Abbott R L, Fine B S, Webster R G, Paglen P G, Spencer W H
Ophthalmology. 1981 Aug;88(8):788-800. doi: 10.1016/s0161-6420(81)34959-8.
Six phakic patients with unilateral corneal edema and clinically normal-appearing fellow eyes were examined with specular microscopy and found to have endothelial pleomorphism and reduced cell counts in the nonedematous cornea. None of these patients had any previous eye disease, trauma, inflammation, or surgery. Clinically unrecognized endothelial disease was proposed as a cause for the unilateral corneal edema and was verified by light and electron microscopic studies in five patients. These pathologic findings vary somewhat from those found in Fuchs' dystrophy and may represent either a variant or a form of endothelial cell degeneration of as yet undetermined etiology. Our studies suggest that this condition is not detectable in the nonedematous cornea by standard high magnification biomicroscopy and requires the use of the clinical specular microscope to confirm the diagnosis in suspected cases.
对6例患有单侧角膜水肿且健侧眼外观正常的有晶状体眼患者进行了镜面显微镜检查,发现非水肿角膜存在内皮多形性且细胞计数减少。这些患者均无既往眼部疾病、外伤、炎症或手术史。临床上未被识别的内皮疾病被认为是单侧角膜水肿的病因,并在5例患者中通过光镜和电镜研究得到证实。这些病理表现与富克斯营养不良有所不同,可能代表一种尚未明确病因的内皮细胞变性的变异型或形式。我们的研究表明,这种情况在非水肿角膜中通过标准高倍生物显微镜无法检测到,疑似病例需要使用临床镜面显微镜来确诊。