Membranoproliferative glomerulonephritis associated with hypocomplementemic urticarial vasculitis after complete remission of membranous nephropathy

被引:10
作者
Saeki, T
Ueno, M
Shimada, H
Nishi, S
Imai, N
Miyamura, S
Gejou, F
Arakawa, M
机构
[1] Nagaoka Red Cross Hosp, Dept Internal Med, Nagaoka, Niigata 9402085, Japan
[2] Niigata Univ, Sch Med, Dept Med 2, Niigata, Japan
来源
NEPHRON | 2001年 / 88卷 / 02期
关键词
hypocomplementemic urticarial vasculitis; membranoproliferative glomerulonephritis; membranous nephropathy; steroid therapy;
D O I
10.1159/000045981
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
A 49-year-old-man developed proteinuria in 1978. He was diagnosed as having membranous nephropathy by renal biopsy and was treated with prednisolone. The proteinuria disappeared completely and the treatment was stopped. In 1995, after complete remission, he developed nephrotic syndrome with chronic urticaria and hypocomplementemia, Renal biopsy revealed membranoproliferative glomerulonephritis (type I) and skin biopsy showed leukocytoclastic vasculitis, which was compatible with hypocomplementemic vasculitis syndrome. Steroid therapy was very effective. Copyright (C) 2001 S. Karger AG, Basel.
引用
收藏
页码:174 / 177
页数:4
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