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31 Cards in this Set
- Front
- Back
Acute Poststreptococcal glomerulonephritis:
-Mechanism |
Type III Hypersensitivity
H/o recent Strep infection (impetigo, cellulitis, pharyngitis) |
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Acute Poststreptococcal glomerulonephritis:
-Light microscopy |
Glomeruli enlarged and hypercellular
Neutrophils "Lumpy Bumpy" |
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Acute Poststreptococcal glomerulonephritis:
-Electron Microscopy |
Subepithelial humps
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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 |
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Acute Poststreptococcal glomerulonephritis:
-Immunoflourescnece |
Granular pattern
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Rapidly Progressive (crescentic) glomerulonephritis:
- Light microscopy - Immunoflurescence |
-LM & IF: crescent-moon shape
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Goodpasture's syndrome
-sxs -Mechanism -Immunofluorescence |
Type II hypersensitivity:
Nephritic syndrome: HTN, oliguria, hematuria, azotemia *HEMOPTYSIS, HEMATURIA IF: linear pattern (anti-GBM antibodies) |
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Rapidly Progressive (crescentic) glomerulonephritis:
- sxs |
Sxs: hematuria, HTN, oliguria, azotemia
*Rapidly course to RENAL FAILURE (# of crescents ~ prognosis) |
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Membranoproliferative glomerulonephritis
*Sxs |
Sxs: hematuria, HTN, oliguria, azotemia
*Slowly progresses to renal failure |
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Membranoproliferative glomerulonephritis:
*EM |
EM: subendothelial humps
"TRAM TRACKS" |
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IgA Neprophathy
-other name? -nephritic or nephrotic? |
Berger's disease
Nephritic |
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IgA Neprophathy:
- mild or severe disease? - IF and EM findings? |
Mild disease. Often post-infectious.
-IF and EM: mesangial deposits of IgA |
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Alport's Syndrome
-mutation in what? -sxs? |
-Mutation in Collagen IV
-sxs: nerve deafness and ocular disorders |
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Alport syndrome:
-pathology? |
Split basement membrane
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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 |
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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 |
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Nephrotic syndromes:
generic sxs (4) |
1. massive proteinuria (>3g/day) - frothy urine
2. hypoalbuminemia 3. peripheral and periorbital edema 4. Hyperlipidemia/lipiduria |
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Membranous glomerulonephritis:
LM findings |
Diffuse capillary and basement membrane thickening
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Membranous glomerulonephritis:
IF: findings |
Granular pattern
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Membranous glomerulonephritis:
EM findings |
"Spike and Dome"
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Most common cause of childhood nephrotic syndrome.
Hint - responds well to steroids |
Minimal Change disease
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Minimal Change disease
-other name |
Lipoid nephrosis
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Minimal Change disease
-LM and EM findings |
LM: normal glomeruli
EM: foot process effacement |
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Most common cause of Adult nephrotic syndrome
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Membranous glomerulonephritis
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Focal segmental glomerular sclerosis
-Features -LM findings |
*more severe in HIV pts
-LM: Segmental sclerosis and hyalinosis |
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Diabetic Nephropathy:
LM: |
-Kimmelstiel Wilson "wire loop' lesions
-basement membrane thickening |
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SLE Nephrotic syndrome
- how many patterns of involvement? |
FIVE
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SLE Nephrotic syndrome
- in membranous glomerulonephritis pattern, what are the LM findings? |
Wire loop lesion with subepithelial depositis
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Amyloidosis:
-associated morbidity (4) |
-Multiple myeloma
-Chronic conditions -TB -Rheumatic arthritis |
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Amyloidosis:
IF findings |
Congo red stain
Apple green birefringence |
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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 |