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Membranoproliferative glomerulonephritis associated with hypocomplementemic urticarial vasculitis after complete
1Department of Internal Medicine, Nagaoka Red Cross Hospital, Nagaoka, Japan. saekit@nagoka.jrc.or.jp
Nephron
|June 16, 2001
Abstract:
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.