阿尔波特综合征黄斑孔修补术后视网膜脱离。

IF 0.9 4区 医学 Q4 OPHTHALMOLOGY
Brian Chhoy, Karen M Wai, Theodore Leng
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引用次数: 0

摘要

阿尔波特综合征的特征是 IV 型胶原蛋白网络中断,导致肾脏、听觉和眼部表现。本病例报告详细描述了一名 24 岁的 Alport 综合征患者在黄斑孔修补术后发生流变性视网膜脱离的情况。该患者成功接受了玻璃体切除术和黄斑孔修补术内缘膜剥离术,但在五周之后又因视网膜脱离而导致视力下降,因此必须进行巩膜扣带和玻璃体切除术。这是第一例描述 Alport 综合征黄斑孔修补术后流变性视网膜脱离的病例。[眼科手术激光成像视网膜2024;55:XX-XX]。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Retinal Detachment After Macular Hole Repair in Alport Syndrome.

Alport syndrome is characterized by type IV collagen network disruptions leading to renal, auditory, and ocular manifestations. This case report details a 24-year-old man with Alport syndrome who developed a rhegmatogenous retinal detachment following macular hole repair. The patient underwent a successful vitrectomy and internal limiting membrane peel for macular hole repair but returned with vision loss due to retinal detachment five weeks later, which necessitated a combined scleral buckle and vitrectomy. This is the first case describing rhegmatogenous retinal detachment post-macular hole repair in Alport syndrome. [Ophthalmic Surg Lasers Imaging Retina 2024;55:289-292.].

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来源期刊
CiteScore
1.80
自引率
0.00%
发文量
89
期刊介绍: OSLI Retina focuses exclusively on retinal diseases, surgery and pharmacotherapy. OSLI Retina will offer an expedited submission to publication effort of peer-reviewed clinical science and case report articles. The front of the journal offers practical clinical and practice management features and columns specific to retina specialists. In sum, readers will find important peer-reviewed retina articles and the latest findings in techniques and science, as well as informative business and practice management features in one journal.
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