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1 型神经纤维瘤病患者基底节和丘脑的质子磁共振波谱成像:与 T2 高信号的相关性。

Proton MR spectroscopic imaging of basal ganglia and thalamus in neurofibromatosis type 1: correlation with T2 hyperintensities.

机构信息

Department of Neuroradiology, CHRU & Tours University, Tours 37000, France.

出版信息

Neuroradiology. 2011 Feb;53(2):141-8. doi: 10.1007/s00234-010-0776-4. Epub 2010 Oct 20.

Abstract

INTRODUCTION

Neurofibromatosis type 1 (NF1) is frequently associated with hyperintense lesions on T2-weighted images called "unidentified bright objects" (UBO). To better characterize the functional significance of UBO, we investigate the basal ganglia and thalamus using spectroscopic imaging in children with NF1 and compare the results to anomalies observed on T2-weighted images.

METHODS

Magnetic resonance (MR) data of 25 children with NF1 were analyzed. On the basis of T2-weighted images analysis, two groups were identified: one with normal MR imaging (UBO- group; n = 10) and one with UBO (UBO+ group; n = 15). Within the UBO+ group, a subpopulation of patients (n = 5) only had lesions of the basal ganglia. We analyzed herein seven regions of interest (ROIs) for each side: caudate nucleus, capsulo-lenticular region, lateral and posterior thalamus, thalamus (lateral and posterior voxels combined), putamen, and striatum. For each ROI, a spectrum of the metabolites and their ratio was obtained.

RESULTS

Patients with abnormalities on T2-weighted images had significantly lower NAA/Cr, NAA/Cho, and NAA/mI ratios in the lateral right thalamus compared with patients with normal T2. These abnormal spectroscopic findings were not observed in capsulo-lenticular regions that had UBO but in the thalamus region that was devoid of UBO.

CONCLUSION

Multivoxel spectroscopic imaging using short-time echo showed spectroscopic abnormalities in the right thalamus of NF1 patients harboring UBO, which were mainly located in the basal ganglia. This finding could reflect the anatomical and functional interactions of these regions.

摘要

简介

神经纤维瘤病 1 型(NF1)常伴有 T2 加权图像上称为“未识别亮物体”(UBO)的高信号病变。为了更好地描述 UBO 的功能意义,我们使用磁共振波谱成像研究 NF1 患儿的基底节和丘脑,并将结果与 T2 加权图像上观察到的异常进行比较。

方法

对 25 例 NF1 患儿的磁共振(MR)数据进行分析。根据 T2 加权图像分析,将两组患儿进行区分:一组 MR 成像正常(UBO-组;n=10),另一组存在 UBO(UBO+组;n=15)。在 UBO+组中,亚组患者(n=5)仅存在基底节病变。我们分析了每侧 7 个感兴趣区(ROI):尾状核、壳核-苍白球区、外侧和后丘脑、丘脑(外侧和后区的体素组合)、壳核和纹状体。对每个 ROI,获得了代谢物及其比值的谱图。

结果

与 T2 正常的患者相比,T2 加权图像异常的患者右侧外侧丘脑的 NAA/Cr、NAA/Cho 和 NAA/mI 比值显著降低。这些异常的波谱发现不仅见于有 UBO 的壳核-苍白球区,也见于无 UBO 的丘脑区。

结论

使用短回波时间多体素磁共振波谱成像显示 NF1 伴 UBO 患者右侧丘脑存在波谱异常,主要位于基底节区。这一发现可能反映了这些区域的解剖和功能相互作用。

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