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儿童单侧黄斑盘状病变的多模态成像

Multi modal imaging of pediatric unilateral macular discoid lesions.

作者信息

Ehrenberg Miriam, Barayev Edward, Meshi Amit, Dotan Gad, Sternfeld Amir

机构信息

Department of Ophthalmology, Ophthalmology Unit, Schneider Children's Medical Center in Israel, 14 Kaplan Street, Petach Tikva, Israel.

Gray Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

出版信息

Graefes Arch Clin Exp Ophthalmol. 2025 Jun 27. doi: 10.1007/s00417-025-06873-y.

Abstract

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.

摘要

目的

报告6例连续儿科患者的临床检查结果、多模态成像结果及电生理检查情况。所有患者均无症状,且有单侧、黄斑中心凹或中心凹周围病变。我们旨在更好地界定和描述这一发现。

方法

本回顾性病例系列研究在施耐德儿童医学中心开展。收集2014年至2024年期间眼底检查发现有单侧圆形或椭圆形色素减退性黄斑病变患者的数据。这些患者随后接受了视网膜成像及临床随访。对患者的临床、成像及眼电生理数据进行分析。

结果

6例患者被诊断为无症状的扁平圆形或略呈椭圆形病变,边界清晰,通常位于黄斑中心凹或中心凹颞侧。所有患者双眼视力均为20/20。病变大小约为1.5视盘直径(DD),在红外反射(IR)成像中很容易被视为高反射性病变,在眼底自发荧光成像中呈高自发荧光。通过病变的光学相干断层扫描(OCT)横断面显示视网膜外层带和/或色素上皮(RPE)仅有轻微不规则。多焦视网膜电图正常。在平均5.6年的随访期间,病变特征在临床或成像研究中均无变化。

结论

本研究是迄今为止描述该疾病实体规模最大、最详细的研究。所有患者视力均极佳。在平均5.6年的随访期间,病变成像特征未见进展。完成检查的2例患者多焦视网膜电图结果正常。这些发现提示至少在儿童期病程呈静止良性;因此,我们建议定期进行视网膜成像随访,并进一步开展研究,以便在成人中也可能识别出该疾病实体。

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