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MRI上的“双皮质”综合征

The 'double cortex' syndrome on MRI.

作者信息

Hashimoto R, Seki T, Takuma Y, Suzuki N

机构信息

Department of Pediatrics, Shizuoka Red Cross Hospital, Japan.

出版信息

Brain Dev. 1993 Jan-Feb;15(1):57-9; discussion 83-4. doi: 10.1016/0387-7604(93)90007-u.

Abstract

We report a 6-year-old girl with diffuse subcortical heterotopia (band heterotopia), an unusual type of ectopic gray matter on magnetic resonance imaging (MRI). Her cerebral parenchyma had four layers consisting of cortex, thin outer white matter, diffuse subcortical heterotopia, and inner white matter around the lateral ventricles, giving the appearance of a 'double cortex'. The overlying cortex had midly broad gyri, especially in the frontal lobes. MRI showed the appearance of laminar heterotopia, a classical pathological entity. The double cortex syndrome is presumably a radiological delineation of laminar heterotopia. Her development was slightly delayed and she was clumsy and easily upset, with poor impulse control. However, her daily life was largely unaffected in spite of the severe abnormalities on MRI. She had abnormal movements during sleep, and sleeping EEG showed high voltage spindles in the bilateral frontal areas but no epileptic discharges. It could not be determined whether or not these movements were epileptic. The double cortex syndrome, an anomaly of the central nervous system associated with mental retardation, epilepsy, behavioral problems, and exclusive occurrence in girls, will be established as a clinico-radiological entity.

摘要

我们报告了一名6岁女孩,患有弥漫性皮质下异位(带状异位),这是一种在磁共振成像(MRI)上表现为异常类型的异位灰质。她的脑实质有四层结构,由皮质、薄的外层白质、弥漫性皮质下异位以及围绕侧脑室的内层白质组成,呈现出“双皮质”的外观。上方的皮质有轻度宽阔的脑回,尤其是在额叶。MRI显示出层状异位的表现,这是一种典型的病理实体。双皮质综合征可能是层状异位的一种影像学描述。她的发育稍有延迟,动作笨拙,容易烦躁,冲动控制能力差。然而,尽管MRI显示有严重异常,但她的日常生活基本未受影响。她在睡眠期间有异常动作,睡眠脑电图显示双侧额叶区域有高电压纺锤波,但无癫痫放电。无法确定这些动作是否为癫痫发作。双皮质综合征是一种与智力发育迟缓、癫痫、行为问题相关的中枢神经系统异常,且仅见于女孩,将被确立为一种临床影像学实体。

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