| Literature DB >> 12169874 |
Yoshihiro Akashi1, Masayuki Inoh, Naoyuki Gamo, Makoto Kinashi, Seiichi Ohbayashi, Hayashi Miyake, Noriyuki Kurata.
Abstract
A 43-year-old woman was admitted to our hospital for myalgic pain and erythema of the face and thighs. She had been diagnosed with dermatomyositis at another hospital 8 years earlier and proteinuria had developed suddenly. Renal histological examination revealed membranous nephropathy. Membranous nephropathy associated with dermatomyositis is very rare. To date, malignant disease has not been detected in our patient, but the serum level of CA125, a tumor marker, has been elevated to 1,097 U/ml. The increased CA125 level is related to the degree of proteinuria and after prednisolone and cyclosporine therapy, proteinuria and the CA125 level gradually decreased. Copyright 2002 S. Karger AG, BaselEntities:
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Year: 2002 PMID: 12169874 DOI: 10.1159/000065233
Source DB: PubMed Journal: Am J Nephrol ISSN: 0250-8095 Impact factor: 3.754