• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

福斯特·肯尼迪综合征:一种非典型表现。

Foster Kennedy Syndrome: An Atypical Presentation.

作者信息

Parafita-Fernández Alberto, Sampil Marta, Cores Carlos, Cores Francisco Javier, Viso Eloy

机构信息

*MD †MD, PhD Ophthalmology Department, Complejo Hospitalario de Pontevedra, Pontevedra, Spain (AP-F, MS, FJC, EV); and School of Medicine, University of Santiago de Compostela, Spain (CC).

出版信息

Optom Vis Sci. 2015 Dec;92(12):e425-30. doi: 10.1097/OPX.0000000000000731.

DOI:10.1097/OPX.0000000000000731
PMID:26540474
Abstract

PURPOSE

To describe an unusual presentation of Foster Kennedy syndrome (FKS; unilateral optic nerve atrophy with optic nerve edema in the other eye) with optic nerve atrophy and retinal vein occlusion. It is an example of how common clinical features can hide a rare condition or presentation of a disease. Foster Kennedy syndrome is uncommon. Therefore, a space-occupying lesion should be suspected when there is optic atrophy associated with acute pathology of the other eye.

CASE REPORT

A 56-year-old man presented with hemiretinal retinal vein occlusion in his right eye. He had previous optic nerve atrophy in his left eye attributed to nonarteritic anterior ischemic optic neuropathy. He lacked cardiovascular or prothrombotic risk factors. Consideration was given whether the presence of contralateral optic atrophy was associated with the retinal vein occlusion. A computed tomographic scan revealed a suprasellar mass. The tumor was excised and identified as meningioma.

CONCLUSIONS

Although typical FKS would present with optic nerve atrophy and contralateral optic nerve edema secondary to an intracranial mass, in this case, edema was replaced by a hemiretinal vein occlusion. In optic atrophy that does not show characteristic visual field alterations, typical symptoms, or the classic evolution of a given disease, diagnostic imaging may reveal the etiology. As FKS is uncommon, when there is optic atrophy associated with acute pathology of the other eye, a space-occupying lesion should be suspected.

摘要

目的

描述福斯特·肯尼迪综合征(FKS;一侧视神经萎缩伴对侧视神经水肿)合并视神经萎缩和视网膜静脉阻塞的一种不寻常表现。这是一个常见临床特征如何掩盖罕见疾病或疾病表现的例子。福斯特·肯尼迪综合征并不常见。因此,当存在与另一只眼的急性病变相关的视神经萎缩时,应怀疑有占位性病变。

病例报告

一名56岁男性,右眼出现半侧视网膜静脉阻塞。他左眼先前存在视神经萎缩,归因于非动脉性前部缺血性视神经病变。他没有心血管或血栓形成前危险因素。考虑对侧视神经萎缩的存在是否与视网膜静脉阻塞有关。计算机断层扫描显示鞍上有一肿块。肿瘤被切除,病理诊断为脑膜瘤。

结论

虽然典型的FKS表现为继发于颅内肿块的视神经萎缩和对侧视神经水肿,但在本病例中,水肿被半侧视网膜静脉阻塞所取代。在未表现出特征性视野改变、典型症状或特定疾病经典演变过程的视神经萎缩中,诊断性影像学检查可能揭示病因。由于FKS不常见,当存在与另一只眼的急性病变相关的视神经萎缩时,应怀疑有占位性病变。

相似文献

1
Foster Kennedy Syndrome: An Atypical Presentation.福斯特·肯尼迪综合征:一种非典型表现。
Optom Vis Sci. 2015 Dec;92(12):e425-30. doi: 10.1097/OPX.0000000000000731.
2
Foster Kennedy syndrome and optociliary shunt vessels in a patient with an olfactory groove meningioma.一名患有嗅沟脑膜瘤的患者出现福斯特·肯尼迪综合征及视网膜睫状分流血管。
Ophthalmologica. 1991;202(3):125-31. doi: 10.1159/000310188.
3
An unusual presentation of nonarteritic ischemic optic neuropathy with subretinal fluid treated with intravitreal bevacizumab.玻璃体腔内注射贝伐单抗治疗伴有视网膜下液的非动脉炎性缺血性视神经病变的罕见表现
Indian J Ophthalmol. 2016 Jan;64(1):87-8. doi: 10.4103/0301-4738.178143.
4
Combined treatment with intravitreal bevacizumab and laser photocoagulation for exudative maculopathy in facioscapulohumeral muscular dystrophy.玻璃体内注射贝伐单抗联合激光光凝治疗面肩肱型肌营养不良症的渗出性黄斑病变。
Ophthalmic Genet. 2017 Sep-Oct;38(5):490-493. doi: 10.1080/13816810.2017.1279183. Epub 2017 Jan 25.
5
Foster Kennedy syndrome and an optociliary vein in a patient with a falx meningioma.一名患有镰旁脑膜瘤的患者出现福斯特·肯尼迪综合征及眼睫状静脉。
J Clin Neuroophthalmol. 1984 Jun;4(2):97-101.
6
Central retinal vein occlusion in an otherwise healthy child treated successfully with a single injection of bevacizumab.一名原本健康的儿童发生视网膜中央静脉阻塞,经单次注射贝伐单抗成功治愈。
J AAPOS. 2015 Oct;19(5):473-4. doi: 10.1016/j.jaapos.2015.04.012.
7
Subthreshold grid laser versus intravitreal bevacizumab as second-line therapy for macular edema in branch retinal vein occlusion recurring after conventional grid laser treatment.阈下格栅样激光与玻璃体内注射贝伐单抗作为传统格栅样激光治疗后复发的视网膜分支静脉阻塞性黄斑水肿的二线治疗方法比较
Graefes Arch Clin Exp Ophthalmol. 2015 Oct;253(10):1647-51. doi: 10.1007/s00417-014-2845-6. Epub 2014 Nov 11.
8
Combined intravitreal bevacizumab and grid laser photocoagulation for macular edema secondary to branch retinal vein occlusion.玻璃体内注射贝伐单抗联合格栅样激光光凝治疗视网膜分支静脉阻塞继发黄斑水肿
Eur J Ophthalmol. 2012 Jul-Aug;22(4):607-14. doi: 10.5301/ejo.5000085.
9
Prospective study of intravitreal triamcinolone acetonide versus bevacizumab for macular edema secondary to central retinal vein occlusion.前瞻性研究曲安奈德与贝伐单抗治疗视网膜中央静脉阻塞继发黄斑水肿。
Retina. 2011 May;31(5):838-45. doi: 10.1097/IAE.0b013e3181f4420d.
10
Comparative study of combined bevacizumab/targeted photocoagulation vs bevacizumab alone for macular oedema in ischaemic branch retinal vein occlusions.贝伐单抗联合靶向光凝与单纯贝伐单抗治疗缺血性视网膜分支静脉阻塞所致黄斑水肿的对比研究
Acta Ophthalmol. 2016 May;94(3):e225-30. doi: 10.1111/aos.12721. Epub 2015 May 19.