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16 Cards in this Set

  • Front
  • Back
Name all the nephritic syndromes
1. Acute poststreptococcal glomerulonephritis
2. Rapidly progressive glomerulonephritis (crescentic)
3. Diffuse proliferative glomerulonephritis
4. Berger's Disease
5. Alport's Syndrome (also has ESRD and hearing loss b/c of poorly formed basement membranes)
Name all the nephrotic syndromes
1. Membranous glomerulonephritis
2. Minimal Change disease
3. Amyloidosis
4. Diabetic glomerulonephropathy
5. Focal segmental glomerulosclerosis
6. Membranoproliferative glomerulonephritis
What does is mean when a glomerulo disease ends in "itis"
immune COMPLEX disease (Type III hypersensitivity)
Define nephritic syndrome
1. hematuria
2. RBC casts in urine
3. proteinuria < 3.5g/day

(also azotemia, oliguria, and HTN)
Define nephrotic syndrome
1. Proteinuria > 3.5g/day
2. Lipid casts/hyperlipidemia/"frothy" urine
3. edema
Findings and cause (if known) for Acute Poststreptococcal glomerulonephritis
Sx: Kids, periorbital edema, resolves spontaneously
LM: "lumpy bumpy", sub-epithelial humps
IF: granular

Cause: after strep infection
Findings and cause (if known) for Rapidly Progressive glomerulonephritis
Sx: Usually male, lung also involved
LM: crescent moon shape
IF: linear (Goodpastures, Type II hypersensitivity is the most common cause) *this breaks goljan's "itis" rule

Cause can also be Wegener's (c-ANCA) or Microscopic polyarteritis (p-ANCA)
Findings and cause (if known) for Diffuse Proliferative glomerulonephritis
Sx: #1 death in SLE (could also present as nephrotic)
LM: "wire looping"
IF: granular

Cause: SLE
Findings and cause (if known) for Berger's Disease
Sx: aka "IgA Glomerulopathy", follows Upper Resp. Infection!
LM: Immune complexes in mesangium
Findings and cause (if known) for Alport's Syndrome
Sx: Nerve disorder, sight and hearing problems
LM: split basement membrane
Findings and cause (if known) for membranous glomerulonephritis
Sx: #1 adult glomerulonephropathy (also SLE when it presents as nephrotic)
LM: spike and dome, thickend GBM
IF: granular

Cause: various DRUGS, infections, or SLE
Findings and cause (if known) for minimum change disease
Sx: #1 kid nephrotic syndrome, presents after illness, tx with steroids

LM: normal
IF: normal
EM: fused podocytes

Cause: various DRUGS, infections, or SLE
Findings and cause (if known) for amyloidosis
Sx: Assc with mult myeloma, chronic conditions, TB, RA
LM: condo red stain, apple-green birefringence
Findings and cause (if known) for diabetic glomerulonephropathy
Sx: diabetic sx's
LM: Kimmelstiel-Wilson "wire loop" lesions

Cause: Non-enzymatic glycosylation of GBM causes increased GFR and mesangial damage
Findings and cause (if known) for focal segmental glomerulosclerosis
Sx: HIV!!!
LM: segmental sclerosis and hyalinosis

Cause: HIV...bad prognosis
Findings and cause (if known) for membranoproliferative glomerulonephritis
Sx's: HBV assc!!! (could also be HCV), progresses to CRF
LM: Sub-endothelial immune complexes
IF: Granular
EM: "Tram-track appearence"