Nephritic syndrome Flashcards
Nephritic syndrome causes
Acute streptococcal GMN IgA nephropathy Alport syndrome Crescent GMN Diffuse proliferative GMN Membranoproliferative GMN
Electron microscopy: Subendothelial and sometimes intramembranous IgG based immune complexes with C3 deposition.
Diffuse Proliferative GMN
Mutation in type IV collagen and X-linked dominant
Alport syndrome
Thinning and splitting of glomerular basement membrane.
Alport syndrome
LM shows fibrin and plasma proteins (C3b), macrophage and monocytes
Crescent GMN
Associated with antibodies to alveolar membrane (good pastures syndrome) and type 2 hypersensitivity.
Crescent GMN
Occurs after group A streptococcal ( strep. pyrogens) infection, spontaneous resolution, usually occurs in children 2-4 years old, associated with hypersensitivity type 3
Acute poststreptococcal glomerulonephritis
Membranoproliferative GMN:
Type 1:
Disease associations
Diagnosis
Type 2:
Associations
Diagnosis
Type 1;
Hepatitis B or C
Idiopathic
Subendothelial deposits with granular IF
Type 2;
-Associated with C3 nephritic factor
(IgG antibody that stabilizes C3 convertase which leads to persistent compliment activation and ultimately decreased C3 levels)
-Intramembranous deposits “dense deposit disease”