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A hypermotor seizure with a focal orbital frontal lesion originating in the insula: a case report.

机译:运动异常性癫痫发作伴发局灶性眶额叶病变起源于孤立岛:一例病例报告。

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摘要

We present herein the case of a patient with a focal orbital frontal lesion on magnetic resonance imaging (MRI), but an insular onset of seizures. A 15-year-old boy suffered from hypermotor seizures for 9 years. In his seizures, he initially had a sensation that sounds were distant, and then his consciousness became impaired. After a short period of tonic activity, violent activities occurred, such as kicking or gripping some objects and shaking. MRI showed a focal cortical abnormality in the right orbital frontal lobe. [(18)F]FDG-PET revealed diffuse hypometabolism in the right frontal lobe, especially in the same site as the cortical lesion on MRI. The seizure onset zone was localized in the right anterior insula by intracranial recording. A resection of the right anterior insula and a partial disconnection of the frontal lobe were performed, rendering the patient seizure-free.
机译:我们在这里介绍的是在磁共振成像(MRI)上有局灶性眼眶额叶病变但出现癫痫发作的患者。一个15岁的男孩患有运动亢进症9年。癫痫发作时,他最初感觉到声音很远,然后意识丧失。短暂的进补活动后,发生了剧烈的活动,例如踢或抓住某些物体并摇动。 MRI显示右侧眶额叶有局灶性皮质异常。 [(18)F] FDG-PET显示右额叶弥漫性低代谢,尤其是与MRI上的皮层病变相同的部位。通过颅内记录,癫痫发作区位于右前岛。切除右前岛绝缘和额叶部分断开,使患者无癫痫发作。

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