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A RISE IN ANTINEUTROPHIL CYTOPLASMIC ANTIBODY IN A PATIENT WITH SYSTEMIC VASCULITIS IN REMISSION
被引:5
|作者:
KANAME, S
UCHIDA, S
MINODA, S
ARIMURA, Y
NAGASAWA, T
ASANO, S
OGATA, E
机构:
[1] UNIV TOKYO,FAC MED,DEPT INTERNAL MED 3,TOKYO 113,JAPAN
[2] KYORIN UNIV,SCH MED,DEPT INTERNAL MED 1,TOKYO,JAPAN
[3] UNIV TOKYO,FAC MED,DEPT INTERNAL MED 4,TOKYO 113,JAPAN
来源:
NEPHRON
|
1994年
/
68卷
/
03期
关键词:
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY;
PREDNISOLONE;
CYCLOPHOSPHAMIDE;
MIZORIBINE;
WEGENERS GRANULOMATOSIS;
NECROTIZING GLOMERULONEPHRITIS;
LEUKOCYTOCLASTIC ANGIITIS;
IMMUNOBLOT;
D O I:
10.1159/000188405
中图分类号:
R5 [内科学];
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号:
1002 ;
100201 ;
摘要:
We report a 42-year-old man who showed alveolar hemorrhage and glomerulonephritis as well as episcleritis and skin rash. He had an extremely high titer of cytoplasm-staining antineutrophil cytoplasmic antibody (C-ANCA) and was diagnosed as having systemic vasculitis based on histological findings of kidney and skin biopsies. After immunosuppressive therapy clinical manifestations resolved within several weeks and C-ANCA titers commensurably declined. C-ANCA titers, however, increased again and remained high despite clinical remission. In general, there is a close relationship between ANCA titers and clinical activities in ANCA-associated diseases, but they displayed a large discrepancy in this patient. Indeed, the serum of the patient in remission contained the antibody against 29-kD neutrophil extracts which was detected by immunoblot analysis. These findings suggest that C-ANCA may not necessarily be, by itself, pathogenetic for the development of the vasculitis.
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页码:380 / 384
页数:5
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