Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
193 Cards in this Set
- Front
- Back
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 |