Rapidly Progressive Glomerulonephritis (RPGN)
RPGN has three primary pathophysiologic causes differentiated by immunofluorescence
Immune Complex Mediated (granular staining):
• Low Complement: Post-strep GN, Lupus Nephritis, Cryoglobulinemia, Endocarditis, Idiopathic
• Normal Complement: IgA nephropathy, Henoch-SchonIein Purpura
Anti-GBM antibodies (linear staining):
• Limited to Kidney: Anti-GBM Glomerulonephritis
• With associated pulmonary involvement: Anti-GBM Disease (Goodpasture's)
Pauci-immune mediated (Negative IF):
• PR3-ANCA (C-ANCA): GPA >>> MPA > eGPA
• MPO-ANCA (P-ANCA): eGPA, MPA >>> GPA
Stanford Internal Medicine Chiefs @StanfordChiefs
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