The pathologic and diagnostic in magnetic resonance imaging of brain and cervical spine of patients with neuromyelitis optica spectrum disorder.

Iranian Journal of Neurology Pub Date : 2018-04-04
Roshanak Mehdipour-Dastjerdi, Fereshteh Ashtari, Vahid Shaygannejad, Marjan Mansourian, Ali Safaei
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Abstract

Background: Neuromyelitis optica spectrum disease (NMOSD) is a chronic inflammatory demyelinating disorder that involves central nervous system (CNS) with high affinity for involvement of optic nerve and spinal cord. In current study, due to high prevalence of NMOSD in Isfahan, Iran, we have aimed to assess brain and spine magnetic resonance imaging (MRI) of patients with NMOSD. Methods: This cross-sectional study was performed on 62 patients with diagnosis of NMOSD, who referred to MS clinic of Kashani hospital, Isfahan City, during 2015-17. Patients' age, age of onset, primary brain and spine MRI findings, and expanded disability status scale (EDSS) were recorded in check list. Patients underwent new brain and spine MRI. Data were analyzed with SPSS software. Descriptive data were reported by mean ± standard deviation (SD). Results: 62 known cases of NMOSD including 9 (14.5%) men and 53 (85.5%) women with mean age of 34.32 ± 10.26 years, mean age of onset of 28.03 ± 12.09 years, and mean EDSS of 2.63 ± 1.55 were assessed. 33.9% of patients were anti-neuromyelitis optica (NMO) antibody seropositive. Longitudinal extensive transverse myelitis (LETM) and segmental spinal lesions were found in 66.1% and 29.0% of patients, respectively. Diagnostic NMO brain lesions and posterior periventricular lesions were seen in 38.7% and 67.7% of patients, respectively. Two patients had tumefactive lesions. Conclusion: In current study, we found high rate of posterior periventricular lesions in brain MRI and segmental lesions in spine MRI of both anti-NMO antibody seropositive and seronegative patients. As these lesions are not in NMOSD diagnosis criteria, more considerations are recommended. In addition, tumefactive lesions in patients with NMOSD were an exciting finding of this study that should be discussed about more.

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视神经脊髓炎频谱障碍患者脑、颈椎磁共振成像的病理与诊断。
背景:视神经脊髓炎(NMOSD)是一种累及中枢神经系统(CNS)的慢性炎症性脱髓鞘疾病,对视神经和脊髓具有高度亲和性。在本研究中,由于NMOSD在伊朗伊斯法罕的高患病率,我们旨在评估NMOSD患者的脑和脊柱磁共振成像(MRI)。方法:对2015- 2017年在伊斯法罕市Kashani医院MS门诊就诊的62例诊断为NMOSD的患者进行横断面研究。检查表中记录患者年龄、发病年龄、颅脑及脊柱MRI原发表现、扩展失能状态量表(EDSS)。患者接受新的脑部和脊柱MRI检查。数据采用SPSS软件进行分析。描述性数据以均数±标准差(SD)报告。结果:已知NMOSD 62例,其中男性9例(14.5%),女性53例(85.5%),平均年龄34.32±10.26岁,平均发病年龄28.03±12.09岁,平均EDSS 2.63±1.55。33.9%的患者抗视神经脊髓炎(NMO)抗体血清阳性。纵向广泛横脊髓炎(LETM)和节段性脊柱病变分别占66.1%和29.0%。诊断性NMO脑病变和后脑室周围病变分别见于38.7%和67.7%的患者。2例患者有肿瘤病变。结论:在目前的研究中,我们发现抗nmo抗体血清阳性和血清阴性患者的脑MRI和脊柱MRI均有较高的后脑室周围病变发生率。由于这些病变不在NMOSD的诊断标准中,建议更多的考虑。此外,NMOSD患者的肿瘤病变是本研究的一个令人兴奋的发现,应该进行更多的讨论。
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来源期刊
Iranian Journal of Neurology
Iranian Journal of Neurology CLINICAL NEUROLOGY-
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