资源类型：
期刊
文章类型：
论著
机构：
[a]Beijing Neurosurgical Institute, Beijing Tiantan Hospital, Capital Medical University, Beijing, China
研究所
北京市神经外科研究所
首都医科大学附属天坛医院
[b]Neurosurgical Department, Beijing Tiantan Hospital, Capital Medical University, Beijing, 100050, China
重点科室
诊疗科室
神经外科
神经外科
首都医科大学附属天坛医院
ISSN：
1050-6438
关键词：
gelastic seizure
Sturge-Weber syndrome
摘要：
Sturge-Weber syndrome (SWS) is characterized by the association of a facial capillary malformation with a vascular malformation of the eye, and/or vascular malformation of the brain. We report a case of 7-year-old boy who presented with a deep purple nevus of 5×7 cm on left side of the face since birth and gelastic seizures. Clinically, gelastic episodes were diagnosed secondary to SWS that improved with aggressive seizure management and low-dose aspirin use. We have attempted to identify the pathophysiology of the rare episodes in SWS. The case report underlines that the epileptic phenomena of the SWS may manifest with gelastic seizures and need correct identification and appropriate response for optimal management by doctors. © 2013 Wolters Kluwer Health, Inc.
第一作者：
Wang, F
推荐引用方式(GB/T 7714)：
Wang F,Gui S.A case report of sturge-weber syndrome with gelastic seizures[J].2015,25(2):doi:10.1097/WNQ.0000000000000023.
APA：
Wang, F&Gui, S.(2015).A case report of sturge-weber syndrome with gelastic seizures.,25,(2)
MLA：
Wang, F,et al."A case report of sturge-weber syndrome with gelastic seizures". 25..2(2015)
