Guerrini R, Dravet C, Raybaud C, Roger J, Bureau M, Battaglia A, Livet M O, Colicchio G, Robain O
INPE University of Pisa-IRCCS Stella Maris, Italy.
Dev Med Child Neurol. 1992 Aug;34(8):694-705. doi: 10.1111/j.1469-8749.1992.tb11505.x.
The authors studied 10 patients aged between six and 23 years (mean age 14 years 5 months) with magnetic resonance imaging, which detected bilateral 'macrogyric-like' maldevelopment of the insulo-opercular regions. The data confirm that biopercular gyral anomaly, associated with mental retardation, pseudobulbar palsy (cortical or central) and epilepsy, represents an anatomo-clinical syndrome. Nevertheless, a wide clinical spectrum was found varying from pictures correlating with the topography and extent of the MRI-detected anomaly to conditions indicating wider cerebral involvement. Epilepsy, varying greatly in age at onset and severity, consistently influenced the prognosis for five patients with diffuse EEG abnormalities and intractable seizures with falls. Anterior callosotomy relieved such seizures in one case.
作者对10名年龄在6岁至23岁之间(平均年龄14岁5个月)的患者进行了磁共振成像研究,该研究检测到岛盖区双侧“巨脑回样”发育异常。数据证实,与智力发育迟缓、假性延髓麻痹(皮质或中枢性)和癫痫相关的双岛盖脑回异常代表一种解剖学-临床综合征。然而,发现了广泛的临床谱,从与MRI检测到的异常的部位和范围相关的表现到提示更广泛脑受累的情况不等。癫痫的起病年龄和严重程度差异很大,持续影响着5名脑电图弥漫性异常且有跌倒发作的难治性癫痫患者的预后。在1例患者中,前胼胝体切开术缓解了此类癫痫发作。