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一名6个月大婴儿的黄斑部视网膜病变:早期临床及光学相干断层扫描结果

Torpedo Maculopathy in a 6-Month-Old Infant: Early Clinical and Optical Coherence Tomography Findings.

作者信息

Kara Caner, Petriçli İkbal Seza

出版信息

J Pediatr Ophthalmol Strabismus. 2017 Aug 24;54:e54-e57. doi: 10.3928/01913913-20170531-04.

DOI:10.3928/01913913-20170531-04
PMID:28837741
Abstract

A 6-month-old male infant presented for routine ophthalmologic examination. Indirect ophthalmoscopy revealed a flat, oval, hypopigmented lesion located in the temporal macula in the right eye with the tip pointing toward the fovea, which was compatible with torpedo maculopathy. Optical coherence tomography (OCT) was performed at the time of diagnosis. OCT scans of the lesion revealed slight retinal pigment epithelium hyperreflectivity. This case serves as the earliest OCT finding of the youngest patient diagnosed as having torpedo maculopathy in the literature. [J Pediatr Ophthalmol Strabismus. 2017;54:e54-e57.].

摘要

一名6个月大的男婴前来进行常规眼科检查。间接检眼镜检查发现右眼颞侧黄斑区有一个扁平、椭圆形、色素减退的病变,尖端指向中央凹,符合鱼雷状黄斑病变。诊断时进行了光学相干断层扫描(OCT)。病变的OCT扫描显示视网膜色素上皮有轻微的高反射性。该病例是文献中诊断为鱼雷状黄斑病变的最年轻患者最早的OCT检查结果。[《小儿眼科与斜视杂志》。2017年;54:e54 - e57。]

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引用本文的文献

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Long-term follow-up of torpedo maculopathy: a case series and mini-review.鱼雷样黄斑病变的长期随访:病例系列及小型综述。
BMC Ophthalmol. 2024 Jan 3;24(1):5. doi: 10.1186/s12886-023-03254-z.
2
Clinical evaluation of torpedo maculopathy in an infant population with additional genetic testing for NEXMIF mutation.对伴有 NEXMIF 突变基因检测的婴幼儿群体中 torpedo 斑的临床评估。
Eye (Lond). 2022 Aug;36(8):1639-1644. doi: 10.1038/s41433-021-01714-8. Epub 2021 Jul 29.
3
Distribution patterns of torpedo maculopathy: Further evidence of a congenital retinal nerve fiber layer-driven etiology.
鱼雷状黄斑病变的分布模式:先天性视网膜神经纤维层驱动病因的进一步证据。
Saudi J Ophthalmol. 2019 Jul-Sep;33(3):260-267. doi: 10.1016/j.sjopt.2019.07.010. Epub 2019 Aug 27.