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免疫功能正常宿主中的 EBV 急性视网膜坏死。

EPSTEIN-BARR VIRUS ACUTE RETINAL NECROSIS IN AN IMMUNOCOMPETENT HOST.

机构信息

Department of Ophthalmology, Jewish General Hospital, Montreal, Quebec, Canada.

Montreal Retina Institute, Montreal, Quebec, Canada ; and.

出版信息

Retin Cases Brief Rep. 2021 Jul 1;15(4):412-416. doi: 10.1097/ICB.0000000000000819.

Abstract

PURPOSE

To describe a case of Epstein-Barr virus (EBV)-associated acute retinal necrosis (ARN) in an immunocompetent patient and to summarize the clinical features of published molecularly confirmed EBV-ARN cases.

METHODS

Case report and literature review.

RESULTS

An 83-year-old immunocompetent woman with unilateral ARN presented with visual acuity of light perception. Oral valacyclovir was started. One week later, vitrectomy was conducted for worsening inflammation. Intraoperatively, a severe confluent necrotizing retinitis and occlusive vasculitis involving all four quadrants of posterior and peripheral retina were noted. Vitreous polymerase chain reaction was exclusively positive for EBV. Other autoimmune, infective, and hematological work-up was negative. The retinitis resolved 3 months later, but with significant macular and generalized retinal atrophy, visual acuity remained light perception. From the literature, there are four EBV-ARN cases (six eyes) diagnosed based on polymerase chain reaction or fluorescence in-situ hybridization of vitreous or retinal samples. All patients were immunocompromised or on immunosuppressive treatment. Presenting visual acuity was light perception or worse in 3/6 eyes. Three patients received systemic acyclovir-based therapy. Vitrectomy was performed in 4/6 eyes between 4 and 8 weeks from disease onset. All cases had involvement of the posterior and peripheral retina. Retinal detachment occurred in 2/6 eyes, and final visual acuity was no light perception in 3/6 eyes.

CONCLUSION

This case expands the clinical spectrum of EBV-ARN to include infection in immunocompetent hosts. Epstein-Barr virus-ARN seems to be characterized by a global peripheral and posterior fulminant retinitis, with adverse visual acuity outcomes despite systemic acyclovir-based therapy. The benefits of adjunctive intravitreal foscarnet, systemic steroids, and early vitrectomy may warrant further investigation.

摘要

目的

描述一例免疫功能正常的患者中由 EBV 引起的急性视网膜坏死(ARN),并总结已发表的经分子确证的 EBV-ARN 病例的临床特征。

方法

病例报告和文献复习。

结果

一名 83 岁免疫功能正常的女性单侧 ARN 患者,视力为光感。开始口服伐昔洛韦。一周后,炎症恶化时行玻璃体切除术。术中发现严重融合性坏死性视网膜炎和闭塞性血管炎,累及后极和周边视网膜的所有四个象限。玻璃体聚合酶链反应仅 EBV 呈阳性。其他自身免疫、感染和血液学检查均为阴性。3 个月后,视网膜炎消退,但黄斑和广泛性视网膜萎缩明显,视力仍为光感。从文献中,有 4 例 EBV-ARN 病例(6 只眼)根据玻璃体或视网膜样本的聚合酶链反应或荧光原位杂交诊断。所有患者均免疫功能低下或正在接受免疫抑制治疗。6 只眼中 3 只眼的初始视力为光感或更差。3 例患者接受了全身性阿昔洛韦治疗。4 例患者在发病后 4 至 8 周行玻璃体切除术。所有病例均累及后极和周边视网膜。2 例患者发生视网膜脱离,6 只眼中 3 只眼的最终视力无光感。

结论

该病例将 EBV-ARN 的临床表现扩展到包括免疫功能正常的宿主感染。EBV-ARN 似乎表现为全身性周边和后部暴发性视网膜炎,尽管进行了全身性阿昔洛韦治疗,但视力预后仍不佳。辅助玻璃体内膦甲酸、全身皮质类固醇和早期玻璃体切除术的益处可能需要进一步研究。

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