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利用磁共振成像对胼胝体后天性病变进行分类。

Classification of acquired lesions of the corpus callosum with MRI.

作者信息

Friese S A, Bitzer M, Freudenstein D, Voigt K, Küker W

机构信息

Department of Neuroradiology, Eberhard-Karls-University, D-72074 Tübingen, Germany.

出版信息

Neuroradiology. 2000 Nov;42(11):795-802. doi: 10.1007/s002340000430.

Abstract

MRI has facilitated diagnostic assessment of the corpus callosum. Diagnostic classification of solitary or multiple lesions of the corpus callosum has not attracted much attention, although signal abnormalities are not uncommon. Our aim was to identify characteristic imaging features of lesions frequently encountered in practice. We reviewed the case histories of 59 patients with lesions shown on MRI. The nature of the lesions was based on clinical features and/or long term follow-up (ischaemic 20, Virchow-Robin spaces 3, diffuse axonal injury 7, multiple sclerosis 11, hydrocephalus 5, acute disseminated encephalomyelitis 5, Marchiafava-Bignami disease 4, lymphoma 2, glioblastoma hamartoma each 1). The location in the sagittal plane, the relationship to the borders of the corpus callosum and midline and the size were documented. The 20 ischaemic lesions were asymmetrical but adjacent to the midline; the latter was involved in new or large lesions. Diffuse axonal injury commonly resulted in large lesions, which tended to be asymmetrical; the midline and borders of the corpus callosum were always involved. Lesions in MS were small, at the lower border of the corpus callosum next to the septum pellucidum, and crossed the midline asymmetrically. Acute disseminated encephalomyelitis and the other perivenous inflammatory diseases caused relatively large, asymmetrical lesions. Hydrocephalus resulted in lesions of the upper part of the corpus callosum, and mostly in its posterior two thirds; they were found in the midline. Lesions in Marchiafava-Bignami disease were large, often symmetrically in the midline in the splenium and did not reach the edge of the corpus callosum.

摘要

磁共振成像(MRI)有助于胼胝体的诊断评估。尽管信号异常并不罕见,但胼胝体单发或多发病变的诊断分类并未引起太多关注。我们的目的是确定实践中常见病变的特征性影像学表现。我们回顾了59例MRI显示有病变患者的病历。病变的性质基于临床特征和/或长期随访结果(缺血性病变20例、血管周围间隙3例、弥漫性轴索损伤7例、多发性硬化11例、脑积水5例、急性播散性脑脊髓炎5例、马奇亚法瓦-比尼亚米病4例、淋巴瘤2例、胶质母细胞瘤错构瘤各1例)。记录了矢状面的位置、与胼胝体边界及中线的关系以及大小。20例缺血性病变不对称,但靠近中线;中线在新发病变或大病变中受累。弥漫性轴索损伤通常导致大病变,且往往不对称;胼胝体的中线和边界总是受累。多发性硬化症的病变较小,位于胼胝体靠近透明隔的下缘,并不对称地穿过中线。急性播散性脑脊髓炎和其他静脉周围炎性疾病导致相对较大的不对称病变。脑积水导致胼胝体上部出现病变,且大多位于其后三分之二;病变位于中线。马奇亚法瓦-比尼亚米病的病变较大,通常对称位于胼胝体压部的中线,且未到达胼胝体边缘。

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