| Literature DB >> 18711298 |
K V Kanodia1, A V Vanikar, R D Patel, P R Shah, M Nagpal, A Firoz, J Falodia, P Kasat, H L Trivedi.
Abstract
Collapsing glomerulopathy (CG), characterized histologically by segmental/global glomerular capillary collapse, podocyte hypertrophy and hypercellularity and tubulo-interstitial injury; is characterized clinically by massive proteinuria and rapid progressive renal failure. CG is known to recur in renal allograft and rarely de novo. We report de novo CG 3 years post-transplant in a patient who received renal allograft from haplo-identical type donor.Entities:
Mesh:
Substances:
Year: 2008 PMID: 18711298
Source DB: PubMed Journal: Saudi J Kidney Dis Transpl ISSN: 1319-2442