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31 Cards in this Set

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Acute Poststreptococcal glomerulonephritis:
-Mechanism
Type III Hypersensitivity
H/o recent Strep infection (impetigo, cellulitis, pharyngitis)
Acute Poststreptococcal glomerulonephritis:
-Light microscopy
Glomeruli enlarged and hypercellular
Neutrophils
"Lumpy Bumpy"
Acute Poststreptococcal glomerulonephritis:
-Electron Microscopy
Subepithelial humps
Acute Poststreptococcal glomerulonephritis:
-symptoms
-Tx
Nephritic: Hematuria, hypertension, oliguia, azotemia
*Children, Periperal & PERIORBITAL EDEMA
*cola-colored urine
Tx: resolves spontaneously but can give loop diuretic for HTN/edema and vasodilators
Acute Poststreptococcal glomerulonephritis:
-Immunoflourescnece
Granular pattern
Rapidly Progressive (crescentic) glomerulonephritis:
- Light microscopy
- Immunoflurescence
-LM & IF: crescent-moon shape
Goodpasture's syndrome
-sxs
-Mechanism
-Immunofluorescence
Type II hypersensitivity:
Nephritic syndrome: HTN, oliguria, hematuria, azotemia
*HEMOPTYSIS, HEMATURIA

IF: linear pattern (anti-GBM antibodies)
Rapidly Progressive (crescentic) glomerulonephritis:
- sxs
Sxs: hematuria, HTN, oliguria, azotemia

*Rapidly course to RENAL FAILURE (# of crescents ~ prognosis)
Membranoproliferative glomerulonephritis
*Sxs
Sxs: hematuria, HTN, oliguria, azotemia
*Slowly progresses to renal failure
Membranoproliferative glomerulonephritis:
*EM
EM: subendothelial humps
"TRAM TRACKS"
IgA Neprophathy
-other name?
-nephritic or nephrotic?
Berger's disease
Nephritic
IgA Neprophathy:
- mild or severe disease?
- IF and EM findings?
Mild disease. Often post-infectious.

-IF and EM: mesangial deposits of IgA
Alport's Syndrome
-mutation in what?
-sxs?
-Mutation in Collagen IV

-sxs: nerve deafness and ocular disorders
Alport syndrome:
-pathology?
Split basement membrane
Nephritic Syndromes:
-name them (6)
1. Acute post-strep glomerulonephritis
2. Rapidly progressive (crescentic) glomerulonephritis
3. Goodpasture's syndrome
4. Membranoproliferative glomerulonephritis
5. IgA nephropathy (berger's dz)
6. Alport's syndrome
Nephrotic syndromes:
-name them (6)
1. Membranous glomerulonephritis
2. Minimal change disease (lipoid nephrosis)
3. Focal segmental glomerular sclerosis
4. Diabetic nephropathy
5. SLE (5 patterns)
6. Amyloidosis
Nephrotic syndromes:
generic sxs (4)
1. massive proteinuria (>3g/day) - frothy urine
2. hypoalbuminemia
3. peripheral and periorbital edema
4. Hyperlipidemia/lipiduria
Membranous glomerulonephritis:
LM findings
Diffuse capillary and basement membrane thickening
Membranous glomerulonephritis:
IF: findings
Granular pattern
Membranous glomerulonephritis:
EM findings
"Spike and Dome"
Most common cause of childhood nephrotic syndrome.
Hint - responds well to steroids
Minimal Change disease
Minimal Change disease
-other name
Lipoid nephrosis
Minimal Change disease
-LM and EM findings
LM: normal glomeruli
EM: foot process effacement
Most common cause of Adult nephrotic syndrome
Membranous glomerulonephritis
Focal segmental glomerular sclerosis
-Features
-LM findings
*more severe in HIV pts

-LM: Segmental sclerosis and hyalinosis
Diabetic Nephropathy:
LM:
-Kimmelstiel Wilson "wire loop' lesions
-basement membrane thickening
SLE Nephrotic syndrome
- how many patterns of involvement?
FIVE
SLE Nephrotic syndrome
- in membranous glomerulonephritis pattern, what are the LM findings?
Wire loop lesion with subepithelial depositis
Amyloidosis:
-associated morbidity (4)
-Multiple myeloma
-Chronic conditions
-TB
-Rheumatic arthritis
Amyloidosis:
IF findings
Congo red stain
Apple green birefringence
Nephrotic syndrome:
Pathophysiology
1. increased permeability of glomerular capillary wall -> massive protein loss in urine
2. decreased serum albumin -> edema
3. decreased circulating blood volume -> ADH, aldosterone -> increased Na and H20 retnetion ->edema
4. increased lipoprotein synthesis (liver compensates for hypoalbuminemia) -> hyperlipidemia ->lipiduria