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23 Cards in this Set

  • Front
  • Back
Lumpy-bumpy =
Acute proliferative GN
(poststeptococcal)
What is the crescent from Cr-GN made of?
Fibrin
Macrophages, monocytes
Parietal cells of BC
Cr-GN with (+) anti=GM Ab's and Linear deposits of IgG and C3
Type I
Cr-GN with "lumpy bumpy" IF, and post-streptococcal,SLE, IgA Nephropathy, or Henoch schonlein
Type II
Cr-GN with (-) anti-GBM, (-) IC's, (+) ANCA and Wegeners granulomatosis
Type III
Elevated ASO titers, LOW serum complement =
Acute post-streptococcal GN
Types of Nephritic Syndrome
Acute prolif/poststrep GN
anti-GBM disease/Goodpastures
RPGN
IgA Nephropathy
Membranoproliferative GN
Alport's
Anti-GBM Disease with pulmonary involvement =
Goodpasture's
Berger's =
IgA Nephropathy
MCC of GN in the World
IgA Nephropathy (Berger's)
Hallmark of IgA nephropathy
IgA deposition in the mesangium
IgA nephropathy may be a variant of -
Henoch-Schonlein purpura
Difference betw. Henoch and IgA
IgA is only kidney involvement.
Henoch is systemic. Both have IgA deposits
In IgA nephropathy, where are the deposits?
in the MESANGIUM
What conditions are IgA nephropathy associated with?
And Why?
Celiac Sprue (intestinal mucosal defects)
Liver disease (defective hepatobiliary clearance of IgA)
Henoch-shonlein
Recurrent hematuria during/after URI =
IgA Nephropathy
Nephritis + Deafness + Eye disorders (lens dislocation, posterior cataracts, corneal dystrophy)
Alport's
BM show foci of thickening w/ splitting and lamination of lamina densa, basket weave appearance
Alport's
Which gene is mutated in Alport's? and what protein does that gene encode?
Gene: COL4A5

Alpha 5 chain of collagen Type 4
MCC of nephrotic syndrome in children
Minimal change disease
Disease with Nephrotic syndrome
Membranous GN, Minimal Change disease, Focal segmental, membranoproliferative
(+) C3 nephritic factor
Type 2 MPGN
Splitting of BM (tram tracking) on PAS or silver stain
Membranoproliferative GN