中枢性浆液性脉络膜视网膜病变:多模式成像和管理选择。

IF 0.7 Q4 OPHTHALMOLOGY Case Reports in Ophthalmological Medicine Pub Date : 2020-08-14 eCollection Date: 2020-01-01 DOI:10.1155/2020/8890404
Prashanth G Iyer, Stephen G Schwartz, Jonathan F Russell, Harry W Flynn
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引用次数: 6

摘要

中枢性浆液性脉络膜视网膜病变(CSCR)是一种特发性黄斑病变,其特征是脉络膜增厚、视网膜色素上皮脱离和可变视网膜下液。CSCR主要影响年轻男性,其危险因素包括皮质类固醇的使用、A型行为模式和心理压力。虽然通常自限性和良好的视力预后,复发性和持续性CSCR可导致视网膜外和/或视网膜色素上皮萎缩,脉络膜新生血管和视力丧失。本文回顾了目前的多模式成像和治疗方案,包括观察、矿皮质激素受体拮抗剂、热激光光凝和使用维替波芬的超说明书光动力治疗。
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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Central Serous Chorioretinopathy: Multimodal Imaging and Management Options.

Central serous chorioretinopathy (CSCR) is an idiopathic maculopathy characterized by thickened choroid, retinal pigment epithelial detachment, and variable subretinal fluid. CSCR predominantly affects young men, with risk factors including corticosteroid use, the type A behavior pattern, and psychological stress. While usually self-limited with a good visual prognosis, recurrent and persistent CSCR can lead to outer retinal and/or retinal pigment epithelial atrophy, choroidal neovascularization, and visual loss. This article reviews current multimodal imaging and treatment options, which include observation, mineralocorticoid receptor antagonists, thermal laser photocoagulation, and off-label photodynamic therapy with verteporfin.

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审稿时长
14 weeks
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