Match the following glomerular diseases with their classic renal biopsy or immunofluorescence findings.
- Minimal change diseaseDiffuse effacement of podocyte foot processes without immune complex deposition
- Membranous nephropathyThickened capillary loops with subepithelial 'spike and dome' deposits
- IgA nephropathyGranular mesangial immune complex deposits, classically presenting with episodic hematuria
- Goodpasture syndromeLinear immunoglobulin deposition along the glomerular basement membrane
Answer
Minimal change disease pairs with podocyte effacement; Membranous nephropathy pairs with subepithelial 'spike and dome' deposits; IgA nephropathy pairs with mesangial immune complex deposits; and Goodpasture syndrome pairs with linear immunoglobulin deposition.
Each glomerular disease has a pathognomonic finding on biopsy. Minimal change disease requires electron microscopy to see podocyte effacement. Membranous nephropathy shows subepithelial 'spike and dome' deposits. IgA nephropathy localizes to the mesangium. Goodpasture syndrome is distinguished by linear anti-GBM antibody deposition.
Step-by-Step Solution
Key Concept
Glomerular Disease Histopathology and Immunofluorescence Patterns
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