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特发性结节性肾小球硬化伴纤维帽形成 1 例

A case of idiopathic nodular glomerulosclerosis with fibrin caps.

机构信息

Division of Nephrology, Kyoto Min-Iren Chuo Hospital, 16-1 Kasuga-cho, Nishinokyo, Nakagyo-ku, Kyoto 604-8453, Japan.

出版信息

Clin Exp Nephrol. 2011 Dec;15(6):937-41. doi: 10.1007/s10157-011-0513-2. Epub 2011 Aug 17.

Abstract

We report a case of idiopathic nodular glomerulosclerosis (ING) mimicking diabetic Kimmelstiel-Wilson glomerulopathy. A 72-year-old man suffering from nephritic syndrome and renal dysfunction had no prior history of diabetes mellitus, but had impaired glucose tolerance and a history of hypertension and smoking. A kidney biopsy showed increased mesangial matrix with Kimmelstiel-Wilson-like nodules, glomerular basement membrane thickening and capillary microaneurysms. Additionally, a large amount of fibrin caps detectable as electron-dense subendothelial material by electron microscopy were observed. Although ING with fibrin caps has been rarely reported, the large number of fibrin caps seen in this case may be due to the advanced clinical stage.

摘要

我们报告了一例特发性结节性肾小球硬化症(ING)模拟糖尿病 Kimmelstiel-Wilson 肾小球病。一位 72 岁的男性患有肾病综合征和肾功能障碍,没有糖尿病史,但有葡萄糖耐量受损和高血压及吸烟史。肾活检显示系膜基质增多,伴有 Kimmelstiel-Wilson 样结节、肾小球基底膜增厚和毛细血管微动脉瘤。此外,还观察到大量纤维蛋白帽,电镜下可见电子致密的内皮下物质。虽然有纤维蛋白帽的 ING 很少见报道,但本例中观察到的大量纤维蛋白帽可能是由于疾病处于晚期。

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