Avila J O, Radvany J, Huck F R, Pires de Camargo C H, Marino R, Ragazzo P C, Riva D
Acta Neurochir Suppl (Wien). 1980;30:137-43. doi: 10.1007/978-3-7091-8592-6_17.
Two patients with epilepsy and large hemispheric lesions underwent section of the frontal fibres of the corpus callosum for the treatment of seizures refractory to medical treatment. A severely retarded girl of 18 had encephalotrigeminal angiomatosis (Sturge-Weber syndrome) with multiple daily absences, tonic-clonic, myoclonic, atonic and adversive seizures since infancy. All types of fits--with the exception of adversive seizures and rare tonic-clonic fits--disappeared after anterior callosotomy. Another moderately retarded girl of 18 had an old cystic lesion over the entire territory of the left middle cerebral artery. She had had right hemiplegia since infancy and frequent brief absences and massive myoclonus triggered by unexpected sensory stimuli since the age of six years. Following anterior callosotomy there was an almost complete disappearance of the absences and a marked reduction of her startle myoclonus. Frontal callosotomy is a useful procedure in epileptics with large hemispheric lesions and carries less risk than hemispherectomy or total commissurotomy.
两名患有癫痫且有大脑半球大病灶的患者接受了胼胝体额叶纤维切断术,以治疗药物难治性癫痫发作。一名18岁的重度智障女孩患有脑三叉神经血管瘤病(斯特奇-韦伯综合征),自婴儿期起每天就有多次失神发作、强直阵挛发作、肌阵挛发作、失张力发作和偏转性发作。除了偏转性发作和罕见的强直阵挛发作外,所有类型的发作在进行胼胝体前部切开术后均消失。另一名18岁的中度智障女孩在左大脑中动脉的整个区域有一个陈旧性囊性病灶。她自婴儿期起就患有右侧偏瘫,自6岁起就频繁出现短暂失神发作,以及由意外感觉刺激引发的大量肌阵挛发作。在进行胼胝体前部切开术后,失神发作几乎完全消失,惊吓性肌阵挛明显减少。额叶胼胝体切开术对于患有大脑半球大病灶的癫痫患者是一种有用的手术,其风险比半球切除术或完全连合切开术要小。