Abstract
Rapidly progressive glomerulonephritis (RPGN) is a clinical syndrome characterized by quick and propagative deterioration of renal function with loosing 50% or more of renal function within three months. RGPN is associated with cellular crescents in more than 50% of glomeruli; hence it is called crescentic glomerulonephritis. We report a 47-year-old patient who presents with RPGN associated with fibrillary glomerulonephritis (FGN) and positive antiglomerular basement membrane (anti-GBM) antibody. In conclusion, FGN should be suspected in any case of RPGN presents with a nephrotic range of proteinuria. Although light microscopic and immunofluorescent studies in a renal biopsy are essential, electron microscopic study is the gold standard in establishing the diagnosis of FGN. FGN and Anti-GBM disease can co-exist as causes of RPGN.
| Original language | English |
|---|---|
| Pages (from-to) | 8716-8723 |
| Number of pages | 8 |
| Journal | International Journal of Clinical and Experimental Pathology |
| Volume | 9 |
| Issue number | 8 |
| Publication status | Published - 2016 |
Keywords
- Anti-glomerular basement membrane disease
- Crescentic glomerulonephritis
- Fibrillary glomerulonephritis
- Nephrotic syndrome
ASJC Scopus subject areas
- Pathology and Forensic Medicine
- Histology
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