Zhang Hua, Yao Qinghe, Zhao Xin, Jin Xiaorong, Wang Chao, Guo Heng, You Yu, Wang Haiwei, Gao Guodong
Department of Neurosurgery, Tangdu Hospital, The Fourth Military Medical University, Shaanxi Province, China.
Epilepsy Res. 2008 Dec;82(2-3):211-4. doi: 10.1016/j.eplepsyres.2008.06.013. Epub 2008 Aug 30.
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.
我们在此呈现一例磁共振成像(MRI)显示眶额部有局灶性病变,但癫痫发作起始于脑岛的患者。一名15岁男孩患有运动增多性癫痫9年。在发作时,他最初感觉声音遥远,随后意识受损。经过短时间的强直活动后,会出现剧烈动作,如踢打或抓握物体并摇晃。MRI显示右侧眶额叶有局灶性皮质异常。[(18)F]FDG-PET显示右侧额叶弥漫性代谢减低,尤其是与MRI上皮质病变相同的部位。通过颅内记录将癫痫发作起始区定位于右侧前脑岛。对右侧前脑岛进行了切除,并对额叶进行了部分离断,患者术后无癫痫发作。