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皮质发育畸形的影像学检查

Imaging of malformations of cortical development.

作者信息

Colombo Nadia, Salamon Noriko, Raybaud Charles, Ozkara Cigdem, Barkovich A James

机构信息

Department of Neuroradiology, Niguarda Ca' Granda Hospital, Milano, Italy.

出版信息

Epileptic Disord. 2009 Sep;11(3):194-205. doi: 10.1684/epd.2009.0262. Epub 2009 Sep 1.

Abstract

Malformations of cortical development (MCD) include a broad range of disorders that result from disruption of the major steps of cortical development: cell proliferation in germinal zones, neuronal migration and cortical organization. With the improvement and increased utilization of modern imaging techniques, MCD have been increasingly recognized as a major cause of seizure disorders. The advent of Magnetic Resonance Imaging (MRI), in particular, has revolutionized the investigation and the treatment of patients with epilepsy. High-resolution MRI may elucidate the type, the extension and the localization of MCD; therefore, in a group of patients suffering from drug-resistant partial epilepsy (DRPE), MRI greatly contributes to the identification of subjects who are suitable for surgical treatment. In the recent past, many efforts were addressed to establish the MRI diagnostic criteria for a peculiar group of MCD, namely focal cortical dysplasias (FCD), histopathologically distinguished as types I and II. Some subtle FCD, which were previously cryptic to imaging investigation, can now be recognized by MRI, however their detection and specification remains challenging. This review will re-visit the neuroimaging findings, including structural MRI, PET, co-registered PET/MRI, MEG and diffusion tensor imaging (DTI) of FCD types I and II. Three major issues will be discussed: 1) the morphological MRI features of the FCDs, 2) the utility of PET and MEG and the use of co-registration methods and 3) diffusion tensor imaging (DTI) as a future modality of investigation, which may add additional informations regarding the microstructure of the grey matter (GM) and white matter (WM) in cortical dysplasia.

摘要

皮质发育畸形(MCD)包括一系列由皮质发育主要步骤中断引起的疾病:生发区细胞增殖、神经元迁移和皮质组织形成。随着现代成像技术的改进和应用增加,MCD越来越被认为是癫痫发作障碍的主要原因。特别是磁共振成像(MRI)的出现,彻底改变了癫痫患者的检查和治疗方式。高分辨率MRI可以阐明MCD的类型、范围和定位;因此,在一组耐药性部分性癫痫(DRPE)患者中,MRI对确定适合手术治疗的患者有很大帮助。最近,人们做出了许多努力来建立一组特殊的MCD,即局灶性皮质发育不良(FCD)的MRI诊断标准,FCD在组织病理学上分为I型和II型。一些以前在影像学检查中难以发现的细微FCD现在可以通过MRI识别出来,然而它们的检测和特征描述仍然具有挑战性。本综述将重新审视I型和II型FCD的神经影像学表现,包括结构MRI、PET、联合注册PET/MRI、MEG和扩散张量成像(DTI)。将讨论三个主要问题:1)FCD的形态学MRI特征,2)PET和MEG的效用以及联合注册方法的使用,3)扩散张量成像(DTI)作为一种未来的检查方式,它可能会增加有关皮质发育异常中灰质(GM)和白质(WM)微观结构的额外信息。

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