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自适应光学检眼镜、多焦视网膜电图和光学相干断层扫描血管造影在疑似鱼雷样黄斑病变伴卵黄样病变的独特病例中的应用

Adaptive optics ophthalmoscopy, multifocal ERG and OCTA in unique case of suspected torpedo maculopathy presenting with vitelliform lesion.

作者信息

Lambert Nathan G, Grigorian Florin, Vasconcelos Huber, Watzke Robert C, Pennesi Mark E

机构信息

Casey Eye Institute, Oregon Health & Science University, Portland, OR, USA.

出版信息

Am J Ophthalmol Case Rep. 2020 Nov 17;21:100996. doi: 10.1016/j.ajoc.2020.100996. eCollection 2021 Mar.

Abstract

PURPOSE

To report the case of a ten-year old girl with torpedo maculopathy with a complete vitelliform lesion and describe associated optical coherence tomography (OCT), OCT angiography (OCTA), multifocal electroretinogram (ERG) and adaptive optics ophthalmoscopy (AOO) imaging of the lesion.

OBSERVATIONS

An asymptomatic ten-year old girl with visual acuity of 20/15 OU was referred for evaluation of possible Best's disease of her left eye. The unilaterality, location, and shape of the lesion was consistent with torpedo maculopathy. OCT and autofluorescence (AF) revealed that the entire lesion was composed of subretinal hyperreflective material that was hyperautofluorescent, consistent with vitelliform material. Within the boundary of the lesion, OCTA showed reduced choriocapillaris density while adjacent to the lesion, the choriocapillaris density was slightly increased. Microperimetry demonstrated normal sensitivity in both eyes, electrooculograms (EOG) were normal and multifocal ERG showed symmetrical mildly supernormal amplitudes. Additionally, AOO demonstrated that nasal to the lesion there were clusters of hyper-reflective areas, and immediately adjacent to the lesion cones were poorly resolved. However, there was a return to more normal photoreceptor architecture outside of the lesion.

CONCLUSIONS AND IMPORTANCE

Torpedo maculopathy lesions typically present with outer retinal attenuation and retinal pigmented epithelium (RPE) atrophy. Vitelliform material was recently observed for the first time in association with Torpedo maculopathy in a case report that described small vitelliform material at the periphery of the lesion. We report the second case of torpedo maculopathy associated with a vitelliform lesion and the first description of a torpedo lesion composed fully of presumed vitelliform material. We also describe findings of OCTA, multifocal ERG and AOO imaging in torpedo maculopathy with vitelliform lesion.

摘要

目的

报告一例患有伴有完整卵黄样病变的鱼雷样黄斑病变的10岁女孩病例,并描述该病变相关的光学相干断层扫描(OCT)、OCT血管造影(OCTA)、多焦视网膜电图(ERG)和自适应光学检眼镜(AOO)成像情况。

观察结果

一名无症状的10岁女孩,双眼视力为20/15,因左眼可能患有Best病而前来评估。病变的单侧性、位置和形状与鱼雷样黄斑病变相符。OCT和自发荧光(AF)显示整个病变由视网膜下高反射物质组成,该物质自发荧光增强,与卵黄样物质一致。在病变边界内,OCTA显示脉络膜毛细血管密度降低,而在病变相邻区域,脉络膜毛细血管密度略有增加。微视野检查显示双眼敏感度正常,眼电图(EOG)正常,多焦ERG显示对称的轻度超正常振幅。此外,AOO显示在病变鼻侧有高反射区域簇,紧邻病变处的视锥细胞分辨不清。然而,在病变外视网膜感光器结构恢复到更正常的状态。

结论与意义

鱼雷样黄斑病变通常表现为外层视网膜变薄和视网膜色素上皮(RPE)萎缩。在一篇描述病变周边小卵黄样物质的病例报告中,最近首次观察到卵黄样物质与鱼雷样黄斑病变相关。我们报告了第二例与卵黄样病变相关的鱼雷样黄斑病变病例,以及首次对完全由推测的卵黄样物质组成的鱼雷样病变的描述。我们还描述了伴有卵黄样病变的鱼雷样黄斑病变的OCTA、多焦ERG和AOO成像结果。

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