特发性中枢性浆液性脉络膜视网膜病变无激光长期随访。

D. Bujarborua
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引用次数: 94

摘要

目的观察未经激光治疗的特发性中枢性浆液性脉络膜视网膜病变(ICSC)患者的不同类型眼底表现,并对这些病例进行7 ~ 23年的长期随访,评估其最终视力结果。方法本研究选取了5例ICSC病例,这些病例较好地代表了该疾病在眼底的不同晚期表现。我们审查了我院的病例记录,以及其他地方以前的治疗记录。在最后评估当天,每个病例重复进行完整的眼科检查、常规实验室检查和荧光素眼底血管造影(FFA)。结果本组病例均可见与老年性黄斑变性(AMD)相似的黄斑区色素紊乱、广泛的视网膜色素上皮(RPE)萎缩及黄斑出血。结论sicsc的病程不可预测,没有明确的临床线索预测其最终结局。在相当长的一段时间内,这种情况有可能复发。
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Long-term follow-up of idiopathic central serous chorioretinopathy without laser.
PURPOSE The purpose of this study was to observe the varied types of manifestations in the fundus of patients with idiopathic central serous chorioretinopathy (ICSC) without laser treatment and also to assess the ultimate visual outcome in such cases in a long-term follow-up ranging from 7 to 23 years. METHODS This study is confined to 5 selected cases of ICSC which fairly represent the different types of late stage manifestations of the disease in the fundus. Case records from our hospital, as well as available records of previous treatment elsewhere were reviewed. A complete ophthalmological examination, routine laboratory investigations and fluorescein fundus angiography (FFA) were repeated in each case on the day of final evaluation. RESULTS Pigmentary disturbances in the macular area resembling to some extent age-related macular degeneration (AMD), extensive retinal pigment epithelial (RPE) atrophy and macular haemorrhage have been observed in the fundus of the reviewed cases. CONCLUSIONS ICSC runs an unpredictable course and there are no definitive clinical clues to predict its ultimate outcome. Recurrence of the condition is a possibility for a considerable period of time.
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Reply: Acta Ophthalmologica Scandinavica 2005 Ocular malformations with embryonic implications C. R. Cavonius: Color Vision Deficiencies XIII In Honour of SVEN ERIK NILSSON Ophthalmological aspects of prematurity
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