小儿单侧黄斑盘状病变的多模态成像。

Miriam Ehrenberg, Edward Barayev, Amit Meshi, Gad Dotan, Amir Sternfeld
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引用次数: 0

摘要

目的:报告连续6例儿科患者的临床表现、多模态影像学结果及电生理检查结果。所有患者无症状,有单侧、中央窝或中央窝周围病变。我们打算更好地定义和描述这一发现。方法:本回顾性病例系列在施耐德儿童医学中心进行。数据收集于2014年至2024年间,来自眼底检查中发现的圆形或椭圆形低色素单侧黄斑病变患者。这些患者随后接受视网膜成像和临床随访。对患者的临床、影像学及眼电生理资料进行分析。结果:6例患者被诊断为无症状,扁平,圆形或微卵圆形病变,边缘明确,通常位于中央窝或颞到中央窝。所有患者双眼视力均为20/20。病变大小约1.5椎间盘直径(DD),在红外(IR)成像中表现为高反射病变,在眼底自荧光成像中表现为高自荧光病变。通过病变的光学相干断层扫描(OCT)横截面显示视网膜外带+/-色素上皮(RPE)只有轻微的不规则性。多焦点ERG正常。在平均5.6年的随访期间,临床或影像学检查没有记录病变特征的变化。结论:本研究是迄今为止描述该实体的最大和最详细的研究。所有患者视力良好。在平均5.6年的随访期间,病变影像学特征未见进展。在完成测试的两名患者中,多焦点ERG结果正常。这些发现表明,至少在儿童时期,这是一个稳定的良性过程;因此,我们建议随访定期视网膜成像,并进一步研究,以可能确定这种实体的成人。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multi modal imaging of pediatric unilateral macular discoid lesions.

Purpose: To report the clinical findings, multimodal imaging results and electrophysiologic tests of 6 consecutive pediatric patients. All patients were asymptomatic and had a unilateral, foveal or peri-foveal lesion. We intent to better define and characterize this finding.

Methods: This retrospective case series was conducted at Schneider Children's Medical Center. Data gathered between 2014 and 2024, from patients with a round or oval hypopigmented unilateral macular lesion seen in fundus exam. These patients subsequently underwent retinal imaging and clinical follow-up. Clinical, imaging and ocular electrophysiologic data were analyzed for the patients.

Results: Six patients were diagnosed with an asymptomatic, flat, round or slightly oval lesion, with well-defined margins that was typically located in fovea or temporal to the fovea. Visual acuity was 20/20 in both eyes of all patients. The lesion's size was ~ 1.5 disc diameter (DD), it was easily noticed as a hyper-reflectant lesion in infra-red reflectance (IR) imaging and hyperautofluorescent in fundus autofluoresence imaging. Optical coherence tomography (OCT) cross section through the lesion showed only minimal irregularity in outer retinal bands +/- pigment epithelium (RPE). Multifocal ERG was normal. During an average follow up of 5.6 years, no change was documented clinically or per imaging studies in lesion characteristics.

Conclusions: This study is the largest and most detailed so far to describe this entity. All patients had excellent visual acuity. No progression was noted in lesion imaging characteristics during an average of 5.6 years follow up. Normal multifocal ERG results were achieved in the two patients who completed the test. These findings suggest a stationary benign course, at least in childhood; thus, we recommend follow up with periodic retinal imaging, and further research to possibly identify this entity in adults as well.

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