Brooks A M, West R H, Gillies W E
Glaucoma Investigation and Research Unit, Royal Victorian Eye and Ear Hospital, East Melbourne, Australia.
Ophthalmology. 1988 Sep;95(9):1234-43. doi: 10.1016/s0161-6420(88)33023-x.
Five patients are described with acute primary ischemic iris atrophy with almost complete loss of the normal radial vessels of the iris and fine microneovascularization. The atrophy of the iris was marked with a thin atrophic stroma, widely dilated pupil, and extensive loss of pigment from the posterior surface of the iris. The condition is of unknown etiology but occlusion of the greater vascular circle of the iris is possible. Iris angiography showed an almost total loss of the radial vessels of the iris with some patchy microneovascularization. In recent cases, the onset was acute and all patients had a raised intraocular pressure (IOP) except one who had already undergone a drainage operation. There was an accompanying low-grade uveitis or cyclitis in the chronic stage in all cases. The condition was unilateral and the posterior segment of the eye was normal so that good visual function was possible if the accompanying cataract and glaucoma were appropriately managed.
本文描述了5例急性原发性缺血性虹膜萎缩患者,其虹膜正常放射状血管几乎完全丧失,并伴有细微的微血管形成。虹膜萎缩表现为基质变薄、瞳孔广泛散大以及虹膜后表面色素大量脱失。该病病因不明,但虹膜大环阻塞有可能是其病因。虹膜血管造影显示虹膜放射状血管几乎完全丧失,伴有一些片状微血管形成。在近期病例中,起病急性,除1例已接受引流手术的患者外,所有患者眼压均升高。所有病例在慢性期均伴有轻度葡萄膜炎或睫状体炎。该病为单侧性,眼后段正常,因此如果能适当处理伴发的白内障和青光眼,有可能保持良好的视功能。