Aissa A, Ben Lassoued M, Alouini R
Service d'imagerie médicale, hôpital Ibn El Jazzar, rue Ibn El Jazzar, Al-Qayrawan, 3100 Kairouan, Tunisie.
Rev Neurol (Paris). 2013 Mar;169(3):223-7. doi: 10.1016/j.neurol.2012.11.002. Epub 2013 Feb 19.
Various etiologic diagnoses are put forward for certain forms of infant epilepsy. We report four cases illustrating a rare cause: gray matter heterotopia. There were three girls and one boy, aged 3 months to 4 years at onset of seizures and 8 to 30 years at diagnosis of gray matter heterotopia. All patients sought healthcare because of repeated seizures. One patient also presented severe mental retardation. No consanguinity was noted. Magnetic resonance imaging showed the interposition of an ectopic ribbon of gray matter within the white matter in all cases. Ectopic gray matter formed bilateral subependymal nodules in one patient and bilateral nodules in the subcortical region suggestive of concentric laminar organization in another. The two other patients presented both of these forms. Other anomalies were associated: partial agenesis of the corpus callosum associated with colpocephaly causing cortical atrophy in one patient and hippocampal sclerosis in another.
针对某些形式的婴儿癫痫提出了各种病因诊断。我们报告了4例病例,说明了一种罕见病因:灰质异位症。有3名女孩和1名男孩,癫痫发作起病时年龄为3个月至4岁,诊断为灰质异位症时年龄为8至30岁。所有患者均因反复癫痫发作而寻求医疗护理。1例患者还伴有严重智力发育迟缓。未发现近亲结婚情况。磁共振成像显示,所有病例中均有异位灰质带插入白质内。1例患者的异位灰质形成双侧室管膜下结节,另1例患者的异位灰质在皮质下区域形成双侧结节,提示同心层状结构。另外2例患者同时出现这两种形式。还伴有其他异常情况:1例患者胼胝体部分发育不全伴脑室扩大导致皮质萎缩,另1例患者伴有海马硬化。