Suppr超能文献

虹膜劈裂症:一例病例报告及文献综述

Iridoschisis: a case report and literature review.

作者信息

Chen Yiyi, Qian Yiyong, Lu Peirong

机构信息

Department of Ophthalmology, The First Affiliated Hospital of Soochow University, 188 Shizi Street, Suzhou, 215006, People's Republic of China.

出版信息

BMC Ophthalmol. 2017 Mar 14;17(1):24. doi: 10.1186/s12886-017-0418-2.

Abstract

BACKGROUND

Iridoschisis is a rare condition that is characterized by the separation of the iris stroma into layers, with portions of the anterior layer floating freely in the aqueous humour. Here, we report three cases of iridoschisis that were complicated by either a cataract or glaucoma. Based on these cases, we speculate that the scope of iridoschisis has a rare association with intraocular pressure and the loss of corneal endothelial cells after surgery, which is mainly due to the surgery and not iridocorneal mechanical contact.

CASE PRESENTATION

We report three cases of iridoschisis, two of which were complicated by cataracts and the third by glaucoma. Patient 1 was a 69-year-old man with bilateral iridoschisis complicated by a cataract but not glaucoma, even though the entire anterior layer of the iris stroma in the right eye presented as white atrophic strands. To prevent the detached iris fibrils from invading the phacoemulsification tip and the irrigation/aspiration hand piece port, the separated iris stroma that was floating freely in the aqueous humour was cut with scissors immediately before the cataract extraction. Patient 2 was an 87-year-old woman with iridoschisis complicated by a cataract in the right eye. We successfully performed cataract surgery on the right eye without a pupillary device. Patient 3 was a 66-year-old man who presented with increased intraocular pressure with bilateral iridoschisis. He was discharged and prescribed with a combination of four glaucoma drugs.

CONCLUSIONS

Patients with iridoschisis should have continuous follow-up because complications may occur, and extra care from ophthalmologists is required.

摘要

背景

虹膜劈裂症是一种罕见病症,其特征为虹膜基质层分离,前层部分在房水中自由漂浮。在此,我们报告3例并发白内障或青光眼的虹膜劈裂症病例。基于这些病例,我们推测虹膜劈裂症范围与眼压及手术后角膜内皮细胞丢失存在罕见关联,这主要归因于手术而非虹膜角膜机械接触。

病例报告

我们报告3例虹膜劈裂症病例,其中2例并发白内障,第3例并发青光眼。病例1为一名69岁男性,双侧虹膜劈裂症并发白内障,但未并发青光眼,尽管右眼虹膜基质层的整个前层呈现为白色萎缩条索状。为防止分离的虹膜纤维侵入超声乳化针头及冲洗/抽吸手柄端口,在白内障摘除术前立即用剪刀剪去在房水中自由漂浮的分离虹膜基质。病例2为一名87岁女性,右眼虹膜劈裂症并发白内障。我们在未使用瞳孔装置的情况下成功为其右眼实施了白内障手术。病例3为一名66岁男性,双侧虹膜劈裂症伴眼压升高。他出院时被开具了四种青光眼药物的联合处方。

结论

虹膜劈裂症患者应持续接受随访,因为可能会出现并发症,并且需要眼科医生格外关注。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ce/5348740/7c0318f352f3/12886_2017_418_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验