• 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

多发性视网膜小动脉闭塞与原发性抗磷脂综合征和凝血因子V莱顿突变并存相关。

Multiple retinal arteriolar occlusions associated with coexisting primary antiphospholipid syndrome and factor V Leiden mutation.

作者信息

Dori D, Beiran I, Gelfand Y, Lanir N, Scharf J, Miller B, Brenner B

机构信息

Department of Ophthalmology, Rambam Medical Center, Haifa, Israel.

出版信息

Am J Ophthalmol. 2000 Jan;129(1):106-8. doi: 10.1016/s0002-9394(99)00278-0.

DOI:10.1016/s0002-9394(99)00278-0
PMID:10653428
Abstract

PURPOSE

To investigate a case of a young woman with both primary antiphospholipid syndrome and factor V Leiden mutation who developed multiple retinal arteriolar occlusions.

METHOD

Case report of a 25-year-old woman with history and laboratory tests confirming the diagnosis of both primary antiphospholipid syndrome and factor V Leiden mutation who presented with blurred vision in both eyes.

RESULTS

Multiple retinal arteriolar occlusions were observed in both of her eyes. The patient was treated first with heparin and then with warfarin.

CONCLUSIONS

Primary antiphospholipid syndrome and factor V Leiden mutation, as well as other forms of thrombophilia, should be considered in the differential diagnosis of unexplained retinal vascular occlusions. The coexistence of several thrombophilic disorders may carry a particularly high risk for thrombotic manifestations.

摘要

目的

调查一名患有原发性抗磷脂综合征和凝血因子V莱顿突变的年轻女性发生多发性视网膜小动脉阻塞的病例。

方法

对一名25岁女性的病例报告,其病史和实验室检查证实诊断为原发性抗磷脂综合征和凝血因子V莱顿突变,该患者双眼出现视力模糊。

结果

在她的双眼均观察到多发性视网膜小动脉阻塞。患者首先接受肝素治疗,然后接受华法林治疗。

结论

在不明原因的视网膜血管阻塞的鉴别诊断中,应考虑原发性抗磷脂综合征和凝血因子V莱顿突变以及其他形式的血栓形成倾向。几种血栓形成性疾病的共存可能会带来特别高的血栓形成表现风险。

相似文献

1
Multiple retinal arteriolar occlusions associated with coexisting primary antiphospholipid syndrome and factor V Leiden mutation.多发性视网膜小动脉闭塞与原发性抗磷脂综合征和凝血因子V莱顿突变并存相关。
Am J Ophthalmol. 2000 Jan;129(1):106-8. doi: 10.1016/s0002-9394(99)00278-0.
2
Reversal of nonarteritic anterior ischemic optic neuropathy associated with coexisting primary antiphospholipid syndrome and Factor V Leiden mutation.合并原发性抗磷脂综合征和凝血因子V莱顿突变的非动脉炎性前部缺血性视神经病变的逆转
Am J Ophthalmol. 2001 May;131(5):671-3. doi: 10.1016/s0002-9394(00)00873-4.
3
Consecutive central retinal artery and vein occlusions in primary antiphospholipid syndrome.原发性抗磷脂综合征中的连续性视网膜中央动脉和静脉阻塞
Retina. 2002 Dec;22(6):784-6. doi: 10.1097/00006982-200212000-00016.
4
[Myocardial infarction as an initial symptom of antiphospholipid syndrome, factor V Leiden mutation, and hyperhomocysteinemia].
Pol Arch Med Wewn. 2004 Jan;111(1):63-7.
5
[Retinal artery occlusion and anterior ischemic optic neuropathy associated with factor V Leiden mutation: A case report].[视网膜动脉阻塞及前部缺血性视神经病变与凝血因子V莱顿突变相关:一例报告]
J Fr Ophtalmol. 2020 Apr;43(4):294-297. doi: 10.1016/j.jfo.2019.08.020. Epub 2020 Feb 24.
6
Bilateral cilioretinal artery occlusion in antiphospholipid syndrome.抗磷脂综合征中的双侧睫状视网膜动脉阻塞
Retina. 2006 Jan;26(1):104-6. doi: 10.1097/00006982-200601000-00018.
7
Factor V Leiden mutation and antiphospholipid syndrome: risk factors for atherosclerotic and arterial thromboembolic disease.凝血因子V莱顿突变与抗磷脂综合征:动脉粥样硬化和动脉血栓栓塞性疾病的危险因素。
J Vasc Interv Radiol. 2009 Aug;20(8):1097-8. doi: 10.1016/j.jvir.2009.04.073. Epub 2009 Jul 2.
8
Anticoagulant therapy after retinal vein occlusion in patients with protein S deficiency (Protein S deficiency with homozygous factor V Leiden mutation in central retinal vein occlusion. Vol. 42[4]).蛋白 S 缺乏患者视网膜静脉阻塞后的抗凝治疗(中央视网膜静脉阻塞合并纯合子因子 V 莱顿突变的蛋白 S 缺乏症。第 42 卷[4])
Can J Ophthalmol. 2007 Dec;42(6):875; author reply 876. doi: 10.3129/i07-175.
9
Bilateral occlusive retinal vasculitis in a patient with primary antiphospholipid antibody syndrome.一名原发性抗磷脂抗体综合征患者的双侧闭塞性视网膜血管炎。
Can J Ophthalmol. 2012 Dec;47(6):e60-1. doi: 10.1016/j.jcjo.2012.07.010. Epub 2012 Sep 29.
10
Branch retinal arteriolar occlusion associated with familial factor V Leiden polymorphism and positive rheumatoid factor.视网膜分支小动脉阻塞与家族性凝血因子V莱顿多态性及类风湿因子阳性相关。
Arch Ophthalmol. 1999 Jul;117(7):971-3.

引用本文的文献

1
A 12-year nationwide cohort study on the association between central retinal artery occlusion and cancer.一项关于中央视网膜动脉阻塞与癌症之间关联的 12 年全国队列研究。
Graefes Arch Clin Exp Ophthalmol. 2023 Jul;261(7):1893-1900. doi: 10.1007/s00417-023-05984-8. Epub 2023 Feb 7.
2
Retinal artery and vein thrombotic occlusion during pregnancy: markers for familial thrombophilia and adverse pregnancy outcomes.妊娠期视网膜动静脉血栓形成性闭塞:家族性易栓症及不良妊娠结局的标志物
Clin Ophthalmol. 2016 May 23;10:935-8. doi: 10.2147/OPTH.S106164. eCollection 2016.
3
Hemi-central retinal artery occlusion in young adults.
中青年患者半侧中央视网膜动脉阻塞。
Indian J Ophthalmol. 2010 Sep-Oct;58(5):425-32. doi: 10.4103/0301-4738.67069.
4
What causes the antiphospholipid syndrome?抗磷脂综合征的病因是什么?
Curr Rheumatol Rep. 2001 Aug;3(4):293-300. doi: 10.1007/s11926-001-0033-2.
5
Thrombophilia: genetic polymorphisms and their association with retinal vascular occlusive disease.血栓形成倾向:基因多态性及其与视网膜血管阻塞性疾病的关联
Br J Ophthalmol. 2001 Jul;85(7):883-6. doi: 10.1136/bjo.85.7.883.