Nephrotic Syndrome Flashcards

1
Q

Nephrotic syndrome is characterized by ___________.

A

high protein urine; hypoalbuminemia; edema; hyperlipidemia; lipiduria

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2
Q

Nephrologists think that ____________ causes nephrotic syndrome.

A

destruction of podocytes or inter-podocyte proteins

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3
Q

Nephrotic syndrome leads to increased risk of ____________.

A

coagulation (decreased anti-thrombin), infections (loss of Ig), and decreased vitamin D

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4
Q

These treatments are all indicated for nephrotic syndrome: ______________.

A
BP control
Diuretics
Low salt diets
Cholesterol lowering drugs
ACE inhibitors 
Vitamin D supplements
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5
Q

Minimal change disease has a peak incidence from age _____ to ______.

A

2; 8

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6
Q

Podocytes express ________ in minimal change disease.

A

CD80

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7
Q

Hereditary nephrotic syndrome presents in ___________.

A

infancy

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8
Q

Hereditary nephrotic syndrome does not respond to _____; it requires _________.

A

steroids; transplantation

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9
Q

Those with relapsing minimal change disease are often given ____________.

A

cytoxan

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10
Q

What are some associations with focal segmental glomerulosclerosis?

A
Being African American
Age 20-40
Sickle cell
HIV
APOL1polymorphisms
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11
Q

What are some treatments for focal segmental glomerulosclerosis?

A

Cyclosporine

Corticosteroids

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12
Q

HIV glomerulosclerosis presents with _________.

A

tubular dilations

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13
Q

Membranous nephropathy can be caused by ___________.

A
HBV
Cancer
Idiopathic
Heavy metals
SLE
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14
Q

Histologically, membranous nephropathy is characterized by ____________.

A

thickened glomberular membrane with immune complex deposits, projections on silver stain, and subepithelial deposits

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15
Q

What are treatments for membranous nephropathy?

A

Coricosteroids

Cytoxan

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16
Q

___________ have interdigitating foot processes.

A

Podocytes

17
Q

What protein connects podocytes together (across their slit diaphragms)?

A

Nephrin

18
Q

What are the five kinds of primary renal nephrotic syndrome?

A
Focal segmental glomerulosclerosis
Membranoproliferative glomerulonephritis
Membranous nephropathy
Minimal change disease
Hereditary nephrotic syndrome
19
Q

Lipiduria presents as ___________ in the urine.

A

“Maltese crosses”

20
Q

What are the two most common kinds of nephrotic syndrome in adults? And in children?

A

Adults: membranous nephropathy (most common in fifth and sixth decades) and FSGS
Children: minimal change disease and a tie between membranous nephropathy and FSGS

21
Q

Histologically, minimal change disease will be ______________.

A

negative to immunofluorescence and light microscopy, but will show podocyte foot fusion on electron micrographs

22
Q

FSGS is usually __________.

A

idiopathic

23
Q

HIV nephropathy responds to __________ treatment.

A

HAART

24
Q

What percent of AIDS patients have HIV nephropathy?

A

5% - 10%

25
Q

What type of nephrotic syndrome is associated with HCV?

A

Membranproliferative nephropathy

26
Q

What cell secretes the glomerular basement membrane?

A

The mesangial cell

27
Q

Excretion of greater than 30 mg per day of albumin is indicative of ____________.

A

glomerular damage; less than 300 mg per day is not detectable with urine dipsticks and is called microalbuminuria

28
Q

___________ presents with subendothelial deposits.

A

Membranoproliferative glomerulonephritis

29
Q

Minimal change disease is twice as common in _________.

A

males

30
Q

Over seventy percent of idiopathic __________ is due to antibodies to phospholipases on podocytes.

A

membranous nephropathy

31
Q

Hereditary nephrotic syndrome can be treated with _________.

A

ACE inhibitors (to reduce proteinuria)