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特发性旁中心急性中黄斑病变的光学成像:一位中国年轻男性患者的病例报告及文献复习

The optical imaging of idiopathic paracentral acute middle maculopathy in a Chinese young man and review of the literature.

机构信息

Department of Geriatrics, The First Affiliated Hospital of China Medical University, No. 155 Nanjing Bei Street, Heping District, Shenyang City, Liaoning Province, 110001, PR China; The Key Laboratory of Endocrine Diseases in Liaoning Province, The First Hospital of China Medical University, No. 155 Nanjing Bei Street, Heping District, Shenyang City, Shenyang, 110001, PR China.

Department of Ophthalmology, the First Affiliated Hospital of China Medical University, No. 155 Nanjing Bei Street, Heping District, Shenyang City, Liaoning Province, 110001, PR China; Diabetic Eye Center of Liaoning Province, No. 155 Nanjing Bei Street, Heping District, Shenyang City, Liaoning Province, 110001, PR China.

出版信息

Photodiagnosis Photodyn Ther. 2017 Sep;19:383-387. doi: 10.1016/j.pdpdt.2017.07.004. Epub 2017 Jul 18.

Abstract

We report a case of idiopathic paracentral acute middle maculopathy with typical optical imaging and clinical features. A 26-year-old Chinese policeman presented with a 20-day history of paracentral scotoma in the left eye after early wake-up and long-time working in front of computer the day before. He experienced sudden-onset strong flash in his left eye. Paracentral scotoma appeared in his left eye after 6hours of rest. The general history was negative. His best corrected visual acuity was 20/20 OU. Anterior segment, dilated fundus examination, papillary evaluation and intraocular pressure were normal. Fuorescein angiography and blue light fundus autofluorescence showed no significant abnormality. In multicolor photography, the lesion was visible on the monochromic infrared/blue reflectance images and not clear in green reflectance. The 10 degree visual field examination revealed superior paracentral relative scotoma. Multifocal electroretinogram revealed reduced response in central area in the left eye. Spectral-domain optical coherence tomography showed that hyperreflective plaque was present at the IPL/INL/OPL level with hyperreflective point at the GCL. The plaque became thinner 3 months later and diminished 6 months later with obviously atrophied INL. In the 3 months follow-up, transverse scan revealed that there was a well-demarcated hypo-refractive lesion in IPL and hyper-refractive lesion in INL. OCTA revealed the deceased flow signal intensity of focal deep capillaries. En face OCT imaging of the left eye revealed a relative well-defined, hypo-refractive lesion and non-flow area localized at the level of the deep capillary plexus.

摘要

我们报告了一例特发性旁中心急性中黄斑病变的病例,其具有典型的光学成像和临床特征。一位 26 岁的中国警察因前一天早起后在电脑前长时间工作,左眼出现 20 天的旁中心暗点和 6 小时休息后出现左眼突发性强闪光而就诊。左眼出现旁中心暗点。他的最佳矫正视力为双眼 20/20。眼前节、散瞳眼底检查、视乳头评估和眼压均正常。荧光素血管造影和蓝光眼底自发荧光未见明显异常。多光谱摄影中,病变在单色红外/蓝光反射图像上可见,在绿光反射图像上不清楚。10 度视野检查显示上方旁中心相对暗点。多焦视网膜电图显示左眼中心区反应减弱。光谱域光学相干断层扫描显示 IPL/INL/OPL 水平存在高反射斑块,GCL 存在高反射点。3 个月后斑块变薄,6 个月后明显变薄,INL 明显萎缩。在 3 个月的随访中,横断扫描显示 IPL 存在界限清楚的低反射病变,INL 存在高反射病变。OCTA 显示局部深毛细血管的血流信号强度降低。左眼的面扫描 OCT 成像显示相对界限清楚的低反射病变和无血流区域定位于深毛细血管丛水平。

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