Liu Qingzhu, Zhu Renqing, Wang Yao, Yu Hao, Liu Chang, Sun Yu, Wang Yi, Liu Xiaoyan, Wang Shuang, Ji Taoyun, Cai Lixin
Pediatric Epilepsy Center, Peking University First Hospital, Beijing, China.
National Children's Medical Center, Children's Hospital of Fudan University, Shanghai, China.
Epilepsia. 2025 Jul;66(7):2190-2197. doi: 10.1111/epi.18368. Epub 2025 Apr 16.
Peri-Rolandic epilepsy in pediatric patients presents unique surgical challenges due to the involvement of eloquent cortical regions, where resective surgery carries risks of permanent neurological deficits. This study investigates lesion distribution, surgical outcomes, and the relationship between lesion location and postoperative motor function in children undergoing surgery for drug-resistant epilepsy in the peri-Rolandic area.
This retrospective study included 152 pediatric patients who underwent craniotomy for peri-Rolandic epilepsy between September 2014 and January 2023. Patients met the criteria of drug-resistant epilepsy, peri-Rolandic surgical resection, and a minimum follow-up of 6 months. Preoperative evaluations included video electroencephalography (VEEG), magnetic resonance imaging, and positron emission tomography, with invasive monitoring in select cases. Motor function and seizure outcomes were assessed using Engel classification and multivariate logistic regression to examine correlations between lesion location, motor deficits, and seizure prognosis.
Lesions were most commonly found in the central operculum, affecting 66% of patients. Postoperative seizure freedom (Engel class I) was achieved in 80% of cases. Among patients with preoperative motor deficits (28%), 39.5% fully recovered after surgery, whereas 27.9% experienced permanent severe impairments. Resecting lesions in the precentral gyrus, paracentral lobule, and premotor cortex was significantly associated with long-term motor dysfunction. There was no significant association between the location of the lesion and postoperative seizure control.
Surgery for peri-Rolandic epilepsy in children is effective in achieving seizure control, although it carries risks of motor dysfunction. Lesion location should be carefully considered to optimize surgical outcomes, balancing seizure control with the preservation of motor function.
小儿罗兰多区周围癫痫因涉及明确的皮质区域而带来独特的手术挑战,在这些区域进行切除性手术存在永久性神经功能缺损的风险。本研究调查了罗兰多区周围药物难治性癫痫患儿手术中的病灶分布、手术结果以及病灶位置与术后运动功能之间的关系。
这项回顾性研究纳入了2014年9月至2023年1月期间因罗兰多区周围癫痫接受开颅手术的152例儿科患者。患者符合药物难治性癫痫、罗兰多区周围手术切除以及至少随访6个月的标准。术前评估包括视频脑电图(VEEG)、磁共振成像和正电子发射断层扫描,部分病例进行了侵入性监测。使用恩格尔分类法评估运动功能和癫痫发作结果,并进行多因素逻辑回归分析,以检查病灶位置、运动功能缺损与癫痫发作预后之间的相关性。
病灶最常见于中央脑岛,66%的患者受影响。80%的病例术后实现了癫痫发作自由(恩格尔I级)。术前有运动功能缺损的患者(28%)中,39.5%术后完全恢复,而27.9%出现永久性严重损伤。切除中央前回、中央旁小叶和运动前区的病灶与长期运动功能障碍显著相关。病灶位置与术后癫痫控制之间无显著关联。
小儿罗兰多区周围癫痫手术在实现癫痫控制方面是有效的,尽管存在运动功能障碍的风险。应仔细考虑病灶位置以优化手术结果,在癫痫控制与运动功能保留之间取得平衡。