Paul R H
Department of Ophthalmology, Duke University Medical Center, Durham, NC 27710.
Am J Ophthalmol. 1988 May 15;105(5):519-22. doi: 10.1016/0002-9394(88)90244-9.
I reviewed 20 previously published cases of presumed autoimmune corneal endotheliopathy. The disease appeared clinically with stromal edema and a slowly migrating line of keratic precipitates. All patients had acute stromal edema and keratic precipitates, and decreased visual acuity. Anterior chamber cells were noted in 11 patients. Inflammatory processes, such as pars planitis and iritis, and intraocular lens implantation were present in 13 patients.
我回顾了20例先前发表的疑似自身免疫性角膜内皮病变病例。该疾病在临床上表现为基质水肿和一条缓慢移动的角膜后沉着物带。所有患者均有急性基质水肿、角膜后沉着物和视力下降。11例患者有前房细胞。13例患者存在炎症过程，如周边葡萄膜炎和虹膜炎，以及人工晶状体植入。
