Service de Neurochirurgie, Hôpital Erasme, Université Libre de Bruxelles, Route de Lennik 808, B, 1070, Brussels, Belgium.
Department of Neurosurgery, Boston Children's Hospital, Harvard Medical School, 300 Longwood Avenue, Boston, MA, 02115, USA.
Childs Nerv Syst. 2022 Jul;38(7):1365-1370. doi: 10.1007/s00381-022-05532-5. Epub 2022 Apr 21.
Focal cortical dysplasia (FCD) is a common etiology of refractory epilepsy, particularly in children. Surgical management is potentially curative, but poses the challenge of distinguishing the border between ictogenic regions of dysplasia and functionally critical brain tissue. Bottom-of-a-sulcus dysplasia (BOSD) amplifies this challenge, due to difficulties in physiologic mapping of the deep tissue.
We report a one-stage resection of a dysplasia-associated seizure focus abutting and involving the hand and face primary motor cortex. In doing so, we describe our surgical planning integrating neuronavigated transcranial magnetic stimulation (nTMS) for functional motor mapping, combined with intraoperative ultrasonography, intracranial electroencephalography, and magnetic resonance imaging (MRI). A 5-year-old girl with intractable focal epilepsy was referred to our comprehensive epilepsy program. Despite attentive pharmacotherapy, she experienced status epilepticus and up to 70 seizures per day, accompanied by multiple side effects from her antiseizure medication. A right frontal BOSD in close proximity to the hand motor area of the precentral gyrus was identified on MRI. Postoperatively, she is seizure-free for over 1 year with no hand deficit.
Although technically complex, single-stage resection taking advantage of comprehensive surgical planning with optimized fusion of functional mapping and intraoperative modalities merits consideration given the invasiveness of a two-stage approach for limited added value. Integrated pre-surgical nTMS allowed for mapping of eloquent cortex without invasive electrocortical stimulation.
局灶性皮质发育不良(FCD)是难治性癫痫的常见病因,尤其是在儿童中。手术治疗具有潜在的治愈性,但存在区分发育不良致痫区和功能关键脑组织边界的挑战。底沟型发育不良(BOSD)增加了这一挑战,因为深部组织的生理映射存在困难。
我们报告了一例与手和面部初级运动皮层相邻并累及的发育相关性癫痫灶的一期切除术。在这样做的过程中,我们描述了我们的手术计划,包括经颅磁刺激(nTMS)进行功能运动映射,结合术中超声、颅内脑电图和磁共振成像(MRI)。一名 5 岁女孩因难治性局灶性癫痫被转诊至我们的综合癫痫项目。尽管进行了精心的药物治疗,她仍经历癫痫持续状态和每天多达 70 次发作,同时伴有抗癫痫药物的多种副作用。MRI 显示右侧额部 BOSD 紧邻中央前回的手部运动区。术后,她无癫痫发作已超过 1 年,且手部无缺陷。
尽管技术上复杂,但利用功能映射和术中模式的综合手术计划进行单阶段切除,考虑到两阶段方法的侵入性和有限的附加价值,值得考虑。术前整合 nTMS 允许在不进行侵入性皮质电刺激的情况下对功能区进行映射。