UWorld Test 5/30/2014 Flashcards

1
Q

Majority of patients with MG have what kind of mass>

A

thymoma / thymic hyperplasia

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2
Q

The majority of cancers in the head and neck are? Where do they tend to develop?

A

Squamous cell carcinomas. Oral cavity - ventral dongue, floor of the mouth, lower lip, soft palate and gingivae are the most common locations

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3
Q

What is the MOA for nitroglycerin. How does it affect heart rate, contractility, end diastolic volume, blood pressure, ejection time and myocardial oxygen consumption

A

Decreases angina by overall reduction in myocardial oxygen consumption. Increases vascular smooth muscle relaxation, especially in the veins compared to arteries => vendodilators. => decrease venous return and end diastolic volume. There is reflexive increase in heart rate and contractiliy which can be treated with beta blockers. ejection time and myocardial oxygen consumption decrease

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4
Q

What is alleleic heterogeniety?

A

Different mutations in the SAME genetic locus causes similar phenotypes. Example Duchenne and Becker muscular dystrophy.

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5
Q

Superior rectain vein drains into what? Which further drains into?

A

Superior rectal => inferior mesenteric => splenic vein

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6
Q

Splenic vein meets with the superior menesteric vein to form?

A

Portal vein

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7
Q

What is achondroplasia?

A

Constitutive action of FGFR3 gene => leads to inhibition of chondrocyte proliferation and failure of enchondral ossification which means failure of long bone growth. => dwarfirsm. >85% are sporadic though also shows some a/d inheritance. a/w advanced paternal age

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8
Q

What is Bruton’s agammaglobulinemia? What is the inheritance?

A

B cell disorder. X linked.BTK gene defect => Impaired intracellular messaging. No B cell maturation. Leads to recurrent bacterial and enteroviral infections after 6 months. Lab: absent CD19+ cells, decreased pro-B, decreased Ig of all classes. Abscent/scanty lymph nodes

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9
Q

Proteins designated for the ER have what?

A

N terminal peptide signaling sequences. These N terminal sequences are translated in the cytosol and are rapidly recognized by signal recognition particles which halt translation and target the ribosome to protein pores in the RER. Once bound, the SRP dissaciates, translation continues with the pp being fed into the RER. SRP are hydrophobic and are compose of 15-20 a.a.

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10
Q

What is articular cartilage? What kind of cartilage is found in this? What is the main collagen type?

A

Cartilage found on bone in joint spaces. Hyaline cartilage is found in articular cartilage. The main type of collagen is collagen type II.

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11
Q

Collagen can be stained with what?

A

Safranin O stains CARTILAGE mucin and mast cell granules red.

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12
Q

Pheochromocytomas results in elevated levels of?

A

Serum catecholamines, metanephrine, and vanillymandelic acid.

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13
Q

What is the normal range for 1) PaO2 2) PaCO2 3) Bicarb and 4)pH

A

1) 80-95mmHg 2) 35-45mmHg 3) 22-26mEq/L 4)7.35-7.45

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14
Q

What happens with pulmonary embolism

A

Pulmonary embolism => V/Q mismatch => hypoxemia => hyperventilation => respiratory alkalosis. High pH, low pAO2 and paCO2

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15
Q

What kind of expression is NFtype1

A

A/D, 100% penetrance with variable expressivity

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16
Q

Phenoxybenzamine vs phentolamine

A

Both are non selective alpha blockers. Phenoxybenzamine is NON-COMPETITIVE IRREVERSIBLE alpha blocker with a LONG HALF LIFE (24 hours with effects lasting 3-4 days). Used for pheochromocytomas to avoid hypertensive crisis. Phentolamine is a reversible alpha blocker with a shorter half life.

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17
Q

What are the toxicities of amiodarone

A

Interstitial pneumonitis - progressive dyspnea and nonproductive cough. Causes arrythmias, photosensitivity, hepatic injurity, thryoid abnormalitie (amiodarone is 40% iodine by weight), ocular changes, bluish gray skin discoloration. Corneal deposits.

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18
Q

What is palmitoylation?

A

Process by which fatty acids are covalently anchored to plasma membrane cystein residues => increases hydrophobicity of a protein

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19
Q

CFTR function in sweat glands?

A

Normally reabsorbs NaCl. Mutated CFTR => diminishes this and increases sweat tonicity.

20
Q

CFTR function in respiratory and intestinal epithelieum

A

Normal CFTR allows for active chloride secretion. Mutated => reduces luminal chloride secretion and increases luminal sodium reabsorption. Water follows sodium => and depletes the water content of the surface fluid layer. Isotonic low volume surface fluid layer leads to production of thick viscous secretions.

21
Q

What is the level of testosterone in the seminferous tubules relative to testosterone in circulation?

A

Seminiferous tubules and epididymis must have more in order for spermatogenesis and sperm maturation to occur.

22
Q

How is a high concentration of testosterone in the seminferous tubules achieved?

A

Sertoli cells synthesize and secrete androgen binding protein. ABP binds to testosterone and DHT and makes them less lipophilic, thereby concentrating them to the luminal fluid

23
Q

Superior cervical sympathetic ganglion innervates

A

Lacrimal, salivary, radial muscle of iris, tarsal muscle

24
Q

Thoracic cervical sympathetic trunk innervates

A

Sweat glands among others

25
Q

Metabolic derangements with DKA

A

Metabolic acidosis, hyperkalemia, hyponatremia, glycosuria, ketonemia, hyperglycemia. Block 2 of UWSA1 Item 5/33 of “correct” answers has amazing explanation

26
Q

What cells synthesize leukotrienes

A

Eosinophils and mast cells

27
Q

Efflux pumping by resistant bacteria requires

A

ATP. Relies on H+ gradient for energy to pump drug out

28
Q

Round ligament of the uterus is a remant of what? What does it connect/pass through?

A

Guburnaculum. Passes through the inguiinal ligament. Connects uterus to labia major. Upper part of the gubuernaculum becomes proper ovarian ligament which connects the uterus to the ovary

29
Q

What is platelet activating factor? What signaling pathway does it use?

A

Promotes platelet aggregation through the Gq/IP3 pathways. Excess PAF can cause bronchoconstriction, vasocontriction

30
Q

Rapid infusion of what leads to red man syndrome?

A

vancomycin. Widespread histamine release via nonspecific mast cell degranulation. NOT an IgE mediated reaction.

31
Q

Know what epidural hematoma vs subdural hematoma vs subarachnoid hemorrhage vs intraparenchymal hemorrhage look like

A

Epidural hematoma = convex shape, subdural hematoma = crescent shape, SAH = blood in the sucli/ventricles, intraparenchymal = intraparenchyma/often basal ganglia

32
Q

SAH usually occurs due to the rupture of? What are they a/w?

A

Saccular (berry aneuryms) or AVMs. Saccular aneuryms are associated with ADPKD, Marafan’s and ehler’s Danos

33
Q

What is the most common presentation of recurrent hemorrhagic stroke?

A

Cerebral amyloid angiopathy

34
Q

Recurrent lobar hemorrhages in an elderly patient is most associated with what?

A

Cerebral amyloid angiopathy. Beta amyloid depsots in vessel walls, weakening them. They are NOT associated with systemic amyloidosis. They tend to occur in the cerebral hemispheres (lobar strokes) and involve smaller areas of the brain parenchyma. VS hypertensive strokes are larger and tend to occur in the basal ganglia

35
Q

What are signs of thalamic syndrome?

A

Thalamic syndrome is when there is an ischemic or hemorrhage event that affects the VPL and VPM of the thalamus leading to complete contralateral sensation loss. Although there are no motor deficits per say, propioception loss can be so severe it can affect ambulation

36
Q

What is the most common cause of asesptic meningitis?

A

Enterovirus

37
Q

What are enteroviruses?

A

SS+RNA, naked, icosahedraol, Picornaviridae - include poliovirus, echovirus, coxsacie virus A and B, hep A. most common cause of aseptic Poliovirus can also affect lower motor function by affecting the anterior horn

38
Q

What presents in von Hippel Landau disease

A

Cavernous hemangiomas (benign, self involuting tumor of the endothelial cells that line the blood vessels) in skin, organs, mucosa; congenital cysts/neoplasms of kidney, pancreas, liver; bilateral renal cell carcinoma, and HEMANGIOBLASTOMAS in retina, cerebellum, brain stem; pheochromocytomas. A/D.

39
Q

What happens to area of brain infarct following thrombosis or embolism?

A

Infart => neuronal cell death (macroscopically changes seen within 12 hours) => neutrphils move into start eating up => microglia come in 3-5 days. Microglia eat the disintegrating neurons => abundance of phagocytic myelin breakdown causes abundance of lipids

40
Q

Paraneoplastic syndrome process? How can it affect the brain?

A

Antibodies against tumor cells start cross reacting against body’s own tissue. Can produce paraneoplastic cerebellar degeneration which is autoimmune. Common places of paraneoplastic cancrs = lung, breast, ovary, uterus, lymphoma

41
Q

What is a rare neurologic complication of measles?

A

Subacute sclerosing encephalitis. Thought to be a strain of measles that does not that the antigen M protein, therefore antibodies doesn’t effectively clear it. Antibodies to the M protein in titers are missing. There are high titers of antibodies to measles and oligoclonal bands of immunoglobulins

42
Q

What test should be done if one suspects temporal arteritis?

A

ESR is uniformly elevated often >100mm/hr. biopsy is needed for diagnosis. Steroid treatment should be started asap to prevent vision loss.

43
Q

What do these following viruses bind to? 1) CMV 2) EBV 3) HIV 4) Rabies 5) Rhinovirus

A

1) cellular integrins 2) CD21 3) CD4, CXCR4, CCR5 4) Nicotinich Ach R 5) ICAM-1 (CD54)

44
Q

Which pediatric tumors arise in the cerebellum?

A

Pilocytic astromas and medulloblastomas

45
Q

What are the microscopic findings of medulloblastomas?

A

Sheets of primitive cells with many mitotic figures. They are “primitive neuroectoerdermal tumors” (PNETS).Sheets of small cells with deeply basophilic nuclei and scant cytoplasm (small, round blue cells).