Renal 3 Flashcards

1
Q

Name 4 key features (symptoms/lab tests) of nephrotic syndrome

A
  1. generalied edema
  2. high grade proteinuria (>3.5 g/24 hrs)
  3. hypoalbuminemia (<3g/dL plasma)
  4. hyperlipidemia
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2
Q

Name three primary causes of nephrotic syndrome and one secondary cause

A
primary
-minimal change disease
-focal segmental glomerulosclerosis
-membranous nephropathy
seconary
-diabetic nephropathy
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3
Q

What’s the most common cause of nephrotic syndrome in children?

A

minimal change disease (looks normal on light and IF microscopy)

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4
Q

How would you treat minimal change disease?

A

steroids

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5
Q

What would you see on EM microscopy for minimal change disease?

A

epithelial foot process effacement

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6
Q

Focal segmental glomerulosclerosis is a form of _____ syndrome and presents most often in ______

A
  1. nephrotic syndrome

2. african americans

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7
Q

What would you see microscopically in focal segmental glomerulosclerosis (FSGS)?

A

-microscopic hematuria

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8
Q

T/F- hypertension is rarely seen in focal segmental glomerulosclerosis

A

False, it is often seen

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9
Q

Describe the microscopic appearance of glomeruli in FSGS for light, IF, and EM

A

LM: segmental sclerosis
IF: mild IgM and C3 or could be negative
EM: diffuse epithelial cell injury

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10
Q

T/F- FSGS always responds to steroids just like minimal change disease

A

False, FSGS response is variable to steroids, unlike MCD which almost always responds to steroids

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11
Q

Where will immune deposits be located in membranous nephropathy?

A

Sub-epithelial deposits causing “spikes” by silver stain

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12
Q

T/F- chronic membranous nephropathy presents with waxing and waning of proteinuria

A

True

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13
Q

Name the gene associated with membranous nephropathy (recently discovered)

A

PLA2R

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14
Q

Name the conditions associated with membranous nephropathy in each category:

  1. Autoimmune
  2. Infectious disease
  3. Drugs
A

Autoimmune= Lupus
Infectious disease= hepatitis B
Drugs= Penicillamine

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15
Q

T/F- Diabetic nephropathy usually presents with a linear glomerulosclerosis

A

False, it is a nodular glomerularsclerosis

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16
Q

Define thrombotic microangiopathy

A

Pathological entity characterized by endothelial injury resulting in widespread thrombosis in the microcirculation and arteriolar necrosis.

17
Q

What 3 things does thrombotic microangiopathy lead to?

A
  1. microangiopathic hemolytic anemia
  2. thrombocytopenia
  3. in some cases, renal failure
18
Q

What will you see histologically for hrombotic microangiopathy?

A

fragmented red cells in arteriolar wall, fibrinoid necrosis of arteriole, and onion skinning of arteriole

19
Q

What are the 3 common causes of thrombotic microangiopathy?

A
  1. hemolytic uremic syndrome/Thrombotic thrombocytopenia
  2. malignant hypertension
  3. anti-phospholipid syndrome
20
Q

What chromosome is the autosomal dominant mutation in ADPKD present on (polycystin-1 protein)?

A

chr 16

21
Q

What decade of life does autosomal dominant polycystic kidney disease present with symptoms?

A

4th

22
Q

What causes subarachnoid hemorrhage in pts with ADPKD?

A

berry/saccular anuerysms in the circle of willis