Pre-Descemet's endothelial keratoplasty with glued intraocular lens implantation with pinhole pupilloplasty in a case of ocular comorbidity in achromatopsia.

IF 1 Q4 OPHTHALMOLOGY
Taiwan Journal of Ophthalmology Pub Date : 2024-03-15 eCollection Date: 2024-01-01 DOI:10.4103/tjo.TJO-D-23-00172
Dhivya Ashok Kumar, Amar Agarwal, Swetha Ravichandran
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引用次数: 0

Abstract

Ocular comorbidities can happen as congenital defective gene associations. We present a 37-year-old female patient who was mentally challenged and had coexisting achromatopsia gene abnormality on genetic analysis. She was operated in childhood for congenital cataract, and posterior chamber intraocular lens (IOL) was implanted at 10 years of age elsewhere. The patient presented 27 years later with luxated IOL with endothelial decompensation. There was a coexisting steep and thin cornea noted on corneal topography. She was managed with pre-Descemet's endothelial keratoplasty with transpositioning of posterior chamber IOL to glued IOL with single-pass four-throw pupilloplasty. Postoperatively, the cornea was clear with centered glued IOL. The lesser postanesthetic challenges and faster rehabilitation are obtained in combination procedures with reduced complications in such rare scenarios.

在一例无色素性视网膜病变患者的眼部合并症中,采用前去角皮内皮角膜移植术和针孔瞳孔成形术植入胶合型人工晶体。
眼部合并症可能与先天性缺陷基因有关。我们为您介绍一位 37 岁的女性患者,她有智力障碍,并且在基因分析中同时存在色弱基因异常。她在童年时因先天性白内障接受了手术,10 岁时在其他地方植入了后房型人工晶体(IOL)。27 年后,患者因内皮失代偿而出现人工晶体脱落。角膜地形图显示,患者的角膜陡薄。她接受了前戴斯麦内皮角膜移植术,将后房型人工晶体移位为粘连型人工晶体,并进行了单程四抛瞳孔成形术。术后,居中的胶合人工晶体使角膜变得清晰。在这种罕见的情况下,联合手术的麻醉后挑战较小,康复较快,并减少了并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.80
自引率
9.10%
发文量
68
审稿时长
19 weeks
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