| Literature DB >> 25275829 |
Di Wu1, Jin-Song Chen, Dong-Rui Cheng, Hao Chen, Xue Li, Shu-Ming Ji, Ke-Nan Xie, Xue-Feng Ni, Zhi-Hong Liu, Ji-Qiu Wen.
Abstract
Proliferative glomerulonephritis with monoclonal IgG deposits manifesting as a nephrotic syndrome recently has been described as a renal disease with the pathological features of mesangial and subendothelial deposits of monoclonal IgG. Eight cases of recurrent proliferative glomerulonephritis with monoclonal IgG deposits after a renal transplant have been reported. Almost all of these patients had a certain remission of proteinuria by steroids alone or with cyclophosphamide, and had further remission through other special treatments (ie, rituximab and plasmapheresis). We present a case of recurrent proliferative glomerulonephritis with monoclonal IgG deposits of the IgG3? subtype after a renal transplant, which was insensitive to pulse intravenous methyl-prednisolone and cyclophosphamide remitted by double filtration plasmapheresis. This case report reveals that recurrent proliferative glomerulo-nephritis with monoclonal IgG deposits may be insensitive to intravenous pulse therapy of methylprednisolone and cyclophosphamide. We advocate double filtration plasmapheresis as an effective treatment of proliferative glomerulo-nephritis with monoclonal IgG deposits on remission of proteinuria.Entities:
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Year: 2014 PMID: 25275829 DOI: 10.6002/ect.2014.0107
Source DB: PubMed Journal: Exp Clin Transplant ISSN: 1304-0855 Impact factor: 0.945