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Inflammatory Demyelinating Central Nervous System Diseases in Childhood: Clinical and Paraclinical Profiles in 133 Patients

机译:儿童炎症性脱髓鞘中枢神经系统疾病:133例患者的临床和临床旁资料

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In a retrospective review of patients with acquired demyelinating disorders of the central nervous system, 133 patients (5.6%) whose diseases started in childhood, were selected from 2369 patients, who had medical records in the Neurology Department of Dokuz Eylul University. Out of 133, 98 had relapsing remitting multiple sclerosis, 21 had secondary progressive multiple sclerosis, 8 had clinically isolated syndrome, 3 had neuromyelitis optica, 2 had Marburg disease, and 1 had radiologically isolated syndrome. In 55 patients (41.3%), disease onset was before age 16. Polysymptomatic presentation (22.6%) was the most common initial feature. The EDSS scores ranged from 0 to 9 with a median of 2.0 (2.22±1.88) for 126 patients. MRI records of 111 patients were obtained. 97 patients had clinically definite multiple sclerosis. 11 MS patients (11.3%) did not initially present the diagnostic MRI features. All of the remaining multiple sclerosis patients fulfilled Barkhof-Tintore criteria (100%) and 88.7% fulfilled KIDMUS criteria. Cranial MRI of NMO patients was normal. Our findings demonstrate some important clinical and paraclinical features that can help the literature on acquired demyelinating disorders of childhood by utilizing data from Western Turkey.
机译:在对患有获得性中枢神经系统脱髓鞘疾病的患者进行的回顾性研究中,从2369位在杜库兹埃勒大学神经病学部门就诊的患者中选择了133例(5.6%)始于儿童期。在133例患者中,有98例患有复发性多发性硬化症,21例患有继发性进行性多发性硬化症,8例患有临床孤立综合征,3例患有视神经脊髓炎,2例患有马尔堡病,1例患有放射孤立综合征。在55例患者中(41.3%),该病发病于16岁之前。多症状表现(22.6%)是最常见的初始特征。 126名患者的EDSS评分范围为0至9,中位数为2.0(2.22±1.88)。获得111例患者的MRI记录。临床确诊的多发性硬化症97例。 11名MS患者(11.3%)最初并未表现出诊断性MRI特征。其余所有多发性硬化症患者均符合Barkhof-Tintore标准(100%),88.7%符合KIDMUS标准。 NMO患者的颅骨MRI正常。我们的发现证明了一些重要的临床和临床外特征,这些特征可以通过利用来自西土耳其的数据来帮助有关儿童获得性脱髓鞘疾病的文献。

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