Therapeutic Challenge in a Case of Recent Onset Refractory Cluster Seizures.

Journal of epilepsy research Pub Date : 2021-12-31 eCollection Date: 2021-12-01 DOI:10.14581/jer.21022
Sachin Sureshbabu, Muralikrishnan Veleri Padmanabhan, Jacob Alappat, Smilu Mohanlal, Sujith Janardhanan, Sellam Karunanidhi, Lakshminarayan Kannan, Dinesh Nayak, Biju Shekhar
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Abstract

A dilemma exists in context to the timing of surgery in a case presenting with explosive onset seizures secondary to a focal cortical dysplasia (FCD). This case report highlights the challenges faced in the management of a 4-year-old child with recent onset cluster seizures refractory to anti-epileptic drugs. A 4-year-old girl presented with an acute onset of cluster seizures (up to 32 in a day), semiologically characterized by tonic upper limb extension and laughter lasting for few seconds with no response to multiple anti-epileptic drugs. The clinical, electrographic, neuroimaging and interictal positron emission tomography data were concordant and consistent with a left middle frontal gyrus dysplasia which was successfully resected under electrocorticographic guidance. Patient is seizure free at 2 months of follow up. (Engel Class 1). Surgical resection is feasible and potentially more effective in the early phase of clinical presentation of FCD.

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一例新近发作的难治性丛集性癫痫的治疗挑战。
一个进退两难的情况下,手术的时机存在的情况下,表现为继发于局灶性皮质发育不良(FCD)的爆炸性发作癫痫发作。本病例报告强调了在管理一名4岁儿童与最近发作的丛集性癫痫难抗抗癫痫药物所面临的挑战。1例4岁女孩急性发作集束性癫痫发作(一天多达32次),符号学特征为强直性上肢伸展和持续数秒的笑声,对多种抗癫痫药物无反应。临床,电图,神经影像学和间期正电子发射断层扫描数据与左额叶中回发育不良一致,并在皮质电图引导下成功切除。随访2个月,患者无癫痫发作。手术切除在FCD临床表现的早期阶段是可行的,并且可能更有效。
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