Epilepsy surgery in Sturge-Weber syndrome with unilateral or bilateral asymmetric brain involvement: Boston Children's Hospital experience.

IF 6.6 1区 医学 Q1 CLINICAL NEUROLOGY
Epilepsia Pub Date : 2025-03-24 DOI:10.1111/epi.18387
Michelle Y Chiu, Isabelle Iannotti, Matheus D Soldatelli, Mustafa Sahin, Katrina Boyer, Morgan E Ryan, Bo Zhang, Masanori Takeoka, Joseph R Madsen, Scellig Stone, Sanjay Prabhu, Anna L Pinto
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Abstract

Objective: Sturge-Weber syndrome (SWS) is a neurocutaneous disorder caused by a somatic mosaic mutation in the GNAQ gene. Epilepsy is seen in 75%-80% of children with SWS, and they are at high risk of early onset seizures, status epilepticus, and drug-resistant epilepsy. Epilepsy surgery is an effective treatment, but timing and candidacy for epilepsy surgery remain controversial in this patient population. We examined the indications, trends, and outcomes of surgically treated patients with SWS at a large-volume tertiary pediatric hospital over >2 decades.

Methods: This retrospective cohort study includes all patients who have a clinical diagnosis of SWS, underwent epilepsy surgery, and were followed by a neurologist at Boston Children's Hospital with clinic visit(s) between January 2000 and April 2022. Chart review and descriptive statistics were performed, and epilepsy characteristics and magnetic resonance imaging findings of the surgical cohort were compared with a nonsurgical SWS cohort.

Results: Seventeen patients met the inclusion criteria, 12 with unilateral brain involvement (six right hemispheric) and five with bilateral asymmetric involvement. The average age at seizure onset was 7 months, and average age at first surgery was 29 months. Indication for epilepsy surgery was medically refractory epilepsy in all patients. Eleven hemispherectomies (seven anatomical, four functional) and six motor-sparing focal resections/disconnections were performed. After an average follow-up time of 7 years, Engel class I or II seizure outcome was achieved in 15 patients, including all five with bilateral asymmetric involvement. Five patients have discontinued antiseizure medications.

Significance: Outcomes after epilepsy surgery in children with SWS are robust and durable, with a low rate of complications. Both functional hemispherectomy and focal resections are effective in carefully selected patients, and patients with bilateral asymmetric involvement may have favorable outcomes.

伴有单侧或双侧脑不对称受损伤的斯特奇-韦伯综合征的癫痫手术:波士顿儿童医院的经验
目的:斯特奇-韦伯综合征(SWS)是一种由GNAQ基因体细胞镶嵌突变引起的神经皮肤疾病。75%-80%的SWS患儿有癫痫,他们有发生早发性癫痫、癫痫持续状态和耐药癫痫的高风险。癫痫手术是一种有效的治疗方法,但癫痫手术的时机和候选性在这一患者群体中仍存在争议。我们研究了20多年来一家大型三级儿科医院手术治疗的SWS患者的适应症、趋势和结果。方法:这项回顾性队列研究包括所有临床诊断为SWS、接受癫痫手术的患者,并在2000年1月至2022年4月期间由波士顿儿童医院的一名神经科医生随访。进行图表回顾和描述性统计,并将手术队列与非手术SWS队列的癫痫特征和磁共振成像结果进行比较。结果:17例患者符合纳入标准,其中12例为单侧脑受累(6例为右半脑),5例为双侧不对称受累。癫痫发作的平均年龄为7个月,首次手术的平均年龄为29个月。所有患者的手术指征均为医学难治性癫痫。11个半球切除术(7个解剖,4个功能)和6个保留运动的局部切除/断开。平均随访7年后,15例患者达到Engel I级或II级癫痫发作结局,包括所有5例双侧不对称受累患者。5名患者停用了抗癫痫药物。意义:SWS患儿癫痫手术后的预后稳健且持久,并发症发生率低。功能半球切除术和局灶性切除术对精心挑选的患者都是有效的,双侧不对称受累的患者可能有良好的结果。
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来源期刊
Epilepsia
Epilepsia 医学-临床神经学
CiteScore
10.90
自引率
10.70%
发文量
319
审稿时长
2-4 weeks
期刊介绍: Epilepsia is the leading, authoritative source for innovative clinical and basic science research for all aspects of epilepsy and seizures. In addition, Epilepsia publishes critical reviews, opinion pieces, and guidelines that foster understanding and aim to improve the diagnosis and treatment of people with seizures and epilepsy.
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