USMLE secrets Flashcards

(34 cards)

1
Q

digitalis moa, tox, treatment?

A

tox: diarrhea, vomiting, increased PR interval, arrythmias, blurry yellow vision (cholinergic effects); stop dig, give potassium/mg/Fab fragments; lidocaine for arrhythmia

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2
Q

things causing eosinophilia?

A

helminths, asthma, allergic disorders, AIN, hodgkins lymphoma

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3
Q

drugs ass with AIN?

A

penicillins, cephalosporins, sulfonamides, NSAIDs, PPIs

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4
Q

ADPKD vs ARPKD

A

ARPKD presents in infancy and is always associated with liver abnormalities: hepatic cysts, congenital hepatic fibrosis/organ dysfunction

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5
Q

VHL

A

bilateral kidney cysts, AD, mutiple types of neoplasms and hamartomas; hemangioblastomas of CNS and retina, pheos, pancreatic tumors, renal cysts predispose to RCC

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6
Q

tuberous sclerosis

A

AD, multiple cysts and tumors in kidney with CNS tuber formation + skin lesions, subungual/periungual fibromas, astrocytoms, renal angiolipomas, retinal hamartomas, cardiac rhabdomyomas

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7
Q

drugs that case oto and nephrotoxicity

A

loop diuretics, vancomycin, cisplatin, aminoglycosides

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8
Q

struvite vs uric vs cystine stones ppt at high/low pH?

A

struvite ppt at High pH; uric ppt at low PH; cystine at low pH

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9
Q

which stones can be seen on xray?

A

calcium stones; cystine/uric acid stones are organic and cannot be seen on x-ray

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10
Q

stones in Crohn’s

A

gall stones and kidney stones–calcium oxalate

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11
Q

CYP450 inhibitors

A

cimetidine, macrolides, azoles, isoniazid, sulfonamides, grapefruit juice, protease inhibitors, ciprofloxacin

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12
Q

CYP450 inducers

A

barbiturates, quinidine, rifampin, phenytoin, griseofulvin, carbamazepine, st john’s wort, chronic alcohol use

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13
Q

treatment for Gilbert or Crigler najjar Type 2?

A

phenobarbital–increases UDP glucoronyltransferase activity

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14
Q

treatment for Dubin johnsons?

A

avoid estrogens

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15
Q

treatment for crigler najjar type 1?

A

phototherapy bridge to liver transplant

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16
Q

treatment for rotor syndrome?

17
Q

diseases that hepB makes you susceptible to?

A

liver disease/HCC; glomerulonephritis (Ab-Ag deposition in glomerulus); polyarteritis nodosa; HepD infection

18
Q

HCC mets to where?

A

lungs, adrenals, regional lymph nodes

19
Q

HCC paraneoplastic syndromes?

A

IGF-1–>constitutional hypoglycemia; EPO; PTHrP

20
Q

substances that signal through cAMP

A

FLAT P + HCG: FSH, LH, ACTH, TSH, PTH, hCG, CRH, glucagon

21
Q

substances that signal through cGMP

A

NO, ANP (vasodilators)

22
Q

substances that signal through IP3 (Gq)

A

GnRH, GHRH, oxytocin, TRH

23
Q

substances that signal through steroid receptors

A

Estrogen, testosterone, glucocorticoids, vitD, aldosteron, progesterone, T3/T4

24
Q

substances that signal through tyrosine kinases

A

insulin, growth factors, GH, prolactin

25
tuberoinfundibular stalk disruption by head trauma?
all anterior pituitary hormones decreased because lose hypothalamic stimulus, except prolactin which increases because dopamine (via hypothalamus) is no longer inhibiting prolactin
26
licorice inhibits...and can cause?
inhibits 11B-HSD, enzyme converts cortisol--cortisone-->hypertension and pseudohyperaldosteronism-->metabolic alkalosis
27
POMC cleavage gives...which hormones?
ACTH and MSH in the anterior pituitary
28
neisseria meningitis-->adrenal?
Waterhouse Freidrichson: adrenal hemorrhage, septicemia, DIC, petechial rash
29
neural crest derived cells:
chromaffin cells, parafollicular thyroid cells, Schwann cells, ANS, dorsal root and celiac ganglia, melanocytes, cranial nerves, pia/arachnoid, odontoblasts, skull bones, aorticopulmonary system
30
neural crest derived tumors?
pheo and neuroblastoma, medullary thyroid (parafollicular)
31
methimazole vs PTU
both inhibit thyroperoxidase (organification) centrally, only PTU inhibits T4 to T3 conversion peripherally via inhibtion of 5-hydroiodoinase (something like that)
32
meds that can cause hypothyroidism
amiodarone and lithium
33
drugs that induce uterine contractions
alkaloids (ergonovine), triptans, synthetic prostaglandins
34
X-linked immunodeficiencies?
Missing WBCS: hyper IgM syndrome, Wiscott-Aldrich syndrome, Bruton's aggama..; chronic granulamatous disease, SCID;