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急性双侧视网膜和脉络膜脱离——病例报告

Acute bilateral retinal and choroidal detachment - A case report.

作者信息

Vienne-Jumeau Aliénor, Toutée Adélaïde, Zegrari Samira, Jamart Céline, Audo Isabelle, Paques Michel, Mrejen Sarah

机构信息

Centre hospitalier national d'ophtalmologie des Quinze-Vingts, Paris, France.

Borelli Centre, UMR 9010, CNRS-SSA-ENS Paris Saclay-Université Paris Cité, 91190 Paris, France.

出版信息

Retin Cases Brief Rep. 2025 Jul 22. doi: 10.1097/ICB.0000000000001793.

Abstract

PURPOSE

To report an unusual episode of acute bilateral retinal and choroidal detachment.

METHODS

Case report.

RESULTS

We report the case of a fifty-seven-year-old male referred to the emergency department for an acute bilateral retinal detachment. He had experienced profound visual loss three weeks earlier while hospitalized for sepsis of unknown cause. Fundoscopy revealed bilateral annular retinal and choroidal detachment, confirmed by echography. An extensive work-up was negative, and the patient was given steroid boluses for suspected uveal effusion syndrome, although the axial length was normal. After five days of steroid treatment, minimal improvement was observed. The treatment was discontinued, and new multimodal imaging revealed a hyperfluorescent spot on fluorescein angiography (FA) in the right eye with subretinal hyperreflective material on corresponding optical coherence tomography suggesting fibrin and adjacent serous detachment. The spot was treated with laser photocoagulation, and the retinal detachment started to decrease two days later. Additional hyperfluorescent spots were later found and treated with laser photocoagulation. Over a few weeks, both functional and anatomical improvements were observed. Over the course of seven months, the central serous retinal detachment slowly and completely resolved while vision progressively and dramatically improved. This very slow and dramatic anatomical and functional improvement was atypical for both uveal effusion syndrome and central serous chorioretinopathy.

CONCLUSIONS

This atypical case of type-3 uveal effusion syndrome presented as acute bilateral retinal and choroidal detachment with central serous chorioretinopathy-like features. Multifocal laser photocoagulation may have improved both functional and anatomical outcomes, with dramatic recovery after seven months.

摘要

目的

报告一例罕见的急性双侧视网膜和脉络膜脱离病例。

方法

病例报告。

结果

我们报告了一名57岁男性因急性双侧视网膜脱离被转诊至急诊科的病例。三周前,他因不明原因的脓毒症住院期间出现了严重的视力丧失。眼底检查发现双侧环形视网膜和脉络膜脱离,经超声检查确诊。全面检查结果为阴性,尽管眼轴长度正常,但鉴于怀疑为葡萄膜渗漏综合征,患者接受了大剂量类固醇治疗。类固醇治疗五天后,仅观察到轻微改善。治疗中断,新的多模式成像显示右眼荧光素血管造影(FA)上有一个高荧光点,相应的光学相干断层扫描显示视网膜下有高反射物质,提示为纤维蛋白及相邻的浆液性脱离。该点接受了激光光凝治疗,两天后视网膜脱离开始减轻。随后又发现了其他高荧光点并进行了激光光凝治疗。几周内,观察到了功能和解剖学上的改善。在七个月的时间里,中心性浆液性视网膜脱离缓慢且完全消退,同时视力逐渐显著改善。这种非常缓慢且显著的解剖学和功能改善对于葡萄膜渗漏综合征和中心性浆液性脉络膜视网膜病变来说都是非典型的。

结论

这例非典型的3型葡萄膜渗漏综合征表现为急性双侧视网膜和脉络膜脱离,并伴有中心性浆液性脉络膜视网膜病变样特征。多焦点激光光凝可能改善了功能和解剖学结果,七个月后视力显著恢复。

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