Idiopathic acute interstitial nephritis associated with uveitis.

N Yano, M Miyazaki, M Endoh, T Kuramoto, K Eguchi, M Yagame, Y Nomoto, H Sakai
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引用次数: 13

Abstract

A case of acute interstitial nephritis associated with uveitis is presented, An 18-year-old man developed uveitis followed by renal dysfunction. Moderate renal dysfunction (sCr 3.0 mg/dl), and increased levels of urinary beta 2 microglobulin (over 8,000 micrograms/I) were observed. Renal tissue obtained by open renal biopsy revealed severe infiltration of mononuclear cells in the tubulo-interstitial area. The majority of infiltrating cells were CD4-positive T cells demonstrated by immunoperoxidase staining, suggesting the involvement of T cell-mediated delayed hypersensitivity. Corticosteroid was effective against both uveitis and renal dysfunction. The possible pathogenesis of this syndrome is reviewed from the literature.

伴有葡萄膜炎的特发性急性间质性肾炎。
我们报告一例急性间质性肾炎合并葡萄膜炎,一名18岁男性,因葡萄膜炎并发肾功能不全。观察到中度肾功能障碍(sCr 3.0 mg/dl),尿β 2微球蛋白水平升高(超过8000微克/分升)。肾组织开放活检显示肾小管间质区单核细胞严重浸润。免疫过氧化物酶染色显示,大多数浸润细胞为cd4阳性T细胞,提示与T细胞介导的延迟超敏反应有关。皮质类固醇对葡萄膜炎和肾功能障碍均有效。本文从文献综述了该综合征可能的发病机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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