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皮质发育畸形中海马异常的模式。

Patterns of hippocampal abnormalities in malformations of cortical development.

作者信息

Montenegro M A, Kinay D, Cendes F, Bernasconi A, Bernasconi N, Coan A C, Li L M, Guerreiro M M, Guerreiro C A M, Lopes-Cendes I, Andermann E, Dubeau F, Andermann F

机构信息

Department of Neurology, University of Campinas/FCM-UNICAMP, Campinas, SP, Brazil.

出版信息

J Neurol Neurosurg Psychiatry. 2006 Mar;77(3):367-71. doi: 10.1136/jnnp.2005.070417.

Abstract

OBJECTIVE

To assess whether different types of malformation of cortical development (MCD) are associated with specific patterns of hippocampal abnormalities.

METHODS

A total of 122 consecutive patients with MRI diagnosis of MCD (53 males, age range 1-58 years) were included in the study. Hippocampal measurements were made on 1-3 mm coronal T1-weighted MRIs and compared with MRIs of normal controls.

RESULTS

A total of 39 patients had focal cortical dysplasia, 5 had hemimegalencephaly, 5 had lissencephaly-agyria-pachygyria, 11 had SLH, 11 had PNH, 12 had bilateral contiguous PNH, 5 had schizencephaly, and 34 had polymicrogyria. The frequency of hippocampal abnormalities in these patients with MCD was 29.5%. A small hippocampus was present in all types of MCD. Only patients with lissencephaly and SLH had an enlarged hippocampus. Abnormalities in hippocampal rotation and shape were present in all types of MCD; however, these predominated in PNH. None of the patients with lissencephaly-agyria-pachygyria or SLH had hyperintense signal on T2 or FLAIR images or abnormal hippocampal internal architecture.

CONCLUSION

A small hippocampus was present in all types of MCD; however, the classic MRI characteristics of hippocampal sclerosis were often lacking. Abnormal enlargement of the hippocampus was associated with only diffuse MCD due to abnormal neuronal migration (lissencephaly-agyria-pachygyria and SLH).

摘要

目的

评估不同类型的皮质发育畸形(MCD)是否与海马异常的特定模式相关。

方法

本研究纳入了122例经MRI诊断为MCD的连续患者(53例男性,年龄范围1 - 58岁)。在1 - 3毫米的冠状位T1加权MRI上进行海马测量,并与正常对照的MRI进行比较。

结果

共有39例患者患有局灶性皮质发育不良,5例患有半侧巨脑症,5例患有无脑回 - agyria - 巨脑回畸形,11例患有局灶性皮质下异位,11例患有多小脑回,12例患有双侧连续多小脑回,5例患有脑裂畸形,34例患有多微脑回。这些MCD患者中海马异常的发生率为29.5%。所有类型的MCD均存在海马体积小的情况。只有无脑回畸形和局灶性皮质下异位的患者海马体积增大。所有类型的MCD均存在海马旋转和形态异常;然而,这些异常在多小脑回中更为突出。无脑回 - agyria - 巨脑回畸形或局灶性皮质下异位的患者在T2或FLAIR图像上均无高信号或海马内部结构异常。

结论

所有类型的MCD均存在海马体积小的情况;然而,常常缺乏海马硬化的典型MRI特征。海马异常增大仅与神经元迁移异常导致的弥漫性MCD(无脑回 - agyria - 巨脑回畸形和局灶性皮质下异位)相关。

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