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IgA 肾病:简要综述。

IgA nephropathy: A brief review.

机构信息

Department of Pathology, Temple University Health System, Temple University Hospital, 3401 N. Broad St, Philadelphia, PA 19140, United States.

出版信息

Semin Diagn Pathol. 2020 May;37(3):143-147. doi: 10.1053/j.semdp.2020.03.001. Epub 2020 Mar 16.

Abstract

IgA nephropathy is a lifelong disease that is the most common primary glomerulopathy worldwide. It has a complicated and incompletely understood pathogenesis that is theorized as a four 'hit' process involving an improperly produced IgA. While it has a variety of histologic appearances, it is diagnosed by the presence of bright IgA deposits within the mesangium as seen on immunofluorescence and mesangial hypercellularity by light microscopy. This brief review explains the varied histologic features that are important in the diagnosis of IgA nephropathy and the calculation of the MEST-C score that was first introduced by the 2009 Oxford Classification working group.

摘要

IgA 肾病是一种终身性疾病,是全球最常见的原发性肾小球疾病。其发病机制复杂且尚未完全阐明,理论上认为是涉及异常产生 IgA 的四步“打击”过程。虽然它具有多种组织学表现,但通过免疫荧光检查系膜内存在明亮的 IgA 沉积物和光镜下系膜细胞增多来诊断。本综述解释了在 IgA 肾病诊断中重要的各种组织学特征,以及首次由 2009 年牛津分类工作组引入的 MEST-C 评分的计算方法。

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