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病理白质中长T2水的磁共振成像证据。

MR evidence of long T2 water in pathological white matter.

作者信息

Laule Cornelia, Vavasour Irene M, Mädler Burkhard, Kolind Shannon H, Sirrs Sandra M, Brief Elana E, Traboulsee Anthony L, Moore G R Wayne, Li David K B, MacKay Alex L

机构信息

Department of Radiology, University of British Columbia, Vancouver, BC, Canada.

出版信息

J Magn Reson Imaging. 2007 Oct;26(4):1117-21. doi: 10.1002/jmri.21132.

Abstract

PURPOSE

To describe what, if any, specific long T(2)-related abnormalities occur in the white matter of subjects with either phenylketonuria (PKU) or multiple sclerosis (MS).

MATERIALS AND METHODS

The 48-echo T(2) relaxation data (maximum TE = 1.12 sec) were acquired from 15 PKU subjects, 20 MS subjects, and 15 healthy volunteers. Regions of interest were drawn in diffuse white matter hyperintensities (DiffWM), lesions, normal-appearing white matter (NAWM), and normal white matter. Long T(2) maps (200 msec < T(2) < 800 msec) were created for each subject.

RESULTS

A new water reservoir with a markedly prolonged T(2) peak was identified in DiffWM and NAWM in 12 out of 15 subjects with PKU and a long T(2) signal was also seen in 23/97 lesions in 50% of subjects with MS. Additionally, a long T(2) component was observed in the corticospinal tracts of 10 healthy volunteers. The characteristics of the long T(2) signal were unique for each subject group. Potential sources of this signal include vacuolation and increases in extracellular water.

CONCLUSION

This study supports the usefulness of increasing the data acquisition window of the multiecho T(2) relaxation sequence to better characterize the T(2) decay from pathological brain.

摘要

目的

描述苯丙酮尿症(PKU)或多发性硬化症(MS)患者白质中是否存在与长T(2)相关的特定异常。

材料与方法

从15名PKU患者、20名MS患者和15名健康志愿者获取48回波T(2)弛豫数据(最大TE = 1.12秒)。在弥漫性白质高信号(DiffWM)、病变、正常白质(NAWM)和正常白质中绘制感兴趣区域。为每位受试者创建长T(2)图(200毫秒 < T(2) < 800毫秒)。

结果

在15名PKU患者中的12名患者的DiffWM和NAWM中发现了一个新的水储备池,其T(2)峰值明显延长,并且在50%的MS患者的23/97个病变中也观察到长T(2)信号。此外,在10名健康志愿者的皮质脊髓束中观察到长T(2)成分。每个受试者组的长T(2)信号特征都是独特的。该信号的潜在来源包括空泡化和细胞外水增加。

结论

本研究支持增加多回波T(2)弛豫序列的数据采集窗口以更好地表征病理性脑T(2)衰减的有用性。

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