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虹膜痣(科根 - 里斯)综合征:光镜和电镜观察

The iris naevus (Cogan-Reese) syndrome: light and electron microscopic observations.

作者信息

Eagle R C, Font R L, Yanoff M, Fine B S

出版信息

Br J Ophthalmol. 1980 Jun;64(6):446-52. doi: 10.1136/bjo.64.6.446.

Abstract

The light and electron micrscopic findings in an eye enucleated from a 38-year-old woman with iris naevus (Cogan-Reese) syndrome are presented. The clinical manifestations of this disease, namely, iridic stromal matting, iridic nodule formation, and unilateral angle-closure glaucoma, appear to be secondary to an endothelial membrane on the anterior surface of the iris. The iris naevus syndrome is now thought to represent one end of the clinical spectrum of an iridocorneal endothelial syndrome which also includes those clinical entities classified previously as Chandler's syndrome and essential iris atrophy.

摘要

本文展示了从一名患有虹膜痣(科根 - 里斯)综合征的38岁女性摘除的眼球的光镜和电镜检查结果。该疾病的临床表现,即虹膜基质模糊、虹膜结节形成和单侧闭角型青光眼,似乎继发于虹膜前表面的内皮膜。虹膜痣综合征现在被认为是虹膜角膜内皮综合征临床谱系的一端,该综合征还包括先前归类为钱德勒综合征和原发性虹膜萎缩的临床实体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f087/1043726/fb3e218b3df0/brjopthal00198-0064-a.jpg

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