Nephrotic Syndromes Flashcards

1
Q

List 6 Purely Nephrotic Syndromes

A
  1. ) Minimal-Change Disease
  2. ) Focal-Segmental Glomerulosclerosis
  3. ) Membranous Nephropathy
  4. ) Diabetic Nephropathy
  5. ) Lupus Nephritis
  6. ) Renal Amyloidosis
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2
Q

List 2 Mixed Nephrotic/Nephritic Syndromes

A
  1. ) Membranoproliferative Nephropathy Type I

2. ) Membranoproliferative Nephropathy Type II/III

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3
Q

Describe the Hx, Labs, and Treatment/Prognosis of:

Minimal Change Disease

A

Description/Hx: Most common cause of nephritic syndrome in children. Can happen in adults. Associated with malignancy, esp. Hodgkin’s and NSAID use. Sudden onset with tendency for thrombotic events and edema.

Labs: LM = normal, EM = fusion of epithelial foot processes (podocyte fusion) with lipid-laden renal cortices.

Tx/Prognosis: Steroids, excellent prognosis.

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4
Q

Describe the Hx, Labs, and Treatment/Prognosis of:

Focal Segmental Glomerulosclerosis

A

Description/Hx: Idiopathic, IV drug use, HIV, obesity. Most common nephrotic syn. in adults. Typical patient is young AA man w/ hypertension.

Labs: Microscopic hematuria; biopsy shows sclerosis in capillary tufts.

Tx/Prognosis: Prednisone, cytotoxic therapy, ACEI/ARBs to decrease proteinuria.

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5
Q

Describe the Hx, Labs, and Treatment/Prognosis of:

Membranous Nephropathy

A

Description/Hx: Accounts for ~30% of adult nephrotic syn. Ass. with solid-tumor malignancies, infections (HBV, Malaria), autoimmunty (SLE), NSAIDs.

Labs: “Spike and Dome” on IM. Granular deposits of IgG and C3 at the basement membrane.

Tx/Prognosis: Prednisone and cytotoxic therapy.

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6
Q

Describe the Hx, Labs, and Treatment/Prognosis of:

Diabetic Nephropathy

A

Description/Hx: Diffuse hyalinazation and nodular glomerulosclerosis ( Kimmelstiel-Wilson lesions). Longstanding diabetics.

Labs: Thickened GBM and mesangial matrix.

Tx/Prognosis: Tight control of BG, ACEIs/ARBs

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7
Q

Describe the Hx, Labs, and Treatment/Prognosis of:

Lupus Nephritis

A

Description/Hx: Associated with Lupus, the prognosis of which is ass. with the degree of renal damage. Can present as mixed nephrotic/itic.

Labs: Mesangial proliferations, subendothelial IC deposition.

Tx/Prognosis: Prednisone and cytotoxic therapy may slow disease progression.

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8
Q

Describe the Hx, Labs, and Treatment/Prognosis of:

Renal Amyloidosis

A

Description/Hx: Pts. have multiple myeloma or chronic inflammatory disease (RH, MTb).

Labs: Nodular glomerulosclerosis with fibrils on EM, apple-green birefringence with congo red stain.

Tx/Prognosis: Prednisone and Melphalan.

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9
Q

Describe the Hx, Labs, and Treatment/Prognosis of:

Type I Mixed Nephrotic/ritic Syndrome (Membranoproliferative Nephropathy)

A

Description/Hx: Ass w/ HBV, HCV, SLE, and subacute bacterial endocarditis. Cyroglobulinemia

Labs: “Tram-Track” double-layered basement membrane. Subendothelial and mesangial deposits of IC. Low C3.

Tx/Prognosis: Corticosteroids and cytotoxic agents.

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10
Q

Describe the Hx, Labs, and Treatment/Prognosis of:
Type II/III Mixed Nephrotic/ritic Syndrome
(Membranoproliferative Nephropathy)

A

Description/Hx: Idiopathic

Labs: Intramembranous dense deposits. Occurs by way of C3 nephritic factor.

Tx/Prognosis: Corticosteroids and cytotoxic agents.

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11
Q

Primary Causes of FSGS

A

AA & Hispanics, obesity, HIV, Heroin

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12
Q

Primary Causes of Membranous Nephropathy

A

Adenocarcinoma (Breast, Lung), NSAIDs, HBV, SLE

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13
Q

Primary Causes of Membranoproliferative GS

A

HBV, HCV, Lipodystrophy

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14
Q

Primary Causes of Minimal Change Disease

A

NSAIDs, Lymphoma

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15
Q

Primary Causes of IgA Nephropathy

A

URI

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