©The Author(s) 2018.
World J Transplantation. Oct 22, 2018; 8(6): 203-219
Published online Oct 22, 2018. doi: 10.5500/wjt.v8.i6.203
Published online Oct 22, 2018. doi: 10.5500/wjt.v8.i6.203
Table 1 Morphological features of C3 glomerulopathy
| Morphological features of C3G | |
| Light microscopy | Active lesions |
| Mesangial expansion with or without hypercellularity | |
| Endocapillary hypercellularity including monocytes and/or neutrophils | |
| Capillary wall thickening with double contours (combination of capillary wall thickening + mesangial increase is referred to as a membranoproliferative pattern) | |
| Fibrinoid necrosis | |
| Cellular/fibrocellular crescents | |
| Chronic lesions | |
| Segmental or global glomerulosclerosis | |
| Fibrous crescents | |
| IF microscopy | Typically dominant C3 staining |
| Electron microscopy | DDD: Dense osmiophilic mesangial and intramembranous electron dense deposits. |
| C3GN: Amorphous mesangial with or without capillary wall deposits including subendothelial, intramembranous and subepithelial EDD | |
| Subepithelial “humps” may be seen in both DDD and C3GN |
- Citation: Abbas F, El Kossi M, Kim JJ, Shaheen IS, Sharma A, Halawa A. Complement-mediated renal diseases after kidney transplantation - current diagnostic and therapeutic options in de novo and recurrent diseases. World J Transplantation 2018; 8(6): 203-219
- URL: https://www.wjgnet.com/2220-3230/full/v8/i6/203.htm
- DOI: https://dx.doi.org/10.5500/wjt.v8.i6.203