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与卡斯特曼病相关的视神经病变

Optic neuropathy associated with Castleman disease.

作者信息

Kim Ungsoo, Hwang Jeong-Min

机构信息

Department of Ophthalmology, Kim's Eye Hospital, Konyang University College of Medicine, Seoul, Korea.

出版信息

Korean J Ophthalmol. 2010 Aug;24(4):256-9. doi: 10.3341/kjo.2010.24.4.256. Epub 2010 Aug 3.

Abstract

A 44-year-old woman with Castleman disease presented with acute visual loss in the left eye. A full ophthalmologic examination and imaging were performed. Visual acuity was 20/20 in the right eye and 20/100 in the left eye. Total dyschromatopsia, a relative afferent pupillary defect, and a cecocentral scotoma were observed in the left eye. Mild disc edema, without leaking during fluorescein angiography, was also observed. Magnetic resonance imaging revealed a small cystic epidermoid-like lesion in the right prepontine and suprasellar cistern. Her visual acuity did not improve and deteriorated to 20/200 in the left eye at 22 months after the initial visual loss. Optic neuropathy may rarely be associated with Castleman disease and suggests a poor prognosis.

摘要

一名患有Castleman病的44岁女性出现左眼急性视力丧失。进行了全面的眼科检查和影像学检查。右眼视力为20/20,左眼视力为20/100。左眼观察到全色盲、相对性传入瞳孔障碍和中心暗点。还观察到轻度视盘水肿,在荧光素血管造影期间无渗漏。磁共振成像显示右侧脑桥前和鞍上池有一个小的囊性表皮样病变。在最初视力丧失22个月后,她的视力没有改善,左眼视力恶化为20/200。视神经病变很少与Castleman病相关,提示预后不良。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b62/2916111/d3310451bd35/kjo-24-256-g001.jpg

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