9/7/12 Flashcards

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1
Q

Mycoplasma require a medium enriched in ______ to grow in culture.

A

cholesterol

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2
Q

S. pneumoniae can be differentiated from S. viridans by its sensitivity to which Abx used in bacterial culture?

A

optochin

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3
Q

What type of hemolysis do S. penumoniae and S. viridans display?

A

alpha (partial hemolysis)

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4
Q

Which pneumonia-causing oganism requires a medium enriched in L-cysteine?

A

Legionella

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5
Q

What is the mechnism of the diplopia that is often the presenting symptom of multiple sclerosis?

A

MLF syndrome (internuclear ophthalmoplegia) - loss of myelination of the MLF, which coordinates lateral conjugate gaze.

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6
Q

How is the definitive Dx of MS made?

A

Visualization of sclerotic plaques on MRI.

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7
Q

Briefly summarize the 5 steps of MS pathogenesis.

A
  1. axon demyelination
  2. destruction of oligodendrocytes
  3. lipid-laden MΦs
  4. fibrillary astrocytosis
  5. infiltration by lymphocytes and monocytes
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8
Q

What is the function of gp120?

A

binding to CD4 receptor

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9
Q

What is the function of gp41?

A

fusion w/target cell

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10
Q

What are the 3 structural genes of HIV? Which one becomes gp160?

A

gag, pol, and env

env

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11
Q

The HIV structural gene gag codes for the protein _______, which makes up the _______.

A

p24; viral capsid

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12
Q

What kind of kidney damage may be caused by bacterial endocarditis? What is the mediator of the is damage?

A

acute diffuse proliferative glomerulonephritis

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13
Q

What mediates the acute diffuse proliferative glomerulonephritis caused in some cases of bacterial endocarditis?

A

circulating immune complexes that deposit in the subepithelium or mesangium

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14
Q

Why are glomeruli in PSGN referred to as “hypercellular”?

A

endothelial and mesangial proliferation & NΦ infiltrate

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15
Q

Where do the immune complexes of PSGN deposit?

A

subepithelial

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16
Q

Where do the immune complexes of SLE deposit?

A

subendothelial (too large to pass GBM)

17
Q

What are the top 3 causes of crescentic glomerulonephritis?

A
  1. Goodpasture syndrome
  2. Wegener’s granulomatosis
  3. Microscopic polyangiitis
18
Q

What is the most common Ag in Wegener’s granulomatosis?

A

c-ANCA

19
Q

What is the Ag seen in microscopic polyangiitis?

A

p-ANCA

20
Q

What is the Tx for Wegener’s granulomatosis?

A

cyclophosphamide

21
Q

What is seen on electron microscopy in IgA nephropathy?

A

mesangial immune complexes

22
Q

How does Alport Syndrome manifest in EM of the glomeruli?

A

Split basement membrane

23
Q

What is the etiology of Alport syndrome?

A

mutation in type IV collagen

24
Q

What are the clinical manifestations of Alport syndrome?

A

glomerulonephritis, nerve disorders, ocular disorders, deafness

25
Q

How is Alport syndrome inherited?

A

X-linked

26
Q

What is the primary reason for thiamine deficiency in alcoholics?

A

liver dysfunction

27
Q

What drug frequently used in A-fib will increase the circulating dose of warfarin?

A

amiodarone

28
Q

What is the main mechanism of amiodarone?

A

class III anti-arrhythmic (blocks K+ channels)