| Literature DB >> 12135179 |
Togo Aoyama1, Takeshi Shimizu, Takatoshi Matsuo, Hisato Sakamoto, Kouju Kamata, Masaaki Higashihara, Hiroshi Tsuji, Hidekazu Shigematsu, Yutaka Kobayashi.
Abstract
A 37-year-old woman had been found to have proteinuria in October 1996. About 8 months later, the first renal biopsy was performed, revealing focal segmental necrotizing and crescentic glomerulonephritis. At that time, serum creatinine was 1.0 mg/dl and urinary protein 3+. In October 1999, laboratory tests revealed positivity for MPO-ANCA and a serum creatinine level of 1.42 mg/dl, anemia and proteinuria of 2+. A second renal biopsy showed almost the same histological findings. Accordingly, a diagnosis of MPO-ANCA positive glomerulonephritis was made. This patient was thought to be a rare case of MPO-ANCA-positive slowly progressive glomerulonephritis presenting focal segmental tuft necrosis and crescents.Entities:
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Year: 2002 PMID: 12135179 DOI: 10.2169/internalmedicine.41.458
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.271