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[多发性硬化症质子核磁共振成像的贡献。多自旋回波序列的贡献]

[Contribution to proton nuclear magnetic resonance imaging in multiple sclerosis. Contribution of a multiple spin echo sequence].

作者信息

Rumbach L, Caires M C, Warter J M, Collard M, Scheiber C, Gounot D, Dumitresco B, Chambron J

出版信息

Rev Neurol (Paris). 1985;141(8-9):583-6.

PMID:4089421
Abstract

Single or multiple parenchymatous anomalies were detected in 48 of 49 patients with multiple sclerosis by proton magnetic resonance imaging (MRI) combined with a spin-echo sequence in the 4 planes of the section passing through the ventricular bodies. Lesions were identified in the frontal, orbital and particularly juxta-ventricular white substance, and were of variable appearance, the most common being spots in the parenchyma and juxta-ventricular bands. A limited number of sections is sufficient for the MRI study of anomalies in clinically defined multiple sclerosis, the diagnostic value of this examination suggested by these findings requiring confirmation by prospective studies.

摘要

通过质子磁共振成像(MRI)结合自旋回波序列,在穿过脑室体的4个层面上,对49例多发性硬化症患者中的48例进行检查,发现了单发或多发的实质异常。病变见于额叶、眶叶,尤其是脑室周围白质,外观各异,最常见的是实质内斑点和脑室周围带。对于临床确诊的多发性硬化症,有限数量的切片足以进行异常情况的MRI研究,这些发现提示该检查的诊断价值有待前瞻性研究加以证实。

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[Contribution to proton nuclear magnetic resonance imaging in multiple sclerosis. Contribution of a multiple spin echo sequence].[多发性硬化症质子核磁共振成像的贡献。多自旋回波序列的贡献]
Rev Neurol (Paris). 1985;141(8-9):583-6.
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[Magnetic resonance imaging in multiple sclerosis. Sensitivity and correlation with the clinical picture].
Rev Neurol (Paris). 1986;142(6-7):598-606.
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Biochemical alterations in multiple sclerosis lesions and normal-appearing white matter detected by in vivo 31P and 1H spectroscopic imaging.通过体内31P和1H光谱成像检测多发性硬化症病变和外观正常的白质中的生化改变。
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Serial proton magnetic resonance spectroscopic imaging, contrast-enhanced magnetic resonance imaging, and quantitative lesion volumetry in multiple sclerosis.多发性硬化症中的系列质子磁共振波谱成像、对比增强磁共振成像及定量病变容积测定
Ann Neurol. 1998 Jan;43(1):56-71. doi: 10.1002/ana.410430112.

引用本文的文献

1
Relationship of nuclear magnetic resonance examinations to clinical data, cerebrospinal fluid findings and visual evoked potentials in multiple sclerosis.
Neurosurg Rev. 1987;10(3):201-8. doi: 10.1007/BF01782048.