中枢性浆液性脉络膜视网膜病变:发病机制、危险因素、诊断方法和目前治疗的综述

A. K. Kocak altintas
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引用次数: 0

摘要

中枢性浆液性脉络膜视网膜病变(CSCR)以黄斑处神经感觉层浆液性脱离为特征。复发率较高,以中年男性为主。该病的病因和发病机制仍不清楚。而脉络膜改变增加脉络膜血管通透性是CSCR的基本病理。FAF、FFA、OCT、OCTA、ICG等不同的诊断方法可检测其脉络膜厚度、脉络膜血管指数、高反射点等生物标志物,准确诊断和治疗效果。急性CSCR通常是自限性的,但在复发或慢性形式中,由于视网膜色素上皮萎缩的感光层进行性和不可逆损伤,可能导致永久性视力丧失。已经报道了几种治疗方案,如PDT,玻璃体内抗vegf, TTT,激光,矿皮质激素受体拮抗剂治疗慢性和复发性CSCR。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Central Serous Chorioretinopathy: A Review of Pathogenesis, Risk Factors, Diagnostic Methods and the Current Treatments
Central serous chorioretinopathy (CSCR) is characterized by serous detachment of the neurosensory layer at the macula. It has a relatively high recurrence rate and mainly affecting middle-aged males. The etiology and pathogenesis of the disease still remain ambiguous. But choroidal changes which increase choroidal vascular permeability are the basic pathology of CSCR. Different diagnostic methods such as FAF, FFA, OCT, OCTA, ICG could be used to detect its biomarkers such as choroidal thickness, choroidal vascularity index, hyperreflective dots for exact diagnosis and treatment response. Acute CSCR generally self-limited, but in recurrent or chronic forms may cause permanent visual loss due to progressive and irreversible damage in the photoreceptor layer of retinal pigment epithelium atrophy. Several treatment alternatives have been reported, such as PDT, intravitreal Anti-VEGF, TTT, Laser, Mineralocorticoid receptor antagonist for chronic and recurrent CSCR.
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