoscopy

hypocalcemia symptoms

perioral numbness, muscle cramps, carpopedal spasm, + Chvostek sign (same side contraction of facial mm on tapping angle of jaw) and + Trousseau's sign




severe: mental status changes and seizures

Lab findings in SIADH

hyonatremia, decreased plasma or serum osmolality, increased urine osmolality (bc excessive fluid retention), urinary sodium concentration of >40 mEq/L and normal renal, adrenal and thyroid functions

MAOIs

Monoamine oxidase inhibitors


-phenelzine, tranylcypromine

SSRI

selective serotonin reuptake inhibitors


-fluoxetine, paroxetine, sertraline, citalopram

Serotonin syndrome symptoms

mental status change, autonomic dysregulation (diaphoresis, tachycardia, HTN, hyperthermia, D, mydriasis) and neuromusclar hyperactivity (eg hyperreflexia, tremor, rigidity, myoclonus, ocular clonus)

Anticholinergic toxicity symptoms

dry skin, flushing, fever, mydriasis, altered mental status

Neuroleptic malignant syndrome

a rare idiosyncratic reaction to dopamine antagonists; like serotonin syndrome but no hyperreflexia or clonus. also has "lead pipe" muscular rigidity

Mono workup dx

1st monospot


-if + stop Dx


-if - then EBV specific AB (+IgM and +IgG viral capsid antigen= acute infection; if +IgG EBV nuclear Ag then NOT acute it is chronic/past, only appears 6-12 weeks after onset)

recumbent position

lying down

Only treatment for Mono and when

if patient develops severe complications (eg airway obstruction, overwhelming infection, aplastic anemia, thrombocytopenis) then tx with corticosteriods (IV)

Pressure ulcer stages

1- nonblanchable erythema of intact skin


2- superficial ulcers causing a partial thickness loss of epidermis, dermis or both


3- deeper ulcers causing a full thickness loss with damage to subcutaneous tissue that may extend to, but not through, underlying fascia


4- very deep ulcers causing full thickness loss and extensive tissue destruction of mm, bone or structures



Symptoms of femoral nerve lesion

anterior and anteromedial thigh paresthesia with quad mm weakness and decreased knee jerk reflex

Symptoms of L5 and S1 Radiculopathies

back pain that radiates down the lateral or posterior aspect of the leg. Also weakness of corresponding segments also noted

Symptoms of obturator nerve lesion

sensory loss over medial thigh and weakness in leg adduction

symptoms of Meralgia paresthetica

-entrapment of lateral femoral cutaneous nerve


-decreased sensation over anterolateral thigh without any muscle weakness or DTR abnormalities

Clinical features of Tuberculosis

-recurrent PNA (upper lobe/apical)


-recent immigrant


-institutionalized patient


-homeless/lower SES

Clinical features of Post-obstructive cause of recurrent PNA

-cause is polymicrobial


-hemoptysis


-weight loss/cachexia


-PNA in same location

Clinical features of Recurrent PNA due to aspiration

- pt has hx of seizures, dysphagia, alchohol intoxication


- causes anaerobes, polymicrobial


- R middle lobe/lower lobe PNA


- Dysphagia/dysarthria


- Altered mentation

CSF findings normal

WBC 0-5


Glucose 40-70


Protein <40



CSF findings in bacterial meningitis

WBC >1000


glucose <40


protein >250

CSF findings in tuberculosis meningitis

WBC: 5-1000


Glucose: <10


Protein: >250

CSF findings in Viral meningitis

WBC 100-1000


Glucose 40-70


Protein <100

CSF findings in Guillain-Barre

WBC 0-5


Glucose 40-70


Protein 45-1000

Cryptococcal Meningitis CSF findings

elevated opening pressure (>250-300)


lymph predominant with low WBC (<50)


elevated protein and low glucose


+ India Ink prep or cryptococcal Ag test




**be careful of increased ICP if pt also has HA, blurry vision etc

Tx of Cryptococcal Meningitis

-Induction Tx: amphotericin B and flucytosine for 10-14 days


-If clinical improvement then discontinue and start fluconazole for maintenance therapy and prevent recurrence

Cardiac complications of infectious endocarditis

-valvular insufficiency- common cause of death


-Perivalvular abscess


-conduction abnormalities


-mycotic aneurysm

Neuro complications of infectious endocarditis

-embolic stroke


-cerebral hemorrhage


-brain abscess


-acute encephalopathy or meningoencephalitis

Renal complications of infectious endocarditis

-renal infarct


-glomerulonephritis


-drug-induced acute interstitial nephritis from therapy

Musculoskeletal complication of infectious endocarditis

-verterbral osteomyelitis


-septic arthritis


-musculoskeletal abscess

lifestyle interventions to manage acne

-water based skin products (non oil based)


-ph neutral detergent cleansers


-low glycemic index diet


-avoidance of saturated fats, dairy, and refined carbs

Tx tinea capitis


Dx?

-clinical dx, confirmed with KOH prep


-tx: oral griseofulvin and terbinafine

Pernicious anemia

megaloblastic anemia --> atrophic gastritis (autoimmune destruction of gastric parietal cells and inactivation of intrinsic factor) --> lack of IF and vit b12 deficiency




*test for anti-IF antibodies



Pernicious anemia associated with what gastritis

autoimmune metaplastic atrophic gastritis (AMAG): glandular atrophy (of fundus and gastric body), intestinal metaplasia and inflammation

Type I vs Type II error

Type 1 error (alpha): false positive (reject null but it is true)



Type 2 error (beta): false negative (fail to reject null but null is false)



Power=

1- Beta error

Erysipelas caused by

Group A strep

Acute stress disorder vs PTSD

acute stress: 3 days - 1 month after event


PTSD: >1 month after event

lead time bias

when screening test detects the disease at an earlier point in time (making it look like the survival rate increased), but associated prognosis does not change



-let those with the disease known earlier, but doesnt change the diagnosis



hospice vs palliative care

-hospice is a model of palliative care offered to patients at end of life when life-prolonging therapy is NO LONGER INDICATED




-palliative care can be done concurrently with disease-modifying medical therapies

CO poisoning symptoms

throbbing HA, nausea, malaise, and dizziness




-esp if multiple simultaneously present with a HA

mentzer index

ratio of MCV/total RBC




high mentzer >13 = iron deficiency anemia


low mentzer < thalassemia

H pylori treatment

Pantoprazole, clarithromycin and amoxicillin




if allergic to penicillin then substitute metronidazole for amoxicillin

meningococcal ppx for close contacts/dr who intubated

rifampin (4 PO doses)


Ceftriaxone 1 IM, can be used in reg


Ciprofloxacin (PO once; not in children)

Sickle cell anemia lab values and peripheral blood smear findings

low Hct, high reticulocytes, high serum low-density lipoprotein, increased unconjugated bilirubin




-peripheral smear: sickled red cells, howell-jolly bodies

Acute Chest Syndrome, Dx and Tx

*in sick cell


*Dx: new pulmonary infiltrate on CXR PLUS >1 of the following:


-increased work of breathing, cough, tachypnea, wheezing


-temp >38.% C (101.3F)


-hypoxemia


-chest pain


*initial treatment: ceftriaxone+azithromycin


IV fluids and pain control

EKG findings in paroxysmal SVT

narrow and regular QRS complexes and no P waves

EKG findings in sinus tachycardia

P waves, along with narrow QRS complexes

EKG Findings in atrial fibrillation

arrhythmic arrhythmia; rhythm is irregular and P wave is absent

EKG findings in ventricular tachycardia

wide QRS complexes (more than 0.12 sec)

EKG findings in atrial flutter

"flutter waves" in a saw tooth pattern; the HR of 'typical' atrial flutter with 2:1 conduction is usually around 150 bpm

EKG findings in Wolf-Parkinson White Syndrome

slurred upstroke of the initiation of QRS/ventricular activation (called delta wave)




PR interval of <0.12 sec

Uses and Side effects of Ginko biloba

-memory enhancement


-increases bleeding risk

Uses and Side effects of Ginseng

-increased mental performance


-increased bleeding risk

Uses and Side effects of saw palmetto

-BPH (benign prostatic hyperplasia)


-SE: mild (stomach discomfort) and increased bleeding risk

Uses and Side effects of Black cohosh

-post-menopausal symptoms (hot flashes and vaginal dryness)


-SE: hepatic injury and increased bleed risk (anti platelet properties)

Uses and Side effects of St John's wort

-for: depression and insomnia


-SE: drug interactions like antidepressants (serotonin syndrome), OCP, anticoagulants (decreased INR), digoxin

Uses and Side effects of kava

for: anxiety and insomnia


SE: severe liver damage

Uses and Side effects of Licorice

for: stomach ulcers, bronchitis/viral infectionsSE: hypertension and hypokalemia

Uses and Side effects of Echinacea

-for: treatment and prevention of cold and flu


-SE: anaphylaxis (more common in asthma pts)

Uses and Side effects of Ephedra

-for: treatment of cold and flu & weight loss and improved athletic performance


-SE: hypertension, arrhythmia/MI/sudden death, stroke and seizure

VSD physical exam

loud, harsh holosystolic murmur in 4th L intercostal space and a palpable thrill




-large nonrestrictive VSD ass with softer murmur

TOF 4 characteristic anatomical features

right ventricular outflow tract obstruction, overriding aorta, right ventricular hypertrophy, and VSD

Proximal weakness with increased CPK

indicated a muscle disorder




-inflammatory myositis may lead to increased serum ferritin levels (acute phase protein)

Tx inflammatory myositis

high dose glucocorticoids

POEMS syndrome

Polyneuropathy, Organomegaly, Endocrinopathy, M-proteins, and skin changes




-do SPEP to look for M-spike

Pernicious anemia

Vit B12 deficiency (due to lack of intrisic factor secretion in stomach)

when treating pernicious anemia what do u watch for

when starting treatment with vit b12 within the first 48 hours watch serum K level, they are at risk for severe hypokalemia (bc lots of new RBC being made and suck up potassium)

Initial treatment for pulmonary embolism in hemodynamically stable vs non stable patients

stable: anticoagulation with LMWH or heparin


unstable: IV fibrinolytic therapy

what should be ruled out in inital presentation/eval of dementia

hypothyroidismm, vit b12 deficiency, and depression




also check glucose

septum in the uterus associated with?

recurrent pregnancy loss (up to 60%), usually 1st trimester




needs surgical treatment to correct to decrease future miscarriage risks (metroplasty via hysteroscopy TOC)

when to give platelets

<50,000 platelets with life-threatening bleeding

when to give RBC packed

-if have risk of morbidity in setting of severe anemia (eg unstable coronary artery disease) then <9 Hb


-normally <7 Hb

common cause of bacterial infections in contact lens wearers

pseudomonas

mc pathogen isloated from cultures of corneal foreign bodies

coag neg staph (CONS)

RAIU in exogenous hyperthyroidism

low bc thyroid gland is intrinsically making a lower level of thyroid hormone


-thyroglobulin should be low too

what is a unique finding in patients with disseminated gonococcal infection

tenosynovitis (painful tendons along the ankle and toe joints)

most important single risk factor for osteoporosis and osteoporotic bone fracture

age

who is more susceptible to osteoporosis: caucasians or african americans

caucasians

primitive idealization

someone is seen as perfect, part of splitting (defense mech), seen in Borderline personality disorder

reaction formation

person deals with stress by subsituting thoughts, feelings, or behaviors that are the exact opposite of what the person believes, which is considered uncomfortable (example homo man that is homophobic)

most successful way of treating borderline personality disorder

dialectical behavior therapy (behavior modification and building of skills)


-TCA CI due to high suicide AE

Hep B and pregnancy

-screen all preg women for hepB at 1st prenatal visit AND at delivery (if unknown status OR risk factors during preg)


-IF have ACTIVE infection: give hep B vaccine and antiviral therapy to preg woman; then when baby born give both hep B vaccine and HBIG



MC cause of proteinuria in adolescents; how to Dx; and tx

Orthostatic proteinuria; split (day and night) 24 hour urine collection, showing elevated daytime but normal nighttime protein excretion rates


-tx: benign, resolves spont; not a predictor for development of renal abnormal; tx with nothing

fibromyalgia tx

lifestyle: aerobic exercise, sleep hygiene


meds: TCA, SNRI

when should HIV pt be given PCP ppx, and what is it

Trimethoprim/sulfamethoxazole; <200 CD4 count

when should HIV pt be given MAC ppx, and what is it

azithromycin; (mycobacterium avium complex); CD4 <50 (or clarithromycin)

when should HIV pt be given CMV ppx, and what is it

ganciclovir; CD4 <50; THIS ONE NOT WIDELY RECOMMENDED, no increased survival advantage

neonatal chlamydial infections

-Conjunctivitis: age at onset 5-14days, watery, mucopurulent, or blood-stained discharge, TX oral erythromycin 14d


-PNA: age at onset 4-12 weeks; staccato cough, hyperinflation on CXR, tx oral erythromycin 14d

staccato cough

series of short, dry coughs; ass with chlamydial PNA

NNT

number needed to treat:


ARR(absolute risk reduction)=control group event rate-experimental group event rate


NNT= 1/ARR

MC precipitant of Guillian-Barre Syndrome

Campylobacter jejuni (bloody diarrhea)

TX of varicose veins

-1st: leg elevation, weight reduction and compression stockings


- if this failed after 3-6 months, then try injection sclerotherapy w saline, with or without local anesthetics


-those pt with large symptomatic varicose veins with ulcers, bleeding or recurrent thromophlebitis --> surgical ligation and stripping

severe preeclampsia tx

hydralazine or labetalol AND MgSO4 then delivery

MCC of massive lower GI bleeding in elderly pts; ?association

angiodysplasia or diverticulosis




-angiodysplasia associated with aortic stenosis and ESRD

refeeding chronic alcoholic patients at risk for?

hypophosphatemia (in general have low phosphate secondary to decreased Vit D and phosphate intake --> pt body maintains normal levels via extracellular shift normally --> when in hospital and get "refed"/IV hydration it shifts phosphate into the cell and shows the true level

angioedema with ACE inhib (pril)

switch to ARB (Sartan) bc doesnt effect kinin system

solitary, painful, lytic bone lesion with overlying swelling and hypercalcemia

langerhans cell histiocytosis (histiocytosis X or granulomatous)




conservative tx, resolves on own

Adult Still's

inflam disorder with recurrent high fevers (102), rash and arthritis

Rheumatic fever give ? <3 MC

mitral stenosis --> increased risk of atrial fib and cardiac emboli

positive apnea test to confirm brain death

absent respiratory response off the ventilator for 8-10 minutes with PaCO2 >60mmHg (or >20mm from baseline) and a final arterial pH od <7.28

high calcium --> test PTH--> if PTH low ?do next

-measure PTHrP, 25(OH)D and 1,25(OH)D


-*if elevated PTHrP: eval for solid tumor malignancy


*if elevated 1,25(OH)D: CXR for possible lymphoma, sarcoid


*Elevated 25(OH)D: Vitamin D toxicity


*Normal labs: causes hyperthryroidism, multiple myeloma, adrenal tumor, acromegaly, vitamin A toxicity, immobilization, milk-alkali syndrome

1st line tx for nongonococcal urethritis

azithromycin or doxycycline

MC tx of gonorrhea

1 dose Ceftriaxone

when to treat STD G vs Chlamyd

-if have gonorrhea also treat Chlamydia

Throid nodule workup:

*1st do TSH and thyroid US


* if US fine:


-Low TSH: do Iodine-123-scintigraphy


-if hyperfunctional ("hot") nodule: tx hyperthyroidism


-if hypofunctional ("cold") or undetermined nodule: FNA


* If US fine and high or normal TSH: FNA


* if US suspicious: FNA

Colloid goiter

thyroid enlargement in adolescent girls with normal thyroid function and neg anti-TPO

Medullary thyroid cancer typically has elevated ?

calcitonin

Pemberton's sign

presence of facial plethora or neck vein distension when the arms are raised and confirms an enlarged thyroid gland as the cause of esophageal obstructive symptoms

what is a anatomical predisposing factor for Mallory-Weiss syndrome?

Hiatal Hernia

Thompson test

observes plantar flexion when the calf is squeezed; the absence of plantar flexion signifies complete rupture of achilles tendon and +test result

gastrostomy

means putting in a PEG tube (percutaneous gastrostomy)

Charcot's triad

fever, RUQ pain and jaundice --> suggestive of ascending cholangitis

what to give pt wotj HTN and CKD (chronic kidney dz) who has proteinuria?

if excess 500-1000mg/day


-start ACE inhib or ARB

Nipple discharge: pathologic vs physiologic

-Pathologic: unilateral, bloody or serous, lump changes or skin changes and W/U is mamogram +/- US and surgical eval


-Physiological: bilateral, milky/nonbloody, no skin or lump changes, and W/U is Urine HCG and Serum TSH, prolactin

MCC of pathologic nipple discharge

papillary tumor (eg papilloma)

"atypical lymphocytes" on peripheral smear is a clue to?

EBV

dermatitis herpetiformis associated with?

celiac disease

baby born to mom with Hep B; you give Hep B and HIg at birth; when do you test serology?

-2nd Hep B vaccine: 1-2months old; 3rd dose at 6 months


*3-4 months after the 3rd hep B vaccine; so about 9-15 months old

leading cause of mortality in pts with SLE

cardiovascular events; SLE is a significant (50x) risk factor for development of premature coronary atherosclerosis

ALS

-LMN and UMN loss of motor neurons

-weakness associated with progressive wasting, atrophy of muscles, and spontaneous twitching or fasciculation of motor units


-ocular motility, sensory, bowel, bladder and cognitive functions preserved

pyoderma gangrenosum ass with?

inflam bowel disease

explosive onset of muliple itchy seborrheic keratoses ass with?

gastrointestinal malignancy

severe seborrheic dermatitis ass with

HIV infection and parkinson disease

porphyria cutanea tarda and cutaneous leukoclastic vasculitis (palpable purpura) secondary to cryoglobinemia ass with?

hep c

multiple skin tags associated with?

insulin resistance and pregnancy and if perianal, crohn disease

acanthosis nigricans ass with?

insulin resistance and gastrointestinal malignancy

osteonecrosis of femoral head


-ass with?


-staging and treatment

-ass with SLE esp when on high steriods


-Stage 1 or 2: core decompression (+radiographs without femoral head collapse)


-stage 3


-stage 4 (flattening of femoral head and joint space narrowing): total hip replacement

Pruritis in pregnancy:


- physiologic changes of skin:


- pruritis folliculitis:


- pustular psoriasis:


- herpes gestationis:


- PUPPP (papular urticartial papules and plaques of pregnancy):

- physiologic changes of skin: common, no path process, tx with topical steroids, antihistamines, oatmeal baths

- pruritus folliculitis: acne-like lesions


- pustular psoriasis: erythematous plaques with surrounding pustules


- herpes gestationis: urticarial plaques, papules, and vesicles surrounding the umbilicus; tx topical steriods


- PUPPP (papular urticarial papules and plaques of pregnancy): common preg-ass dermatosis, pruritic erythematous papules within striae gravidarum, can spread to extremities, tx topical steriods

inital lab w/u for suspected lead poisoning

CBC, serum iron and ferritin and reticulocyte count

how many weeks of persistent lymphadenopathy before referral?

localized lymphadenolpathy for 3-4 weeks should be referred to sx for biopsy to r/o lymphoma

sensitivity


specificity

-sensitivity (true positivie rate): TP/ (TP+FN) or TP/all sick


-specific (true negative rate): TN/ (TN+FP) or TN/all well

Neg predicitive value


PPV

PPV (precision): TP/ all positive tests


NPV: TN/ all neg tests

MCC of idiopathic nephrotic syndrome in adults (50% of A-A pts)

Focal segmental glomerulosclerosis (FSGS)

age associated causes of secondary hypertension, children and adolescents (birth to age 18)

renal parenchymal disease and coarctation of aorta

age associated causes of secondary hypertension, young adults (age 19-39)

thyroid dysfunction, fibromuscular dysplasia or renal parenchymal disease

age associated causes of secondary hypertension, middle- aged adults (40-64)

aldosteronism, thyroid dysfunction, obstructive sleep apena, cushing syndrome, or pheochromocytoma

age associated causes of secondary hypertension, in older adults ( >65)

atherosclerotic renal artery stenosis or renal failure

signs of seconday hypertension

frequent HA, exertional dyspnea, lower extemity edema, and severe HTN

patient with right varicocele, varicocele that doesnt disappear in supine position, or bilateral vericocele (even if not at same time), what do you need to do

CT scan of abdomen to rule of inferor vena caval obstruction (eg clot, tumor)

vericocele is MC on which side and why

left, bc the left spermatic vein enters the L renal vein at a 90-degree angle

solitary pulmonary nodule on routine CXR, what to do?

*if have previous CXR and stable lesion over 2-3 years, no further testing


*if no previous CXR OR possible nodule growth then do Chest CT


-if ct is benign: serial CT scans


-if CT highly suspicious: surgical excision


-if CT indeterminate or suspicious for malignancy: further investigation with bx or PET



test for organophosphate poisoning and symptoms

-confusion, lethargy, bradycardia, skin flushing, miosis and wheeze with garlic-like odor from clothing

-RBC cholinesterase activity level (confirmation and assess the degree of severity



Dx criteria for multiple myeloma

-monoclonal protein in serum or urine


->10% clonal plasma cells in bone marrow or soft tissue/bone plasmacytoma


-end organ damage (CRAB): Calcium elevated, Renal insufficiency, Anemia (usually normocytic), Bone Pain (usually due to lytic lesions) (or hx of back pain or fracture)

what type of bone imaging should multiple myeloma patients get?

Xray skeletal survery


-if bone pain and negative XRs then can move on to CT, MRI or PET

complications of multiple myeloma

-hypercalcemia (asympt or sympt with N, polyuria, constipation, weakness, confusion), tx with hydration and either dexamethasone (mild) or bisphophonates (mod to severe)


-renal insuff


-infections (highest risk during 1st 3-4 months of therapy


-skeletal bone lesions (bisphophonates for prevention)


-hyperviscosity syndrome


-thrombosis

hyperviscosity syndrome in multiple myleoma

nasal or oral bleeding, blurry vision, neuro symptoms (eg confusion, HA) and heart failure




-plasmapheresis in symptomatic patients


(this syndrome more common in Waldenstrom's macroglobulinemia (elevated IgM))

mucosal hemorrhage a sign of?

eg nasal or oral bleeding


-impaired platelet function

adverse effect of thiazides (hydrochlorothiazide)

photosensitivity rash

bicuspid aortic valve


-etiology


-dx


-complications


-management

-etiology: M>F, 30% of Turner's syndrome, 1% of general pop


-dx: screen echo for patient and 1st degree


-complications: infectious endocarditis, severe regurg or stenosis, aortic root or ascending aortic dilation; dissection


-management: f/u echo every 1-2 years; baloon valvuloplasty or surgery

Cushing syndrome presentation and dx?

Young patients with diabe