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多模态成像在凸出于神经视网膜表面的睫状视网膜毛细血管血管瘤诊断中的应用。

Multimodal Imaging in the Diagnosis of Exophytic Juxtapapillary Retinal Capillary Hemangioblastoma.

机构信息

Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, Florida, USA.

The Baylor College of Medicine, Houston, Texas, USA.

出版信息

Am J Ophthalmol. 2021 May;225:128-136. doi: 10.1016/j.ajo.2021.01.002. Epub 2021 Jan 12.

Abstract

PURPOSE

Exophytic juxtapapillary retinal capillary hemangioblastoma (JRCH) can be difficult to diagnose. We explore the value of multimodal imaging to aid in the diagnosis.

DESIGN

Retrospective case series.

METHODS

Medical records and multimodal imaging studies were reviewed on all patients diagnosed with RCH at Bascom Palmer Eye Institute, Miami, Florida, between January 2013 and December 2019. Patients with exophytic lesions within 2 mm of the disc were included. One patient from the Baylor College of Medicine, Houston, Texas was included. Patient demographics, referring diagnosis, history of von Hippel-Lindau syndrome, initial and last visual acuity, and treatments were recorded. Fundus photography, fundus autofluorescence, fluorescein angiography, indocyanine green angiography, optical coherence tomography (OCT), OCT angiography, and B-scan images were reviewed.

RESULTS

Twelve patients were identified with exophytic JRCH. The mean age was 54 years (range 38-73 years). Five patients had von Hippel-Lindau syndrome. The most common referral diagnoses were choroidal neovascularization and neuroretinitis. Imaging features included nodular outer retinal thickening with shadowing and intra-/subretinal fluid on OCT, hypoautofluorescence on fundus autofluorescence, middle to outer retinal hypervascularity on OCT angiography, early hyperfluorescence with late leakage on fluorescein angiography, and lack of choroidal vascular lesion on indocyanine green angiography. Treatments included photodynamic therapy (6 patients), intravitreal anti-vascular endothelial growth factor therapy (6 patients), argon laser photocoagulation (2 patients), intravitreal or sub-Tenon's triamcinolone (3 patients), and observation (4 patients).

CONCLUSIONS

A key to the accurate diagnosis of exophytic JRCH is its intraretinal location, typically involving the outer retinal layers, which results in a clinical appearance that is distinct from the more common and easily recognizable endophytic RCH. Multimodal imaging can aid in ruling out choroidal neovascularization and disc edema by demonstrating an absence of involvement of those structures.

摘要

目的

外生型 juxtapapillary 视网膜毛细血管血管瘤(JRCH)的诊断可能较为困难。我们旨在探讨多模态成像在辅助诊断中的作用。

设计

回顾性病例系列。

方法

回顾性分析 2013 年 1 月至 2019 年 12 月期间在佛罗里达州迈阿密的 Bascom Palmer 眼科研究所诊断为 RCH 的所有患者的病历和多模态成像研究资料。纳入距盘状结构 2mm 以内有外生病变的患者。纳入一名来自德克萨斯州休斯顿贝勒医学院的患者。记录患者的人口统计学特征、转诊诊断、von Hippel-Lindau 综合征病史、初始和最后视力以及治疗情况。评估眼底照相、眼底自发荧光、荧光素血管造影、吲哚菁绿血管造影、光学相干断层扫描(OCT)、OCT 血管造影和 B 型超声图像。

结果

共确定了 12 例外生型 JRCH 患者。平均年龄为 54 岁(范围 38-73 岁)。5 例患者患有 von Hippel-Lindau 综合征。最常见的转诊诊断是脉络膜新生血管和神经视网膜炎。影像学特征包括 OCT 上见结节状外层视网膜增厚伴遮蔽,伴或不伴视网膜下积液;眼底自发荧光呈低自发荧光;OCT 血管造影上见中-外层视网膜高血管化;荧光素血管造影上见早期强荧光伴晚期渗漏;吲哚菁绿血管造影上未见脉络膜血管病变。治疗方法包括光动力疗法(6 例)、抗血管内皮生长因子玻璃体腔注射(6 例)、氩激光光凝(2 例)、玻璃体内或经 Tenon 囊曲安奈德注射(3 例)和观察(4 例)。

结论

准确诊断外生型 JRCH 的关键是其位于视网膜内,通常累及外层视网膜,这导致其临床表现与更为常见且易于识别的内生型 RCH 明显不同。多模态成像可以通过显示这些结构无受累来帮助排除脉络膜新生血管和盘状水肿。

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