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29 Cards in this Set
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Nephritic syndrome
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acute/subacute inflamm process
hematuria, proteinuria and sometimes RBC casts may burn out to nephrotic syn |
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nephrotic syndrome
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heavy proteinuria and edema, also urine fat
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causes of glomerular dx #3
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1. antigen/antibody
2. antibody against basement membrane 3. idiopathic |
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what is FeNa value in glomerulopathy?
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always <1%
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what are the 3 components of the glomerular wall
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1. endothelial cells
2. glomerular BM 3. slit pores betw the epithelial foot processes |
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3 findings on light/electron microscopy of renal bx
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1. subepithelial deposits
2. sub endothelial deposits 3. mesangial deposits |
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what glomerular diseases have subepithelial deposits on renal bx?
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membranous nephropathy
postinfectious GN |
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What glomerular diseases have subendothelial deposits on renal bx?
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diffuse, proliferative, lupus nephritis, and membranoproliferative GN
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What glomerular disease(s) have mesangial deposits on renal bx?
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IgA nephropathy
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Nephritic urine sediment
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active--dysmorphic RBCs and WBCs and casts of RBC, WBC and granular material
variable proteinuria |
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Nephritic syndrome causes:
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postinfectious GN, IgA nephropathy, lupus nephritis
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Nephrotic syndrome urine sediment
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usu nl, see heavy proteinuria and urine fat
also hypogammaglobulinemia--which makes them prone to infection w encapsulated orgs, also hypercoagulable also hyperlipidemia |
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glomerular dx and low complement
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lupus, PIGN, freq w membranoproliferative, cryoglobulin GN, shunt nephritis, endocarditis
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causes of RPGN
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Goodpastures
idiopathic, SLE vasculitis(wegeners, PAn) |
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3 categories of RPGN by pathology
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1. immune complex
2. pauci-immune dx 3. anti-GBM antibody dx |
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urine findings RPGN
path/glomeruli |
protein, RBC casts
>50% glomeruli have crescents--if inflamm crescents will respond to tx, if fibrous irreversible |
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What are the first 2 antibody tests you order in workup of RBGN?
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first order Anti_GBM and ANCa
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RPGN + anti GBM + pulmonary hemorrhage
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Goodpastures
if no pul hemorrhage think just anti -GBM GN |
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RPGN + +ANCA
3 possibilities |
1. Wegeners
2. PAN 3. idiopathic ANCA + crescentic GN |
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RPGN
-anti-GBM and -ANCA think: |
IC mediated problems
lupus nephritis--ck anti DS DNA ab post strep GN cryoglobulinemic Gn-ck cryo levels and complement-should be low) |
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RPGN tx
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corticosteroids + cyclophosphamide or azathioprine
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RPGN from Goodpastures or cryoglobulinemic GN tx:
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plasmapheresis followed by alkylating agent
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PIGN etiol
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usu nonstrep causes
freq septicemia or viruses subepithelial deposits AB/Ag reaction IgG C3 |
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PIGN labs
latency period? |
low complement which returns to nl in 6-8 wks
latency betw infection/PIGN is 1-6 wks |
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PIGN tx
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abtics/underlying infection
prorgresses to severe renal failure only if infections persists |
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Membranoproliferative gn or MPGN
assoc w ?infection complement level? |
assoc w Hep C
complement low |
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why is this called "double" GN?
what is complement level? |
both basement membrane chgs and cell proliferation.
BM chgs--can cause nephrotic syn cell prolif--is the nephritic component low complement |
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when does complement level return to normal in MPGN?
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stays low indefinitely
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MPGN tx
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kids prednisone
adults ASA and oral dipyridamole if MPGN assoc w hep c interferon |