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色素失禁症患者黄斑内层的结构异常

Structural Abnormalities of the Inner Macula in Incontinentia Pigmenti.

作者信息

Basilius Jacob, Young Marielle P, Michaelis Timothy C, Hobbs Ronald, Jenkins Glen, Hartnett M Elizabeth

机构信息

University of Utah School of Medicine, Salt Lake City.

Department of Ophthalmology and Visual Sciences, John A. Moran Eye Center, University of Utah, Salt Lake City.

出版信息

JAMA Ophthalmol. 2015 Sep;133(9):1067-72. doi: 10.1001/jamaophthalmol.2015.1700.

Abstract

IMPORTANCE

This report presents evidence from spectral-domain optical coherence tomography and fluorescein angiography of inner foveal structural abnormalities associated with vision loss in incontinentia pigmenti (IP).

OBSERVATIONS

Two children had reduced visual behavior in association with abnormalities of the inner foveal layers on spectral-domain optical coherence tomography. Fluorescein angiography showed filling defects in retinal and choroidal circulations and irregularities of the foveal avascular zones. The foveal to parafoveal ratios were greater than 0.57 in 6 eyes of 3 patients who had extraretinal neovascularization and/or peripheral avascular retina on fluorescein angiography and were treated with laser. Of these, 3 eyes of 2 patients had irregularities in foveal avascular zones and poor vision.

CONCLUSIONS AND RELEVANCE

Besides traction retinal detachment, vision loss in IP can occur with abnormalities of the inner foveal structure seen on spectral-domain optical coherence tomography, consistent with prior descriptions of foveal hypoplasia. The evolution of abnormalities in the neural and vascular retina suggests a vascular cause of the foveal structural changes. More study is needed to determine any potential benefit of the foveal to parafoveal ratio in children with IP. Even with marked foveal structural abnormalities, vision can be preserved in some patients with IP with vigilant surveillance in the early years of life.

摘要

重要性

本报告展示了来自光谱域光学相干断层扫描和荧光素血管造影的证据,证明色素失禁症(IP)中与视力丧失相关的中央凹内层结构异常。

观察结果

两名儿童在光谱域光学相干断层扫描中出现与中央凹内层异常相关的视觉行为减退。荧光素血管造影显示视网膜和脉络膜循环充盈缺损以及中央凹无血管区不规则。在荧光素血管造影显示有视网膜外新生血管形成和/或周边无血管视网膜并接受激光治疗的3例患者的6只眼中,中央凹与旁中央凹的比例大于0.57。其中,2例患者的3只眼中央凹无血管区不规则且视力差。

结论及相关性

除牵引性视网膜脱离外,IP患者的视力丧失可能与光谱域光学相干断层扫描所见的中央凹内层结构异常有关,这与先前关于中央凹发育不全的描述一致。神经视网膜和血管视网膜异常的演变提示中央凹结构变化的血管原因。需要更多研究来确定中央凹与旁中央凹比例对IP儿童的潜在益处。即使存在明显的中央凹结构异常,一些IP患者在生命早期进行密切监测仍可保留视力。

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