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7T MRI 显示出不同的病变形态,可将视神经脊髓炎与多发性硬化区分开来。

Distinct lesion morphology at 7-T MRI differentiates neuromyelitis optica from multiple sclerosis.

机构信息

NeuroCure Clinical Research Center, Charité-Universitaetsmedizin Berlin, Berlin, Germany.

出版信息

Neurology. 2012 Aug 14;79(7):708-14. doi: 10.1212/WNL.0b013e3182648bc8. Epub 2012 Aug 1.

Abstract

OBJECTIVE

To investigate distinct white matter and cortical gray matter pathology in neuromyelitis optica spectrum disorders (NMOSDs) and multiple sclerosis (MS) at 7-T MRI in a cross-sectional study.

METHODS

We included 10 patients with NMOSDs and 18 patients with MS in our 7-T MRI study. The imaging protocol comprised T2*-weighted fast low angle shot and turbo inversion recovery magnitude sequences. White matter and cortical gray matter lesions were assessed with special regard to their (perivascular) localization as well as the expression of a hypointense rim.

RESULTS

In total, we detected 140 white matter lesions in 7 of 10 patients with NMOSDs. In contrast to MS plaques, which were nearly exclusively centered by a small vein (92%) and showed a characteristic hypointense rim (23%), white matter changes in patients with NMOSDs were nonspecific in appearance and were only infrequently neighbored by a blood vessel (49 lesions [35%], p = 0.003). Hypointense rims were very rarely detectable (3 lesions [2%], p < 0.001). Cortical pathology was absent in NMOSDs. In our MS cohort, we detected 36 leukocortical, 8 intracortical, and 8 subpial cortical lesions in 7 of 18 patients.

CONCLUSION

The MRI features of white matter and the absence of cortical gray matter findings substantially differentiate NMOSDs from MS and can be used as a potential marker to distinguish these 2 entities. The fact that cortical pathology is common in MS but is not present in patients with NMOSDs may reflect the difference in the underlying pathogenesis.

摘要

目的

在横断面研究中,通过 7-T MRI 研究来探究视神经脊髓炎谱系障碍(NMOSD)和多发性硬化(MS)患者之间明显的白质和皮质灰质病理学差异。

方法

我们纳入了 10 名 NMOSD 患者和 18 名 MS 患者进行 7-T MRI 研究。该成像方案包括 T2*-加权快速小角度激发和涡轮反转恢复幅度序列。白质和皮质灰质病变是通过血管周围定位以及低信号边缘的表达来评估的。

结果

我们在 7 名 NMOSD 患者中总共检测到 140 个白质病变。与 MS 斑块不同,后者几乎完全由小静脉(92%)中心,并表现出特征性的低信号边缘(23%),NMOSD 患者的白质病变表现为非特异性,很少与血管相邻(49 个病变[35%],p=0.003)。低信号边缘非常罕见(3 个病变[2%],p<0.001)。NMOSD 中不存在皮质病变。在我们的 MS 队列中,在 7 名患者中检测到 36 个白质皮质、8 个皮质内和 8 个皮质下皮质病变。

结论

白质的 MRI 特征和皮质灰质病变的缺失可将 NMOSD 与 MS 明显区分开来,可作为区分这两种疾病的潜在标志物。皮质病变在 MS 中很常见,但在 NMOSD 患者中不存在,这可能反映了两种疾病在发病机制上的差异。

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