Differentiation of neuromyelitis optica spectrum disorders from ultra-longitudinally extensive transverse myelitis in a cohort of Chinese patients

被引:3
作者
Zhang, Weihe [1 ]
Jiao, Yujuan [1 ]
Cui, Lei [1 ]
Jiao, Jinsong [1 ]
机构
[1] China Japan Friendship Hosp, Dept Neurol, 2 Yinghua, Beijing 100029, Peoples R China
关键词
Longitudinally extensive transverse myelitis; ultra; Neuromyelitis optica spectrum disorders; Causes; Clinical; Imaging; DIAGNOSTIC-CRITERIA; LESIONS;
D O I
10.1016/j.jneuroim.2016.01.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
This study aimed to differentiate neuromyelitis optica spectrum disorders (NMOSD) from other causes in cases of ultra-longitudinally extensive transverse myelitis (uLETM). We retrospectively analyzed thirty-three Chinese patients with uLETM hospitalized in the China-Japan Friendship Hospital. The patients were divided into NMOSD (n = 21) and non-NMOSD (n = 12) groups. The NMOSD group exhibited significantly more comorbidity compared with the non-NMOSD group; moreover, the NMOSD group uniquely exhibited intractable vomiting and hiccups (IVH). The prevalence rates of cervicothoracic, area postrema (AP), and other circumventricular organ (CVO) lesions were significantly increased in the NMOSD group compared with the non-NMOSD group. Moreover, uLETM was strongly associated with NMOSD. These novel findings indicate that CVO lesions, including AP, and particularly when combined with clinical IVH, may represent a useful discriminator to differentiate NMOSD. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:96 / 100
页数:5
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