Sherrard E S, Frangoulis M A, Muir M G
Institute of Ophthalmology, London, England.
Cornea. 1991 May;10(3):233-43. doi: 10.1097/00003226-199105000-00009.
The iridocorneal endothelial (ICE) syndrome is potentially a blinding condition as a result of glaucoma and/or corneal decompensation. The basic pathology seems to be in the corneal endothelium, which many studies confirm takes on a characteristic slit lamp appearance of hammered silver and image reversal with the specular microscope. The origin and morphology of the abnormal cells are unknown. Many histopathological studies of keratoplasty and trabeculectomy specimens reveal as many cell types. This paper reports some general and specular microscopical data from 57 cases of the syndrome, argues that the reason for the variety of histopathological findings in other studies is due to poor sampling of the study material, deduces the morphology of the abnormal cells on specular microscopical criteria, and compares the specular and scanning electron microscopical images in one case with those of other reports. It is tentatively concluded that the appearance of the abnormal cells is a function of their three-dimensional shape and that they produce blister-like vesicles that rupture, collapse, and eventually invaginate.
虹膜角膜内皮(ICE)综合征由于青光眼和/或角膜失代偿,有可能导致失明。基本病理似乎在于角膜内皮,许多研究证实,角膜内皮在裂隙灯检查时呈现出特征性的锤击银外观,在镜面显微镜下呈现图像反转。异常细胞的起源和形态尚不清楚。许多角膜移植术和小梁切除术标本的组织病理学研究揭示了多种细胞类型。本文报告了57例该综合征患者的一些大体和镜面显微镜数据,认为其他研究中组织病理学结果多样的原因是研究材料取样不佳,根据镜面显微镜标准推断异常细胞的形态,并将1例患者的镜面显微镜图像和扫描电子显微镜图像与其他报告中的图像进行比较。初步得出结论,异常细胞的外观是其三维形状的函数,并且它们会产生水泡样囊泡,这些囊泡会破裂、塌陷并最终内陷。