Ultrawidefield Fluorescein Angiography and OCT Findings in Children and Young Adults with Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy

IF 4.4 Q1 OPHTHALMOLOGY
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引用次数: 0

Abstract

Purpose

Autosomal dominant neovascular inflammatory vitreoretinopathy (ADNIV) is a rare genetic (CAPN5) autoimmune condition typically diagnosed in adulthood and characterized by a triad of inflammation, retinal degeneration, and neovascularization. We report novel multimodal imaging findings in children and young adults with ADNIV, and early treatment response to short-duration local and systemic corticosteroids.

Design

Retrospective consecutive case series.

Participants

Ten patients aged <25 years with ADNIV and available multimodal imaging.

Methods

The medical records of patients aged <25 years with a diagnosis of ADNIV with ultrawidefield fluorescein angiography (UWFFA) and OCT data were reviewed.

Main Outcome Measures

Ultrawidefield fluorescein angiography and OCT findings at baseline and after local corticosteroids.

Results

Median age at presentation was 14 years (range, 9–24 years). OCT on presentation demonstrated cystoid macular edema in 8 of 20 eyes and symptomatic vitreoretinal interface disease in 2 of 20 eyes. Initial UWFFA demonstrated retinal vascular leakage (20/20 eyes, 100%), peripheral nonperfusion (13/20 eyes, 65%), and retinal neovascularization (6/20 eyes, 30%). Retinal vascular leakage improved with local corticosteroids, and neovascularization regressed with anti-VEGF therapy.

Conclusions

Ultrawidefield fluorescein angiography findings of prefibrotic ADNIV reported in adults were also present in children and young adults. Early testing for a pathogenic CAPN5 variant in at-risk children and regularly scheduled screening for uveitis and retinal vasculitis with UWFFA and OCT may prompt earlier intervention. Short-duration local steroids are effective at treating retinal vascular leakage and macular edema but are not durable, suggesting a potential role for steroid-sparing immunosuppressive therapy. Early treatment may alter the natural history of disease.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
常染色体显性新生血管炎症性玻璃体视网膜病变 (ADNIV) 儿童和青少年的超宽视场荧光素血管造影和光学视网膜断层扫描结果。
目的:常染色体显性新生血管炎性玻璃体视网膜病变(ADNIV)是一种罕见的遗传性(CAPN5)自身免疫性疾病,通常在成年后诊断,其特征是炎症、视网膜变性和新生血管三联征。我们报告了患有 ADNIV 的儿童和年轻成人的新型多模态成像结果,以及对短期局部和/或全身皮质类固醇的早期治疗反应:设计:回顾性连续病例系列:方法:收集25岁以下ADNIV患者的医疗记录:方法:回顾25岁以下诊断为ADNIV的患者的医疗记录,包括超宽场荧光素血管造影(UWFFA)和光学相干断层扫描(OCT)数据:主要结果指标:基线和局部皮质类固醇治疗后的超宽视野荧光素血管造影(UWFFA)和光学相干断层扫描(OCT)结果:中位发病年龄为14岁(9-24岁)。8/20眼的OCT显示有CME,2/20眼有症状性玻璃体视网膜界面病变。最初的 UWFFA 显示视网膜血管渗漏(20/20 眼,100%)、周边无灌注(13/20 眼,65%)和视网膜新生血管(6/20 眼,30%)。局部皮质类固醇治疗可改善视网膜血管渗漏,抗血管内皮生长因子治疗可使新生血管消退:结论:UWFFA 在成人中发现的 ADNIV 前纤维化现象在儿童和青少年中也同样存在。对高危儿童进行早期CAPN5致病变体检测,并定期用UWFFA和OCT筛查葡萄膜炎和视网膜血管炎,可促使早期干预。短效局部类固醇可有效治疗视网膜血管渗漏和黄斑水肿,但疗效不持久,这表明类固醇替代免疫抑制疗法具有潜在作用。早期治疗可能会改变疾病的自然病史。
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来源期刊
Ophthalmology. Retina
Ophthalmology. Retina Medicine-Ophthalmology
CiteScore
7.80
自引率
6.70%
发文量
274
审稿时长
33 days
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