A nephrologist is reviewing renal biopsy reports for four different adult patients who presented with various nephritic or nephrotic syndromes. To establish the correct diagnosis, match each specific glomerular disease with its most pathognomonic histological, immunofluorescence, or ultrastructural finding on renal biopsy.
- IgA nephropathy (Berger disease)Granular immunofluorescence pattern with prominent mesangial deposition of IgA and C3
- Membranous nephropathySubepithelial immune complex deposits with 'spike and dome' appearance on silver stain
- Goodpasture disease (anti-GBM disease)Linear immunofluorescence pattern with diffuse IgG deposition along the glomerular basement membrane
- Post-streptococcal glomerulonephritisEnlarged, hypercellular glomeruli with subepithelial electron-dense 'humps' on electron microscopy
Answer
IgA nephropathy matches with mesangial IgA deposition; Membranous nephropathy matches with 'spike and dome' appearance; Goodpasture disease matches with linear IgG deposition; Post-streptococcal glomerulonephritis matches with subepithelial 'humps'.
Establishing a definitive diagnosis for primary glomerular diseases relies heavily on identifying distinct biopsy findings. Goodpasture disease is unique for its linear immunofluorescence pattern caused by anti-GBM antibodies. Immune complex diseases produce granular patterns, but their specific location and appearance differentiate them: IgA nephropathy shows mesangial deposits, membranous nephropathy causes a subepithelial 'spike and dome' pattern due to basement membrane remodeling, and post-streptococcal glomerulonephritis presents with large subepithelial 'humps'.
Step-by-Step Solution
Key Concept
Histopathological and Immunofluorescence Diagnosis of Glomerular Diseases