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IgA肾病与白细胞破碎性皮肤血管炎并存并与强直性脊柱炎相关:一例报告

Coexisting IgA nephropathy and leukocytoclastic cutaneous vasculitis associated with ankylosing spondylitis: a case report.

作者信息

Hsu C M, Kuo S Y, Chu S J, Shih T Y, Chen A, Huang G S, Chang D M

机构信息

Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan, R.O.C.

出版信息

Zhonghua Yi Xue Za Zhi (Taipei). 1995 Jan;55(1):83-8.

PMID:7712401
Abstract

A patient with ankylosing spondylitis and coexisting IgA nephropathy and leukocytoclastic cutaneous vasculitis is described. Renal biopsy demonstrated mesangial proliferative glomerulonephritis with prominent IgA, C3 and fibrin deposition in the glomeruli. Simultaneously, leukocytoclastic cutaneous vasculitis with prominent IgG, IgA and C3 deposition of dermal vessel wall was also observed in the skin biopsy specimen. Such associations have been previously reported in only four cases. This report once again indicates that antigenic mucosal stimulation may play an important role in the pathogenesis of ankylosing spondylitis.

摘要

本文描述了一名患有强直性脊柱炎,同时合并IgA肾病和白细胞破碎性皮肤血管炎的患者。肾活检显示为系膜增生性肾小球肾炎,肾小球内有显著的IgA、C3和纤维蛋白沉积。同时,在皮肤活检标本中也观察到白细胞破碎性皮肤血管炎,真皮血管壁有显著的IgG、IgA和C3沉积。此前仅有4例报道过这种关联。本报告再次表明,抗原性黏膜刺激可能在强直性脊柱炎的发病机制中起重要作用。

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