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一例伴有小角膜综合征的缺损性大眼球中的视网膜脱离病例。

A case of retinal detachment in colobomatous macrophthalmos with microcornea syndrome.

作者信息

Seung Hyun Kyung, Kim Ha Kyoung, Nam Woo Ho

机构信息

Hanil General Hospital, Seoul, Korea.

出版信息

Korean J Ophthalmol. 2009 Dec;23(4):312-4. doi: 10.3341/kjo.2009.23.4.312. Epub 2009 Dec 4.

Abstract

We report a rare case of retinal detachment in colobomatous macrophthalmos with microcornea syndrome. A 25-year-old female who had suffered from poor vision in her left eye since early childhood and high myopia in her right eye (-11 D) visited our clinic because of a sudden deterioration of vision. Examination of the anterior segment showed microcornea with coloboma of the inferior pupil margin in the left iris. Fundus examination of the left eye revealed an inferior choroidal coloboma extending from the optic disc and macula. The patient also had total bullous retinal detachment. Pars plana vitrectomy with silicone oil tamponade was performed, and the retina was reattached. In the very rare condition of colobomatous macropthalmos with microcornea, retinal detachment may develop. Pars plana vitrectomy with additional silicone oil tamponade may be performed to treat this condition.

摘要

我们报告了一例患有无虹膜脉络膜缺损性大眼球合并小角膜综合征的视网膜脱离罕见病例。一名25岁女性自幼左眼视力不佳,右眼高度近视(-11 D),因视力突然恶化前来我院就诊。眼前节检查显示左眼虹膜下方瞳孔缘有小角膜及缺损。左眼眼底检查发现从视盘和黄斑延伸的下方脉络膜缺损。患者还患有全泡状视网膜脱离。行玻璃体切除术联合硅油填充,视网膜复位。在无虹膜脉络膜缺损性大眼球合并小角膜这种极为罕见的情况下,可能会发生视网膜脱离。可通过行玻璃体切除术并额外进行硅油填充来治疗这种情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e4c/2789960/eeaabccf9fe2/kjo-23-312-g001.jpg

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