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患有广泛性囊肿性脑白质软化症婴儿的神经学、电生理学及磁共振成像异常

Neurological, electrophysiological and MRI abnormalities in infants with extensive cystic leukomalacia.

作者信息

De Vries L S, Connell J A, Dubowitz L M, Oozeer R C, Dubowitz V, Pennock J M

出版信息

Neuropediatrics. 1987 May;18(2):61-6. doi: 10.1055/s-2008-1052453.

Abstract

Twenty infants, diagnosed by cranial ultrasound as having extensive cystic leukomalacia, had visual evoked responses (VER) and electroencephalograms (EEG) in the neonatal period and MRI scans later in infancy. The early ultrasound findings and results from the electrophysiological tests were correlated with later MRI findings and functional abilities. In infants with periventricular leukomalacia (PVL), the cysts were usually no longer visible by ultrasonography, beyond 40 weeks postmenstrual age (PMA), but later MRI scans showed a consistent pattern of delayed myelination around the irregularly dilated occipital horns of the lateral ventricles. VER's were present in the neonatal period and vision was maintained, although all infants developed a marked squint. EEG's were either normal or abnormal initially, but improvement was noted within several weeks. In those with subcortical or mixed lesions, cysts were noted to persist beyond 40 weeks PMA. Later MRI scans showed very poor myelination, with poor progress on subsequent scans and cortical atrophy. VER's were absent and all infants later became cortically blind. EEG's were severely abnormal and recovery was very poor. The infants with PVL developed spastic diplegia with moderate developmental delay, while those with mixed or subcortical lesions developed quadriplegia with severe mental retardation. An integrated approach, consisting of ultrasound imaging and electrophysiological recordings in the neonatal period and MRI imaging later in infancy, may provide a more reliable prediction of the pattern of later deficits.

摘要

二十名经头颅超声诊断为广泛囊性脑白质软化的婴儿,在新生儿期进行了视觉诱发电位(VER)和脑电图(EEG)检查,并在婴儿期后期进行了磁共振成像(MRI)扫描。早期超声检查结果和电生理测试结果与后期MRI检查结果及功能能力相关。在患有脑室周围白质软化(PVL)的婴儿中,囊肿通常在孕龄40周后超声检查时不再可见,但后期MRI扫描显示,侧脑室枕角不规则扩张周围存在一致的髓鞘延迟形成模式。新生儿期存在VER且视力得以维持,尽管所有婴儿都出现了明显的斜视。EEG最初正常或异常,但在数周内有所改善。在患有皮质下或混合性病变的婴儿中,囊肿在孕龄40周后仍持续存在。后期MRI扫描显示髓鞘形成极差,后续扫描进展不佳且出现皮质萎缩。VER缺失,所有婴儿后来均出现皮质盲。EEG严重异常且恢复很差。患有PVL的婴儿发展为痉挛性双瘫,伴有中度发育迟缓,而患有混合性或皮质下病变的婴儿则发展为四肢瘫,伴有严重智力迟钝。一种综合方法,包括新生儿期的超声成像和电生理记录以及婴儿期后期的MRI成像,可能会为后期缺陷模式提供更可靠的预测。

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