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表现为持续性部分性癫痫的脑沟底部局灶性皮质发育不良的多模态特征,包括7T磁共振成像

Bottom-of-sulcus focal cortical dysplasia presenting as epilepsia partialis continua multimodality characterization including 7T MRI.

作者信息

Kelley Sarah A, Robinson Shenandoah, Crone Nathan E, Soares Bruno P

机构信息

Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

出版信息

Childs Nerv Syst. 2018 Jun;34(6):1267-1269. doi: 10.1007/s00381-018-3749-2. Epub 2018 Feb 14.

Abstract

INTRODUCTION

Bottom-of-sulcus focal cortical dysplasias are an under recognized, surgically treatable cause of focal epilepsy. Resection can dramatically reduce the seizure burden for children with refractory epilepsy, or eliminate seizures altogether.

MATERIAL AND METHODS

We report the case and present the results of multimodality evaluation of a 15-year-old young man who presented with long-standing partial epilepsy affecting his right leg, which over the years became refractory to therapy.

RESULTS

High-resolution 3T MRI images acquired as a dedicated epilepsyprotocol were initially interpreted as unremarkable. On further review by an experienced specialist aware of clinical and electroencephalographic findings, a subtle focal cortical dysplasia was identified at the bottom of a sulcus near the medial aspect of the left precentral gyrus. After confirmation of the extent of the lesion with PET and ultra-high field 7T MRI, the patient underwent cortical mapping and focal resection and remains free of seizures.

COCLUSIONS

This case emphasizes the need for a multidisciplinary approach to the evaluation of refractory focal epilepsy in children and highlights the potential role of ultra-high field 7T MRI in identifying the often subtle causative anatomic abnormalities.

摘要

引言

脑沟底部局灶性皮质发育不良是一种未被充分认识但可通过手术治疗的局灶性癫痫病因。手术切除可显著减轻难治性癫痫患儿的发作负担,或完全消除癫痫发作。

材料与方法

我们报告了一名15岁男性患者的病例,并展示了其多模态评估结果。该患者患有长期影响其右腿的部分性癫痫,多年来对治疗产生了耐药性。

结果

作为专门的癫痫检查方案所获取的高分辨率3T磁共振成像(MRI)图像最初被解读为无异常。一位熟悉临床和脑电图检查结果的经验丰富的专家进一步复查后,在左侧中央前回内侧附近脑沟底部发现了一个细微的局灶性皮质发育不良。通过正电子发射断层扫描(PET)和超高场7T MRI确认病变范围后,患者接受了皮质图谱绘制和局灶性切除手术,术后未再发作。

结论

该病例强调了对儿童难治性局灶性癫痫进行多学科评估的必要性,并突出了超高场7T MRI在识别通常较为细微的致病解剖异常方面的潜在作用。

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