UWorld Test 5/19/2014 Flashcards

1
Q

Cleft lip and cleft palate results from?

A

Failure of fusion of the two lateral maxillary prominences with the interaxillary segment (aka medial nasal prominence) during embroyogenesis. Cleft palate results when the palatine shelve of the maxillary prominence fail to properly fuse with one another or with the primary palate

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2
Q

What is bupoprion, major side effect, toxicity?

A

Increase dopamine and NE with greater effect on dopamine. Toxicity: stimulant effects like tachycardia, insomenia, also headache, SEIZURES IN BULIMIC PATIENTS. Contraindicated in patients with siezure disorder or with current/past history of bulimia/anorexia nervosa

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3
Q

What drugs cause seizures

A

with seizures, I BITE my tongue - INH (vit B6 deficiency), Bupropion, Impinem/cilastatin, Tramadol, Enflurane, Metoclopramide

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4
Q

What is phenoxybenzamine, what is it used for? What is phenolamine

A

Phenoxybenzamine: Irreversible alpha blocker. Give preoperatively to patients with pheochromocytoma to prevent catecholamine (hypertensive) crisis. Toxicity: orthostatic hypotension, reflex tachycardia. Phenotalmine: reversible alpha blocker. Give to patients who eat tyramine containing foods on MAO inhibitor.

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5
Q

Right nasal hemianopia can be caused by?

A

Impingment on peri-chiasm of uncrossed fibers. For example, calficiation of the internal carotid artery can laterally impinge on the optic chiasm.

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6
Q

What is Chediak Highashi syndrome

A

Defect in lysosomal trafficking regulator gene (LYST), microtubule dysfunction in phagosome-lysosome fusion A/R. Sx: Recurrent pyogenic infections by staph and strep, partial albinism, peripheral neuropathy, progressive neurodegeneratino, infilitrative lymphohistiocytosis. Findings: Giant granules in neutrophils and platelets. Pan cytopenia, mild coagulation defects

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7
Q

What are the most common causes of acute pancreatitis

A

Alcohol and gallstones

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8
Q

What are some indicators of chronic alcohol consumption/alcoholic hepatatitis

A

AST:ALT ratio >2, macrocytosis, elevated GGT - indirect indicators of chronic alcohol consumption.May be due secondary to bad diet (low Vit B12 or folate) but can also be unrelated to diet/ related to toxic effects on the bone marrow.

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9
Q

What is a major pathogen in burn patients?

A

Pseudomonas aeruginosa

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10
Q

What drugs are effective against pseudonomas

A

Few specific penicillins (ticarcillin, piperacillin), cephalosporins (ceftazidime, cefepime). Some aminoglycosides (amikacin, tobramycin, gentamicin), fluoroquinolones (ciprofloxacin, levofloxcacin), and carabanepams (impinem, meropenem), monobactam (aztreonam) are also effective.

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11
Q

Infection with mycoplasma pneumonaie causes what kind of blood pathology?

A

Causes mild anemia. This is because ther eis antigenic similarity between M pneumonia cell membrane antigens and RBC cell membrane antigens. The antibodies against this antigen is called “cold agglutins” because they cause RBCs to agglutinate in lower temperatures. Can also cause Steven johnson sydrome, rarely

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12
Q

What is the most common cause of hyatid cysts? Where do they occur? What should you avoid doing?

A

Echinococcus granulosis - tapeworms. Occurs in indivduals frome endemic regions (like australiz, med countries, middle east, iceland, NZ), or from SW US with sheep and dog exposure (these animals participate in tapeworm life cycle). Most commonly occur in the liver. do not aspirate. spilled contents may cause anaphylaxis.

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13
Q

What is the DOC for long term prevention of recurrent venous thromboembolism

A

Warfarin/coumadin. Monitor with PT. Inhibits vit K dependent glutamate carboxylation of glutamic acid results in 2, 7, 9, 10.

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14
Q

Parvoviruses are what kind of DNA viruses

A

Single stranded, non-enveloped DNA Viruses

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15
Q

Aplastic crisis in patients with Sickle cell is usually caused by?

A

Aplastic crisis - persistently decreased reticulocyte count/insufficient response to anemia. Due to parvovirus infection which has a predilication for the bone marrow. Destroys erythroid precursor cells by this virus and dimishes the number of reticulocytes available to replace deformed/removed erythrocytes

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16
Q

What is the function of 16s rRNA in prokaryotic ribosomes?

A

Found in 30S ribosomal subunit. 16s rRNA contains sequence complementary to the Shine Delgarno equence on mRNA. Binding of these two is necessary for initiation of protein translation.

17
Q

What liver specific enzyme facilities the use of TAG breakdown products as intermediates in energy generation and glucose synthesis?

A

Glycerol kinase

18
Q

Respiratory distress, diffuse neuro impairment like confusion, upper body petechial rash within days of several long bone fractures is indicative of?

A

Fat Embolism syndrome. See multiple fat emboli in the pulmonaryy vascular. Stains black with osmium tetroxide.

19
Q

What are the topical vitamin D drugs used to treat psoriasis? What is the MOA?

A

Calcipotriene, calcitriol, tacalcitol bind to vitamin D receptor and INHIBIT kertinocyte proliferation, stimulate keritoncyte differentiation.

20
Q

Wht is the MOA of 6 mercaptopurine and azathioprine. 6 mercaptopurine is metabolized by?

A

Azathioprine is a metabolic precursor of 6MP - cytotoxic purine analog. Decreases de novo purine synthesis. Metabolized by xanthine oxidase. If you use allopurinol, a xanthine oxidase inhibitor, must adjust dosage of 6 mercaptopurine

21
Q

Why should you wait for a couple of weeks between stopping an MAO inhibitor and starting an SSRI?

A

Combined MAO inhibitor and SSRi can cause too much serotonin and can lead to serotonin syndrome. Need to wait a couple of weeks for MAO to be regenerated and then can start SSRI

22
Q

Histologic hallmark of rickets?

A

Unmineralized matrix, widened osteoid seams = osteiod accumulation around trabeculae. Clinical - bowed legs, rachicitc rosary (bony prominence at costochondral junction), indendentaions in lower ribs (Harrion’s sulci), softening of skul (craniotabes), growth regardation

23
Q

Excretion of large amounts of fructose in urine is indicative of?

A

Essential fructosuria

24
Q

In patients with esential fructosuria, what is the disroder? Also, how is fructose then metabolized?

A

Fructokinase deficiency (inability to convert fructose to fructose 1 phosphate). Large amounts excreted in urine. Fructose can be converted by hexokinase to Frcutose 6 phosphate, a glycolytic intermediate

25
Q

Methylomalonic aciduria results from?

A

= increased levels of methymalonyl CoA - due to deficiency of methylmalonyl CoA mutase (isomerization reactions that transforms methylmalonyl CoA to succinyl CoA that can enter the TCA cycle)

26
Q

Most patients with acute tubular necrosis expeirence what in their recovery?

A

Re-epitheliization of tubules

27
Q

What is an impaired upward gase called?

A

Parinaud syndrome

28
Q

Parinaud syndrome is most consistent with tumor of what region?

A

Pineal tumors

29
Q

Pineal region is the most common location of?

A

Brain germinomas which are histologically similar to testicular seminomas

30
Q

What is the MOA of calcineurin. Where is it found in?

A

Found in T cells. Once T cells are setimulated, calcineurin is activation which dephosphorylates NFAT-P. NFAT then enters the nucleus where it binds to the promoter of IL-2. IL-2 stimulates the growth and differentiation of T cells.