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17 Cards in this Set
- Front
- Back
What are some of the general distinctions between nephrotic syndrome and nephritic syndrome?
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Nephritis has less of the classic features like hematuria, proteinuria, edema, and MORE of the stuff suggesting a more disruptive lesion.
(RBC casts, etc.) - note that we're really talking about glomerular nephritis, not tubular interstitial nephritis here. |
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What are basement membrane nephropathies and why can they be probelmatic in terms of dx?
- example? - chief presentaion sx? |
they can mimic the more inflammatory nephritic syndrome sx (can mimic IgA nephropathy (type of nephritis))
- Thin GBM nephropathy - asymptomatic hematuria --> note that while ~1/3 of asx. hematuria is caused by IgA nephropahty, most pts with IgA don't have it. |
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Basement membrane nephropathies are ______ disorders caused by abnormalities in _______.
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hereditary dz caused by defects in type IV collagen.
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What is Alport's syndrome?
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type of glomerula basement membrane nephropathy that shows malformed (not thin like thin GBM) basement membrane due to defect in TIV collagen. It has a worse prog than Thin GBM.
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Linear IF staining - think waht?
paucity of glomerular IF staining? |
Anti GBM dz
immune complex dz ANCA |
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Actue glomerulo nephritis with incrased cells inluding numerous marginated and infiltrating neutrophils resulting in an acute diffuse proliferative glomerularnephrtitis. Thiank what? Most often caused by?
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acute posinfectious Glom. nephritis
strep or staph |
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for post infectious (acute) nephritis, what chances should you look for on EM?
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subepithelial immune complex humplike deposits.
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If the infection manages to last for a long time --> chronic, what type of dz pattern is seen developing?
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membranoproliferative Glomerulonephritis.
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What two features are seen in membranoproliferative glomerulonephritis? Is this how IgA nephropathy always presents?
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hypercellularity and thick capillary walls.
No, it can range from histologically normal gomeruli to crescenteric/sclerosis. Just depends on when you catch it. |
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What is IgA nephropathy?
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glom dz w/ IgA dominant or codominant mesangial immunoglobulin.
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What is the most common golmerulonephritis in the world? More likely in AA?
Age of presentation? |
IgA nephropathy
No, less, very uncommon. typically middle=aged (20s-40s) |
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- Episodic macroscopic hematuria
- asd. hematuria and proteinuria - rapildly progressive glomerulonephritis - chronic renal failure - nephrotic syndrome - actue renal failure with gross hematuria all are what? |
patterns of possible clinical presentation of some of the nephritisis.
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Episodic Macroscopic hematuria w/ Sydpharyngitic glomerulonephritis is a presentation most common in which age group?
- why is the timing critical? |
children
- in IgA nephropathy, the URI/GI infection occurs around the SAME TIME as the hematuria... in post-infectious, it's a few weeks later, at least. |
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Are those with IgA nephropathy presenting with asymptomatic hematuria/proteinuria at lower or higher risk of eventually progression to sclerosis when comparted with those that present with episodic gross hematuria?
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higher risk.
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Place the following in one of three categories re: presenting sx: those w/o hypocomplementemia, those with only C3 hypocomplementemia, those with both C3 and C4 hypocomplementemia:
- Henoch-Schonlein purpura - MPGN - ANCA-associated SVV - IgA nephritis - Endocartditis GN (including shunt nephrosis) - Lupus - Cryoglobulinemia DN - Postinfectious GN |
none:
- Anca, IgA, Henoch C3: PostInf. GN Endocarditis GN MPGN Both: Lupus Cryoglobulinemic DN |
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Worldwide, what is the most common cause of Type I MPGN? Prog?
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Hep C
- maj of pts with idiopathic MPGN progress - may improve if there is an identiable cause and that cause is tx'ed. |
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hematuria
HTN renal insufficiency some edema - makes you think either nephritic or nephrotic? predominant proteinuria edema if it lasts, renal insufficienty if it lasts, HTN nephritic/nephrotic |
- nephritic
- nephrotic |