Idiopathic Photoreceptoritis: An Unusual Variant of Outer Retinopathy.

IF 2.6 4区 医学 Q2 OPHTHALMOLOGY
Ocular Immunology and Inflammation Pub Date : 2025-07-01 Epub Date: 2025-02-12 DOI:10.1080/09273948.2025.2461241
Yoo-Ri Chung, Adélaïde Toutée, Chérif Titah, Isabelle Audo, Michel Paques, Sarah Mrejen, Alain Gaudric, Bahram Bodaghi, Sara Touhami
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引用次数: 0

Abstract

Purpose: To report an unusual case of progressive photoreceptor disruption following a herpetic labial infection.

Method: Case report of a patient with severe idiopathic photoreceptoritis.

Results: A 46-year-old female patient presented with blurred vision and inferior photopsia in her right eye one week after a herpetic labial eruption. Initial examination revealed mild vitreous inflammation and focal photoreceptor alterations in the superior periphery of the right retina. Despite oral valaciclovir, the disease progressed rapidly, prompting referral to a tertiary care center. Autofluorescence and optical coherence tomography showed diffuse photoreceptor damage with impending foveal involvement. Extensive workup, including viral markers, was inconclusive. Given the temporal association with the herpetic infection and the sight-threatening progression, treatment was escalated to intravenous acyclovir and subsequently foscarnet for 2 weeks, which slowed down disease progression. The frontal margin of retinal foci stabilized with no further progression, while ellipsoid zone restoration was achieved following systemic corticosteroids and interferon alpha-2a.

Conclusion: The term "photoreceptoritis" describes conditions involving diffuse photoreceptor damage, predominantly unilateral, without primary choriocapillaritis. This case highlights a severe form of photoreceptoritis with diffuse photoreceptors loss, likely triggered by a herpetic labial infection. The disease was stabilized with antiviral therapy, while structural recovery of the photoreceptors was achieved through anti-inflammatory and immunosuppressive treatments. This report underscores the importance of a multidisciplinary approach to managing atypical retinal inflammatory disorders.

特发性光感受器炎:一种不同寻常的外视网膜病变。
目的:报告一个不寻常的情况下进行性光感受器破坏后疱疹性唇感染。方法:报告1例严重特发性光感受器炎患者。结果:一名46岁的女性患者在唇疱疹性唇疹后一周出现右眼视力模糊和下视性失光。初步检查显示轻度玻璃体炎症和右视网膜上周的局灶性光感受器改变。尽管口服了伐昔洛韦,但病情进展迅速,促使转诊到三级保健中心。自身荧光和光学相干断层扫描显示弥漫性光感受器损伤,伴有即将发生的中央凹受累。广泛的检查,包括病毒标记,没有定论。考虑到与疱疹感染和视力威胁进展的时间关联,治疗升级为静脉注射阿昔洛韦和随后的磷膦酸钠2周,这减缓了疾病进展。视网膜病灶额缘稳定,无进一步进展,而在全身皮质类固醇和干扰素α -2a治疗后,椭球区得以恢复。结论:术语“光感受器炎”描述的是弥漫性光感受器损伤,主要是单侧,无原发性绒毛膜毛细血管炎。这个病例强调了一种严重的光感受器炎,弥漫性光感受器丧失,可能由疱疹性唇感染引起。抗病毒治疗稳定了病情,而通过抗炎和免疫抑制治疗实现了光感受器的结构恢复。本报告强调了多学科方法管理非典型视网膜炎性疾病的重要性。
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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来源期刊
CiteScore
6.20
自引率
15.20%
发文量
285
审稿时长
6-12 weeks
期刊介绍: Ocular Immunology & Inflammation ranks 18 out of 59 in the Ophthalmology Category.Ocular Immunology and Inflammation is a peer-reviewed, scientific publication that welcomes the submission of original, previously unpublished manuscripts directed to ophthalmologists and vision scientists. Published bimonthly, the journal provides an international medium for basic and clinical research reports on the ocular inflammatory response and its control by the immune system. The journal publishes original research papers, case reports, reviews, letters to the editor, meeting abstracts, and invited editorials.
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