| Literature DB >> 18224274 |
Tatsuo Hashimoto1, Yoshiyuki Toya, Minoru Kihara, Machiko Yabana, Yoshiaki Inayama, Ken-Ichiro Tanaka, Kousaku Iwatsubo, Mai Yanagi, Jin Oshikawa, Toshiharu Kokuho, Tadashi Kuji, Shin-Ichiro Yoshida, Kouichi Tamura, Satoshi Umemura.
Abstract
A 65-year-old woman with a 48-year history of Behçet's disease associated with nephrotic syndrome is described. Immunofluorescence study revealed IgA nephropathy. Following treatment with an angiotensin II type-I receptor-blocker, an anti-platelet drug, and an HMG-CoA reductase inhibitor, accompanied by dietary restrictions of protein and sodium, proteinuria was markedly decreased. This report describes our experience with a rare entity of Behçet's disease complicated by nephrotic syndrome due to IgA nephropathy. Routine urine examination and renal biopsy are needed for the detection and diagnosis of renal problems with Behçet's disease.Entities:
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Year: 2008 PMID: 18224274 DOI: 10.1007/s10157-008-0029-6
Source DB: PubMed Journal: Clin Exp Nephrol ISSN: 1342-1751 Impact factor: 2.801