Koueik Joyce, Youn Youngwon, Rebsamen Susan, Wallace Adam N, Kney Adam, Knox Andrew T, Hsu David A, Ahmed Raheel
Department of Neurological Surgery, School of Medicine and Public Health, University of Wisconsin, 1675 Highland Ave, Madison, WI, 53792-3252, USA.
Department of Radiology, School of Medicine and Public Health, University of Wisconsin, Madison, WI, USA.
Childs Nerv Syst. 2025 Sep 11;41(1):275. doi: 10.1007/s00381-025-06925-y.
We present a case series of pediatric subjects with drug resistant epilepsy (DRE) that underwent surgical resection utilizing intraoperative MRI (IOMRI) to confirm resection of the hypothesized epileptogenic zone (EZ). Clinical, radiographic and seizure control outcome measures are presented to support the hypothesis that inclusion of IOMRI enables assessment and confirmation of total resection of the hypothesized EZ and eliminates the incidence of inadvertent incomplete resections.
We reviewed records for all pediatric patients (< 21 years) with DRE who underwent surgical resection between Dec 2017 and Aug 2023.
Thirty subjects with a mean follow-up duration of 4.2 ± 0.3 years (range: 1.6-7.3 years) were identified. The most prevalent pathological subtypes were focal cortical dysplasia (33%) followed by gliosis (30%). Phase II evaluation was undertaken in 24 subjects (80%). IOMRI revealed incomplete resection of the intended EZ in 73% (n = 22) of subjects, who then underwent additional resection. Two subjects underwent an incomplete resection due to functional constraints. Seizure improvement (Engel I + II) following surgery was observed in 90% of subjects with 80% (n = 24) subjects with Engel I outcome. An incomplete resection due to functional overlap or widespread network was associated with Engel III outcome in 3 subjects (10%).
Intraoperative imaging during surgical resection for DRE eliminates the incidence of inadvertent incomplete resections and reduces the risk of early seizure recurrence. Our results over an extended follow-up period, elucidate long-term epilepsy outcomes for DRE surgery with IOMRI assistance, that are associated with a low incidence of repeat resection due to epilepsy recurrence.
我们报告一组药物难治性癫痫(DRE)儿科患者病例系列,这些患者接受了手术切除,术中使用磁共振成像(IOMRI)以确认假定致痫区(EZ)的切除情况。展示临床、影像学和癫痫控制结果指标,以支持以下假设:使用IOMRI能够评估并确认假定EZ的完全切除,并消除无意的不完全切除的发生率。
我们回顾了2017年12月至2023年8月期间接受手术切除的所有DRE儿科患者(<21岁)的记录。
确定了30名患者,平均随访时间为4.2±0.3年(范围:1.6 - 7.3年)。最常见的病理亚型是局灶性皮质发育不良(33%),其次是胶质增生(30%)。24名患者(80%)进行了II期评估。IOMRI显示73%(n = 22)的患者预期EZ切除不完全,这些患者随后接受了额外切除。两名患者由于功能限制接受了不完全切除。90%的患者术后癫痫发作得到改善(Engel I + II),其中80%(n = 24)的患者达到Engel I结局。3名患者(10%)因功能重叠或广泛网络导致的不完全切除与Engel III结局相关。
DRE手术切除期间的术中成像消除了无意的不完全切除的发生率,并降低了早期癫痫复发的风险。我们在延长随访期内的结果阐明了在IOMRI辅助下DRE手术的长期癫痫结局,其与因癫痫复发导致的再次切除发生率低相关。