IgA肾病伴白细胞破碎性血管炎。

IgA nephropathy with leucocytoclastic vasculitis.

作者信息

Wei Lin-Yan, Liu Chao, Zhang Ya-Li, Li Guo-Liang

机构信息

1 Department of Cardiovascular Medicine, First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.

2 Department of Nephrology, First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.

出版信息

J Int Med Res. 2018 Jul;46(7):3009-3014. doi: 10.1177/0300060518775814. Epub 2018 Jun 10.

DOI:10.1177/0300060518775814

PMID:29888629

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6124258/

Abstract

Leucocytoclastic vasculitis is a rare type of allergic disease caused by immune complexes. IgA nephropathy is a glomerulopathy characterized by recurrent episodes of gross haematuria or microscopic haematuria and IgA deposition in the glomerular mesangial region. IgA nephropathy complicating leucocytoclastic vasculitis is rare documented. We present a case of IgA nephropathy in a 47-year-old woman with leucocytoclastic vasculitis and discuss the clinical and pathological data, aiming to promote the diagnosis and treatment of this specific clinical manifestation.

摘要

白细胞破碎性血管炎是一种由免疫复合物引起的罕见过敏性疾病。IgA肾病是一种肾小球病，其特征为反复出现肉眼血尿或镜下血尿，以及IgA在肾小球系膜区沉积。IgA肾病并发白细胞破碎性血管炎鲜有文献记载。我们报告一例47岁患有白细胞破碎性血管炎的女性IgA肾病病例，并讨论其临床和病理资料，旨在促进对这种特殊临床表现的诊断和治疗。