双侧巨大脉络膜溶洞1例：罕见的表现。

IF 0.9 4区医学 Q4 OPHTHALMOLOGY

Ophthalmic surgery, lasers & imaging retina Pub Date : 2025-04-01 Epub Date: 2025-02-01 DOI:10.3928/23258160-20241216-02

Rajul Shah, Udit Ajmani, Sameera Nayak, Niroj Kumar Sahoo, P Srinivas Rao, Brijesh Takkar

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引用次数: 0

摘要

本文报告一位22岁的女性，患有双侧巨大脉络膜空洞（CCs）的杆状锥体营养不良。她的最佳矫正视力为右眼20/80，左眼20/50。眼底检查显示视神经苍白，血管狭窄，弥漫性色素改变。眼底自身荧光显示中心区域的自身荧光减弱，周围有点点的自身荧光。视网膜电图显示暗位波和光位波振幅均下降，与杆状锥体营养不良（色素性视网膜炎）的诊断一致。光学相干断层扫描显示每只眼CC大，中央凹萎缩。巨大的CC伴着杆状锥体营养不良是一个显著的特征。[眼科外科激光成像视网膜2025；56: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。

查看原文本刊更多论文

Bilateral Giant Choroidal Cavern in a Case of Rod-Cone Dystrophy: A Rare Presentation.

This report presents a case of a 22-year-old woman with bilateral giant choroidal caverns (CCs) in rod-cone dystrophy. Her best-corrected visual acuity was 20/80 in the right eye and 20/50 in the left eye. Fundus examination showed optic nerve pallor, narrowed blood vessels, and diffuse pigmentary changes. Fundus autofluorescence showed a central area of reduced autofluorescence surrounded by stippled autofluorescence. An electroretinogram showed decreased amplitude of both scotopic and photopic waves, consistent with a diagnosis of rod-cone dystrophy (retinitis pigmentosa). Optical coherence tomography revealed large CC and foveal atrophy in each eye. A giant CC alongside rod-cone dystrophy is a distinctive feature. [Ophthalmic Surg Lasers Imaging Retina 2025;56:241-243.].

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来源期刊

Ophthalmic surgery, lasers & imaging retina OPHTHALMOLOGY-SURGERY

CiteScore

1.80

自引率

0.00%

发文量

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.