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在早期帕金森病为主的多系统萎缩症的 3-T 磁共振成像上的豆状核异常。

Putaminal abnormality on 3-T magnetic resonance imaging in early parkinsonism-predominant multiple system atrophy.

机构信息

Department of Neurology, Seoul National University Boramae Hospital, Seoul, Korea.

出版信息

J Neurol. 2010 Dec;257(12):2065-70. doi: 10.1007/s00415-010-5661-x. Epub 2010 Jul 22.

Abstract

To evaluate the diagnostic value of putaminal abnormality on 3-T magnetic resonance imaging (MRI) for differentiating early parkinsonism-predominant multiple system atrophy (MSA-p) from Parkinson disease (PD) based on long-term clinical follow-up data. Totals of 23 clinical MSA-p (6 possible and 17 suspicious) and 50 PD patients were included. Subjects submitted to 3-T MRI at baseline and were followed up to substantiate the initial diagnosis. MRI findings were compared between MSA-p and PD patients based on the final diagnosis. Putaminal abnormalities were recorded as presence of atrophy, signal hypointensity, and abnormal disruption of the hyperintense lateral rim of the putamen. The sum scores for putaminal abnormality were calculated from the presence of each item. During the follow-up over 3 years, the diagnosis of MSA-p was supported in 17 patients (14 probable and 3 possible) and the diagnosis of PD was stable in all 50 patients. Putaminal abnormalities were more frequent in MSA-p (n = 17) than in PD (n = 50). A sum score of >1 on 3-T MRI had sensitivity, specificity, and positive- and negative-predictive values of 70.6, 93, 77.4, and 90.3%, respectively, for differentiating MSA-p from PD. Fourteen of the initial 23 clinical MSA-p patients had a sum score of >1, and in all but two, the diagnosis became supported during the follow-up, whereas the diagnosis of five of the nine patients with a sum score of ≤1 remained uncertain. Putaminal abnormality on 3-T MRI can be a specific diagnostic marker for early stage MSA-p.

摘要

为了评估在 3T 磁共振成像(MRI)上纹状体异常对基于长期临床随访数据区分早期以帕金森病为主的多系统萎缩(MSA-p)与帕金森病(PD)的诊断价值。共纳入 23 例临床 MSA-p(6 例可能,17 例可疑)和 50 例 PD 患者。所有患者均在基线时进行 3T MRI 检查,并随访以证实初始诊断。根据最终诊断比较 MSA-p 和 PD 患者的 MRI 结果。纹状体异常记录为萎缩、信号低信号和纹状体高信号外侧缘异常中断。从每项存在的情况计算纹状体异常的总分。在 3 年的随访期间,17 例患者(14 例可能,3 例可疑)支持 MSA-p 的诊断,而 50 例患者的 PD 诊断均稳定。与 PD(n=50)相比,MSA-p(n=17)的纹状体异常更为常见。3T MRI 上总分>1 对区分 MSA-p 和 PD 的敏感性、特异性、阳性预测值和阴性预测值分别为 70.6%、93%、77.4%和 90.3%。23 例初始临床 MSA-p 患者中有 14 例的总分>1,除 2 例外,所有患者的诊断在随访期间得到支持,而 9 例总分≤1 的患者中有 5 例的诊断仍不确定。3T MRI 上的纹状体异常可能是早期 MSA-p 的特异性诊断标志物。

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