| Literature DB >> 15283187 |
Mai Tomioka1, Fumihiko Hinoshita, Naoko Miyauchi, Yurika Akiyama, Shigeki Saima, Michiaki Hiroe.
Abstract
A 64-year-old woman with scleroderma without marked dermatological change developed anti-neutrophil cytoplasmic autoantibody (ANCA)-related renal failure. She had neither malignant hypertension nor elevation of plasma renin concentration. Renal biopsy showed crescentic glomerulonephritis (pauci-immune type) and the myeloperoxidase-specific anti-neutrophil cytoplasmic autoantibody (MPO-ANCA) titer was found to be elevated to 757 IU/ml. Methylprednisolone pulse therapy followed by oral prednisolone effectively suppressed renal failure and lowered the MPO-ANCA titer. We believe this is a rare case of ANCA-related renal failure in a patient with scleroderma without marked dermatological change.Entities:
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Year: 2004 PMID: 15283187 DOI: 10.2169/internalmedicine.43.496
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.271