A Case Report of Sturge-Weber Syndrome With Gelastic SeizuresWang, Fei MMed*; Gui, Songbai MD†Neurosurgery Quarterly: May 2015 - Volume 25 - Issue 2 - p 197–199 doi: 10.1097/WNQ.0000000000000023 Case Report Abstract Author InformationAuthors Article MetricsMetrics 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. *Beijing Neurosurgical Institute †The Neurosurgical Department of Beijing Tiantan Hospital, Capital Medical University, Beijing, China The authors declare no conflict of interest. Reprints: Songbai Gui, MD, The Neurosurgical Department of Beijing Tiantan Hospital, Capital Medical University, 100050 Beijing, China (e-mail: email@example.com). Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved.