膜性肾病
肾病综合征
足细胞
自身抗体
发病机制
血栓反应素
病理
组织病理学
医学
免疫学
肾小球肾炎
抗原
抗体
内科学
蛋白尿
肾
基质金属蛋白酶
金属蛋白酶
作者
Qi Cai,Allen R. Hendricks
标识
DOI:10.1053/j.semdp.2020.01.001
摘要
Membranous nephropathy (MN) is a common cause of nephrotic syndrome in adults. Over the last decade important research discoveries have revealed that most “idiopathic” cases are caused by autoantibodies to podocyte antigens including phospholipase A2 receptor (PLA2R) and thrombospondin type 1 domain containing 7A (THSD7A). In this review, we will discuss the histopathology of primary MN, recent revelations regarding pathogenesis, and ancillary tests.
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