TOWARD AN IMAGING-CENTRIC DEFINITION OF NONPARANEOPLASTIC AUTOIMMUNE RETINOPATHY.

IF 2.3 2区 医学 Q2 OPHTHALMOLOGY
Lucy T Xu, Andrew Zheng, Jessica G Shantha, Steven Yeh, Jiong Yan, G Baker Hubbard, Purnima S Patel, Jonathan Waltuck, Ghazala O'Keefe, Nieraj Jain
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Abstract

Purpose: To explore characteristic imaging features of nonparaneoplastic autoimmune retinopathy (npAIR) to augment diagnostic criteria.

Methods: This is a retrospective cohort study of patients with npAIR evaluated at the Emory Eye Center between 2013 and 2019. Multimodal fundus images were evaluated to characterize the evolution of the disease.

Results: Twenty-one eyes of 12 patients were classified as having npAIR. Five patients (42%) were female, with median (range) age of 59 years (45-85 years). Median baseline visual acuity was 20/30 (20/20 to hand motions). Disease was asymmetric in 11 patients (92%). Common imaging findings included absence of bone spicules (86% of affected eyes), presence of attenuated vessels (86%), and speckled hypoautofluorescence in perimacular and perivenular regions. Three eyes were noted to present early with subtle splotchy fundus autofluorescence abnormality, ultimately developing characteristic speckled perimacular hypoautofluorescence. On optical coherence tomography, 18 eyes (86%) had loss of outer retinal bands with relative foveal sparing and a tapered transition zone.

Conclusion: Many eyes with npAIR exhibit a subacute, asymmetric, generalized photoreceptor degeneration featuring outer retinal atrophy with relative foveal sparing, retinal vascular attenuation, absence of bone spicules, and speckled hypoautofluorescence often in a perimacular and perivenular distribution. Findings of this study augment diagnostic criteria to improve specificity and accessibility of testing for npAIR.

为非副肿瘤性自身免疫性视网膜病变下一个以成像为中心的定义。
目的:我们探索了npAIR的特征性成像特征,以增强诊断标准:这是一项回顾性队列研究,研究对象是2013-2019年间在埃默里眼科中心接受评估的npAIR患者。对多模态眼底图像进行了评估,以描述疾病的演变特征:12名患者的21只眼睛被归类为npAIR。5名(42%)患者为女性,中位(范围)年龄为59岁(45-85岁)。基线视力中位数为 20/30(20/20 - HM)。11例(92%)患者的病情不对称。常见的影像学检查结果包括:无骨刺(86% 的患眼)、存在衰减的血管(86%)以及眼周和视网膜周围区域的斑点状低自荧光。有三只眼早期出现细微的斑点状 FAF 异常,最终发展为特征性的斑点状黄斑周围低自荧光。在 OCT 成像中,18 只眼睛(86%)的外层视网膜带缺失,眼窝相对稀疏,过渡区变细:结论:许多患有 npAIR 的眼球表现出亚急性、不对称的全身性感光细胞变性,其特点是视网膜外层萎缩,眼窝相对稀疏,视网膜血管衰减,骨刺缺失,斑点状低自荧光通常分布在视网膜周围和视网膜周围。我们的发现增强了诊断标准,提高了 npAIR 检测的特异性和可及性。
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
5.70
自引率
9.10%
发文量
554
审稿时长
3-6 weeks
期刊介绍: ​RETINA® focuses exclusively on the growing specialty of vitreoretinal disorders. The Journal provides current information on diagnostic and therapeutic techniques. Its highly specialized and informative, peer-reviewed articles are easily applicable to clinical practice. In addition to regular reports from clinical and basic science investigators, RETINA® publishes special features including periodic review articles on pertinent topics, special articles dealing with surgical and other therapeutic techniques, and abstract cards. Issues are abundantly illustrated in vivid full color. Published 12 times per year, RETINA® is truly a “must have” publication for anyone connected to this field.
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