• 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

Spontaneous Resolution of Drug-Resistant Epilepsy in Patients with Sturge-Weber Syndrome.

作者信息

Alawadhi Abdulla, Poulin Chantal

机构信息

Department of Pediatrics, Neurology and Neurosurgery, McGill University, Montreal, Canada.

Dubai Medical College, Dubai, United Arab Emirates.

出版信息

Child Neurol Open. 2022 Oct 11;9:2329048X221129678. doi: 10.1177/2329048X221129678. eCollection 2022 Jan-Dec.

DOI:10.1177/2329048X221129678
PMID:36249668
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9554120/
Abstract

Sturge-Weber syndrome (SWS) is often associated with drug resistant epilepsy. The literature is unclear as to how often these patients can be weaned off of antiepileptic drugs (AEDs) to become seizure-free. We describe two patients with SWS. After initial treatment with various AEDs, breakthrough seizures still occurred. However, after periods with no seizure activity, they were weaned off of their medications. They have been off for 4 and 3 years and seizure-free for 13 and 12 years, respectively. No surgical procedure was necessary. We hypothesize that spontaneous involution or pathological disconnection of the vascular malformations might underly the patients' recovery. The initial aggressive therapy, close follow-up, choice of AEDs, or natural evolution of the disease may have played a role in their recovery. Therefore, in patients with SWS and lesional structural epilepsy, medication freedom is possible and invasive management options including surgery should be discussed carefully.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a343/9554120/c2b3cbb6b5e2/10.1177_2329048X221129678-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a343/9554120/977530642682/10.1177_2329048X221129678-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a343/9554120/c2b3cbb6b5e2/10.1177_2329048X221129678-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a343/9554120/977530642682/10.1177_2329048X221129678-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a343/9554120/c2b3cbb6b5e2/10.1177_2329048X221129678-fig2.jpg

相似文献

1
Spontaneous Resolution of Drug-Resistant Epilepsy in Patients with Sturge-Weber Syndrome.
Child Neurol Open. 2022 Oct 11;9:2329048X221129678. doi: 10.1177/2329048X221129678. eCollection 2022 Jan-Dec.
2
Sturge-Weber syndrome: an update on the relevant issues for neurosurgeons.斯特奇-韦伯综合征:神经外科医生相关问题的最新进展
Childs Nerv Syst. 2020 Oct;36(10):2553-2570. doi: 10.1007/s00381-020-04695-3. Epub 2020 Jun 21.
3
Proper Therapy Selection Improves Epilepsy Outcomes in Patients With Multilobar Sturge-Weber Syndrome.恰当的治疗选择可改善多脑叶脑颜面血管瘤病患者的癫痫结局。
Pediatr Neurol. 2023 Jun;143:6-12. doi: 10.1016/j.pediatrneurol.2023.02.011. Epub 2023 Feb 24.
4
Extent of Leptomeningeal Capillary Malformation is Associated With Severity of Epilepsy in Sturge-Weber Syndrome.软脑膜毛细血管畸形的范围与脑面血管瘤病癫痫严重程度相关。
Pediatr Neurol. 2021 Apr;117:64-71. doi: 10.1016/j.pediatrneurol.2020.12.012. Epub 2020 Dec 31.
5
Analysis of Sturge-Weber syndrome: A retrospective study of multiple associated variables.斯特奇-韦伯综合征分析:对多个相关变量的回顾性研究。
Neurologia. 2017 Jul-Aug;32(6):363-370. doi: 10.1016/j.nrl.2015.12.012. Epub 2016 Mar 8.
6
Focal lesionectomy as surgical treatment of epilepsy in patients with Sturge-Weber syndrome: a case-based systematic review and meta-analysis.Sturge-Weber 综合征患者癫痫灶切除术的手术治疗:基于病例的系统评价和荟萃分析。
Neurosurg Focus. 2022 May;52(5):E4. doi: 10.3171/2022.2.FOCUS21788.
7
Posterior quadrant disconnection surgery for Sturge-Weber syndrome.后部象限离断术治疗脑面血管瘤病。
Epilepsia. 2014 May;55(5):683-689. doi: 10.1111/epi.12547. Epub 2014 Feb 22.
8
Sturge-Weber syndrome.斯特奇-韦伯综合征
Childs Nerv Syst. 2006 Aug;22(8):909-21. doi: 10.1007/s00381-006-0143-2. Epub 2006 Jul 6.
9
Sirolimus as a Potential Treatment for Sturge-Weber Syndrome.西罗莫司治疗斯特奇-韦伯综合征的潜力。
J Craniofac Surg. 2021;32(1):257-260. doi: 10.1097/SCS.0000000000007034.
10
Sturge-Weber syndrome: clinical and radiological correlates in 86 patients.斯特奇-韦伯综合征:86例患者的临床与影像学关联
Ideggyogy Sz. 2013 Jan 30;66(1-2):53-7.

引用本文的文献

1
Sturge-Weber syndrome: updates in translational neurology.斯特奇-韦伯综合征:转化神经学的进展
Front Neurol. 2024 Dec 2;15:1493873. doi: 10.3389/fneur.2024.1493873. eCollection 2024.

本文引用的文献

1
ILAE official report: a practical clinical definition of epilepsy.ILAE 官方报告:癫痫的实用临床定义。
Epilepsia. 2014 Apr;55(4):475-82. doi: 10.1111/epi.12550. Epub 2014 Apr 14.
2
Sturge-Weber syndrome: from the past to the present.斯特奇-韦伯综合征:从过去到现在
Eur J Paediatr Neurol. 2014 May;18(3):257-66. doi: 10.1016/j.ejpn.2013.10.003. Epub 2013 Nov 7.
3
A perfusion-metabolic mismatch in Sturge-Weber syndrome: a multimodality imaging study.斯特奇-韦伯综合征中的灌注-代谢不匹配:一项多模态影像学研究。
Brain Dev. 2012 Aug;34(7):553-62. doi: 10.1016/j.braindev.2011.10.004. Epub 2011 Nov 8.
4
An infantile-onset, severe, yet sporadic seizure pattern is common in Sturge-Weber syndrome.婴儿期起病、严重但呈散发性的癫痫发作模式在斯-韦综合征中很常见。
Epilepsia. 2009 Sep;50(9):2154-7. doi: 10.1111/j.1528-1167.2009.02072.x. Epub 2009 Apr 6.
5
Sturge-Weber syndrome: age of onset of seizures and glaucoma and the prognosis for affected children.斯特奇-韦伯综合征:癫痫发作和青光眼的发病年龄以及患病儿童的预后
J Child Neurol. 1995 Jan;10(1):49-58. doi: 10.1177/088307389501000113.
6
Sturge-Weber syndrome: a study of cerebral glucose utilization with positron emission tomography.斯特奇-韦伯综合征:正电子发射断层扫描对脑葡萄糖利用的研究
J Pediatr. 1989 Feb;114(2):244-53. doi: 10.1016/s0022-3476(89)80790-5.
7
Neuroradiological findings in Sturge-Weber syndrome (SWS) and isolated pial angiomatosis.结节性硬化症(SWS)和孤立性软脑膜血管瘤病的神经放射学表现。
Neuropediatrics. 1991 Aug;22(3):115-20. doi: 10.1055/s-2008-1071429.
8
The epilepsy of Sturge-Weber syndrome: clinical features and treatment in 23 patients.
Acta Neurol Scand Suppl. 1992;140:18-22. doi: 10.1111/j.1600-0404.1992.tb04465.x.