斯特奇-韦伯综合征患者耐药癫痫的自发消退。

Child neurology open Pub Date : 2022-10-11 eCollection Date: 2022-01-01 DOI:10.1177/2329048X221129678
Abdulla Alawadhi, Chantal Poulin
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引用次数: 1

摘要

斯特奇-韦伯综合征(SWS)常与耐药癫痫相关。文献尚不清楚这些患者多久可以停止使用抗癫痫药物(aed)以避免癫痫发作。病例描述:我们描述了两例SWS患者。在最初使用各种抗癫痫药治疗后,仍然发生突破性癫痫发作。然而,在一段时间没有癫痫发作活动后,他们就停止了药物治疗。他们已经分别休息了4年和3年,13年和12年没有癫痫发作。无需外科手术。结论:我们推测血管畸形的自然复发或病理性断裂可能是患者康复的基础。最初的积极治疗、密切随访、选择aed或疾病的自然演变可能对他们的康复起了作用。因此,对于SWS和病变结构性癫痫患者,自由用药是可能的,应仔细讨论包括手术在内的侵入性治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

Introduction: 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. Case Description: 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. Conclusion: 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.

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