Nephrotic Syndrome Flashcards

1
Q

Minimal Change Disease pathology

A

Effacement of podocytes/foot processes on EM

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2
Q
Minimal Change Disease findings
MCC of what?
Urine finding 
S & S (3)
What/who to look for?
A
MCC of nephrotic syndrome in children
Proteinuria
Hypoalbuminemia
Edema (periorbital, sacral, and scrotal)
HTN

**Look for sudden onset edema in a child with hx of infections and thrombotic events

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3
Q

Minimal Change Disease tx

A

Glucocorticoids (excellent prognosis)

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4
Q

Focal Segmental Glomeruloscerlosis etiology

A
  1. Idiopathic
  2. IV drug use
  3. HIV
  4. Obesity
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5
Q

Focal Segmental Glomeruloscerlosis pathology

Who to look for?

A

Sclerosis is FOCAL (<50% glomeruli) and SEGMENTAL (only part of each glomeruli)
**Look for an African American man with uncontrolled HTN

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6
Q

Focal Segmental Glomeruloscerlosis findings:
which patients (3)
Urine
Biopsy finding

A
  • Increased prevalence among African Americans, Latinos, and HIV patients
  • Microscopic hematuria
  • Biopsy shows sclerosis in capillary tufts
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7
Q

Focal Segmental Glomeruloscerlosis treatment (4)

A
  1. Glucocorticoid
  2. ACE-i
  3. Statin
  4. +/- cyclosporine
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8
Q
Membranous nephropathy History/PE
Associated with (4)
A

Associated with solid-tumor malignancies, infections (HBV, malaria), autoimmune (SLE), and drugs (NSAIDs, gold)

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9
Q

Membranous nephropathy histology

A

“Spike and Dome” appearance due to granular deposits of IgG and C3 at the basement membrane

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10
Q

Membranous nephropathy treatment (4)

A
  1. ACE-i
  2. Statin
  3. Cyclophosphamide
  4. Prednisone
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11
Q

Membranoproliferative glomerulonephritis (MPGN) pathology (3)

A
  1. “Tram Track” appearance
  2. Subendothelial “humps” of IgG on GBM–> formation of second GBM
  3. Mesangial cells proliferate between the GBMs
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12
Q

Membranoproliferative glomerulonephritis (MPGN) clinical associations (3)

A
  1. SLE
  2. Subacute bacterial endocarditis
  3. Hepatitis C
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13
Q

Membranoproliferative glomerulonephritis (MPGN) treatment (3)

A
  1. Treat underlying cause
  2. Glucocorticoids
  3. +/- cyclophosphamide
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14
Q

Diabetic nephropathy pathology (2)

A
  1. Diffuse hyalinization

2. Nodular glomerularsclerosis (Kimmelstiel-Wilson nodules)

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15
Q

Diabetic nephropathy history and labs (3)

A
  1. Hx of poorly controlled diabetes
  2. Thickened GBM
  3. Increased mesangial matrix
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16
Q

Diabetic nephropathy treatment (3)

A
  1. ACE-i or ARB
  2. Aggressive BP control
  3. Aggressive glycemic control
17
Q

Renal amyloidosis pathology

A

Abnormal amyloid proteins deposit in tissues (heart, kidney, liver, brain, muscle)

18
Q

Renal amyloidosis clinical associations

A

Multiple myeloma

Chronic inflammatory diseases (RA, TB, IBD)

19
Q

Renal amyloidosis treatment (2)

A
  1. Prednisone
  2. Melphalan
  3. BMT if multiple myeloma is causative
20
Q

Renal amyloidosis histology

A

Congo red stain shows “apple-green birefringence”

21
Q

Lupus nephritis (or nephrosis)

A

SLE –> variable changes:

  • immune deposits
  • proliferation of mesangial cells
  • thickening of GBM
22
Q

Lupus findings

A

Proteinuria
+ANA
+Anti-dsDNA antibodies
**LM: endothelial deposits cause “wire loops”

23
Q

Lupus treatment (4)

A
  1. Glucocorticoid
  2. ACE-i
  3. Statin
  4. Immunosuppressant (cyclophosphamide)