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使用术中超声和单深度电极记录对沟底发育异常进行术中定义——技术说明

Intraoperative definition of bottom-of-sulcus dysplasia using intraoperative ultrasound and single depth electrode recording - A technical note.

作者信息

Miller Dorothea, Carney Patrick, Archer John S, Fitt Gregory J, Jackson Graeme D, Bulluss Kristian J

机构信息

Department of Neurosurgery, Austin Health, Heidelberg, Victoria, Australia; Department of Neurosurgery, Essen University Hospital, Essen, Nordrhein-Westfalen, Germany.

Department of Neurology, Austin Health, Heidelberg, Victoria, Australia; Eastern Health Clinical School, Faculty of Medicine, Nursing and Health Sciences, Monash University, Box Hill, Victoria, Australia; The Florey Institute of Neuroscience and Mental Health, Melbourne Brain Centre, Heidelberg, Victoria, Australia.

出版信息

J Clin Neurosci. 2018 Feb;48:191-195. doi: 10.1016/j.jocn.2017.10.045. Epub 2017 Nov 11.

Abstract

Bottom of sulcus dysplasias (BOSDs) are localized focal cortical dysplasias (FCDs) centred on the bottom of a sulcus that can be highly epileptogenic, but difficult to delineate intraoperatively. We report on a patient with refractory epilepsy due to a BOSD, successfully resected with the aid of a multimodal surgical approach using neuronavigation based on MRI and PET, intraoperative ultrasound (iUS) and electrocorticography (ECoG) using depth electrodes. The lesion could be visualized on iUS showing an increase in echogenicity at the grey-white matter junction. IUS demonstrated the position of the depth electrode in relation to the lesion. Depth electrode recording showed almost continuous spiking. Thus, intraoperative imaging and electrophysiology helped confirm the exact location of the lesion. Post-resection ultrasound demonstrated the extent of the resection and depth electrode recording did not show any epileptiform activity. Thus, both techniques helped assess completeness of resection. The patient has been seizure free since surgery. Using a multimodal approach including iUS and ECoG is a helpful adjunct in surgery for BOSD and may improve seizure outcome.

摘要

脑沟底部发育异常(BOSDs)是一种局限性局灶性皮质发育异常(FCDs),以脑沟底部为中心,具有高度致痫性,但术中难以界定。我们报告了一名因BOSD导致难治性癫痫的患者,通过基于MRI和PET的神经导航、术中超声(iUS)以及使用深度电极的皮质脑电图(ECoG)等多模态手术方法成功切除病变。病变在iUS上可见,表现为灰白质交界处回声增强。iUS显示了深度电极相对于病变的位置。深度电极记录显示几乎持续的棘波发放。因此,术中成像和电生理有助于确认病变的确切位置。切除术后超声显示了切除范围,深度电极记录未显示任何癫痫样活动。因此,这两种技术都有助于评估切除的完整性。该患者术后无癫痫发作。采用包括iUS和ECoG在内的多模态方法对BOSD手术是一种有益的辅助手段,可能改善癫痫治疗效果。

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