Traumatic Lens Dislocation in an Eye with Anterior Megalophthalmos

IF 0.7 Q4 OPHTHALMOLOGY Case Reports in Ophthalmological Medicine Pub Date : 2022-05-09 DOI:10.1155/2022/6366949
Huda AlGhadeer
{"title":"Traumatic Lens Dislocation in an Eye with Anterior Megalophthalmos","authors":"Huda AlGhadeer","doi":"10.1155/2022/6366949","DOIUrl":null,"url":null,"abstract":"Anterior megalophthalmos is a rare, bilateral, nonprogressive, hereditary, congenital disorder characterized by the enlargement of all anterior segment structures of the eye, with megalocornea, iris atrophy, and zonular abnormalities. We report a case of an 8-year-old male who presented to the emergency department with a history of visual loss after a blunt ocular trauma to the left eye. The patient presented with markedly enlarged corneas and deepened anterior chambers bilaterally. Best-corrected visual acuity (BCVA) was hand motion in the left eye. An additional examination revealed multiple anterior segment abnormalities, leading to the diagnosis of megalophthalmos and lens dislocation in the anterior chamber. The patient underwent a lensectomy and anterior vitrectomy in the left eye. At six months postoperatively, the BCVA was 20/200 in the left eye. Lens dislocation in patients with megalocornea is rare. Cataract surgery in these patients requires attention to the zonular abnormalities and lens enlargement, resulting in increased rates of intraoperative and postoperative complications. Ophthalmologists should be able to diagnose this rare disorder and manage the associations and complications.","PeriodicalId":9603,"journal":{"name":"Case Reports in Ophthalmological Medicine","volume":"1 1","pages":""},"PeriodicalIF":0.7000,"publicationDate":"2022-05-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Case Reports in Ophthalmological Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2022/6366949","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"OPHTHALMOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Anterior megalophthalmos is a rare, bilateral, nonprogressive, hereditary, congenital disorder characterized by the enlargement of all anterior segment structures of the eye, with megalocornea, iris atrophy, and zonular abnormalities. We report a case of an 8-year-old male who presented to the emergency department with a history of visual loss after a blunt ocular trauma to the left eye. The patient presented with markedly enlarged corneas and deepened anterior chambers bilaterally. Best-corrected visual acuity (BCVA) was hand motion in the left eye. An additional examination revealed multiple anterior segment abnormalities, leading to the diagnosis of megalophthalmos and lens dislocation in the anterior chamber. The patient underwent a lensectomy and anterior vitrectomy in the left eye. At six months postoperatively, the BCVA was 20/200 in the left eye. Lens dislocation in patients with megalocornea is rare. Cataract surgery in these patients requires attention to the zonular abnormalities and lens enlargement, resulting in increased rates of intraoperative and postoperative complications. Ophthalmologists should be able to diagnose this rare disorder and manage the associations and complications.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
外伤性晶状体脱位伴前眼大症1例
前眼大症是一种罕见的双侧、非进行性、遗传性、先天性疾病,其特征是眼睛所有前节结构扩大,伴有大角膜、虹膜萎缩和带状异常。我们报告一个8岁的男性谁提出了一个钝性眼外伤后,左眼视力丧失的历史急诊科。患者表现为双侧角膜明显增大,前房加深。最佳矫正视力(BCVA)为左眼手部运动。另一项检查显示多发性前节异常,导致前房大眼和晶状体脱位的诊断。患者接受了左眼晶状体切除术和前玻璃体切除术。术后6个月,左眼BCVA为20/200。晶状体脱位在巨角膜患者中是罕见的。这些患者的白内障手术需要注意晶状体带异常和晶状体增大,导致术中和术后并发症的发生率增加。眼科医生应该能够诊断这种罕见的疾病和管理的关联和并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
38
审稿时长
14 weeks
期刊最新文献
Semaglutide Inducing Resolution of Proliferative Diabetic Retinopathy: A Case Report. Quantification of Goldmann Visual Fields During Resolution of Traumatic Optic Neuropathy. A Case of Pediatric Myopia Complicated by Vitreous Cyst: A Unique Ophthalmic Challenge. Optic Neuropathy AFG3L2 Related in a Patient Affected by Congenital Stationary Night Blindness. Sudden Visual Loss After Vitreoretinal Surgery: A Case Report.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1