Takeuchi Y, Matsushita H, Yamazoe I, Nagai H, Takaya K, Fujiwara F, Sawada T
Department of Pediatrics, Kyoto Prefectural University of Medicine, Japan.
Pediatr Neurol. 1998 Jul;19(1):26-30. doi: 10.1016/s0887-8994(98)00007-1.
A clinical study of 15 patients without underlying disorders whose first seizures occurred before 1 year of age was performed to determine the characteristics of localization-related epilepsies in infancy. The patients were retrospectively divided into two groups: the seizure-controlled group (10 patients) and the refractory group (five patients). The seizure-controlled group included patients whose seizures were controlled completely within 1 year after onset; the refractory group included all other patients. The characteristics of the refractory group were as follows: (1) interictal electroencephalography showed focal abnormalities, particularly on the left side, and (2) all of the patients exhibited developmental retardation. Even in the seizure-controlled group, 40% of the patients exhibited developmental retardation, and all of them were indistinguishable from patients with benign complex partial epilepsies in infancy at the onset of the seizures. Aggressive treatment should be re-evaluated for early-onset localization-related epilepsies.
对15例无潜在疾病且首次发作发生在1岁之前的患者进行了一项临床研究,以确定婴儿期局灶性相关性癫痫的特征。这些患者被回顾性地分为两组:癫痫发作得到控制的组(10例患者)和难治性组(5例患者)。癫痫发作得到控制的组包括那些发作后1年内癫痫发作完全得到控制的患者;难治性组包括所有其他患者。难治性组的特征如下:(1)发作间期脑电图显示局灶性异常,特别是在左侧,以及(2)所有患者均表现出发育迟缓。即使在癫痫发作得到控制的组中,40%的患者也表现出发育迟缓,并且在癫痫发作开始时,他们所有人与婴儿期良性复杂部分性癫痫患者无法区分。对于早发性局灶性相关性癫痫,应重新评估积极治疗。