Central serous chorioretinopathy: Recent trends

Abhishek Das, P. Chheda
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Abstract

Central serous chorioretinopathy (CSCR) belongs to pachychoroid spectrum of diseases, and the pathogenesis is still not fully understood. It is associated with multiple systemic factors. It is characterized by the collection of fluid between the retinal pigment epithelium (RPE) and the neurosensory retina. It mostly affects young men under perceived stress. The involvement of corticosteroids is undisputed although their exact role has not been clarified; other parts of the underlying mechanism of CSCR have been mainly elucidated by imaging techniques, such as fluorescein and indocyanine green angiography. The course is usually self-limiting and in most cases resolves spontaneously within a 3–6-month period, with visual acuity usually recovering to 20/30 or better. However, chronic CSC may develop as a consequence of recurrences or persistent neurosensory detachment and can result in progressive RPE atrophy and permanent visual loss. We used search terms such as “central serous retinopathy,” “central serous chorioretinopathy,” “CSCR,” “management,” and “treatment” and also the keywords of each type of treatment on PubMed and Medline to retrieve articles for this systematic review.
中心性浆液性脉络膜视网膜病变:近期趋势
中枢性浆液性脉络膜视网膜病变(CSCR)属于厚脉络膜谱系疾病,其发病机制尚不完全清楚。它与多种系统因素有关。它的特征是视网膜色素上皮(RPE)和神经感觉视网膜之间的液体聚集。它主要影响处于感知压力下的年轻男性。皮质类固醇的参与是无可争议的,尽管它们的确切作用尚未明确;其他部分CSCR的潜在机制主要通过成像技术,如荧光素和吲哚菁绿血管造影来阐明。这个过程通常是自限性的,大多数情况下在3 - 6个月的时间内自然消退,视力通常恢复到20/30或更好。然而,慢性CSC可作为复发或持续性神经感觉脱离的结果发展,并可导致进行性RPE萎缩和永久性视力丧失。我们使用诸如“中枢浆液性视网膜病变”、“中枢浆液性脉络膜视网膜病变”、“CSCR”、“管理”和“治疗”等搜索词以及PubMed和Medline上每种治疗类型的关键词来检索本系统综述的文章。
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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