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29 Cards in this Set

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