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首页> 外文期刊>Japanese Journal of Ophthalmology >Idiopathic third and sixth cranial nerve neuritis
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Idiopathic third and sixth cranial nerve neuritis

机译:特发性第三和第六次颅神经神经炎

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PurposeTo present cases with idiopathic third and sixth cranial nerve neuritis.Study designRetrospective observational studyMethodsThe results of high resolution pre- and post- cranial nerve magnetic resonance images (MRI) with three-dimensional sequences for visualizing cranial nerves in patients with third, fourth, and sixth cranial nerve palsies who were treated at the Neuro-ophthalmology Department of Samsung Medical Center were reviewed. Patients with cranial nerve enhancement confirmed by experienced radiologists were identified. The medical records of these patients were reviewed, and their demographics, clinical presentations, laboratory results, and clinical outcomes were analyzed.ResultsOf 265 patients with third, fourth, and sixth cranial nerve palsy, 60 were identified by high resolution MRI as having enhancement of the corresponding cranial nerve. Among these, 17 patients with infiltrative, granulomatous, or tumorous lesions were excluded. In addition, 28 patients with identifiable causes of cranial nerve palsy, such as Miller-fisher syndrome, virus infection, or radiation-induced neuropathy, as well as patients with vasculopathic risk factors, were also excluded. Ultimately, a total of 15 patients with idiopathic third and sixth cranial nerve neuritis were included in this study. The mean age of these patients was 43 15 years. Eight patients had sixth cranial nerve palsy, six third cranial nerve palsy (two partial and four complete), and one patient with complete third and sixth cranial nerve palsy. Nine patients received steroid treatment. Eleven patients recovered fully within a period ranging from a few days to one year. Two patients were much improved up to 1month after initial presentation, but were then ultimately lost to follow-up. Another patient was lost to follow-up after the initial work-up. The other patient lost to follow-up had partially recovered during the first 6months.ConclusionsWe present patients with idiopathic third and sixth cranial nerve neuritis. They tended to respond well to steroid treatment and to have good prognoses. In order to better understand the long-term prognosis of cranial nerve neuritis and possible association with other neurologic disorders, a larger scale and longer-term study is needed.
机译:有特发性第三和第六颅神经神经炎的purposeto现有病例。研究了高分辨率和颅神经磁共振图像(MRI)的高分辨率和颅神经磁共振图像(MRI)的结果,用于在第三,第四,第四个和患者中可视化颅神经的三维序列综述了在三星医疗中心神经眼科部门治疗的第六颅神经麻痹。鉴定了经验丰富的放射科学医生证实的颅神经增强患者。审查了这些患者的病历,分析了他们的人口统计,临床介绍,实验室结果和临床结果。通过高分辨率MRI确定了265名患有第三,第四和第六次颅神经麻痹,60名患者的患者相应的颅神经。其中,排除了17例渗透,肉芽肿或肿瘤病变。此外,还排除了28例颅神经麻痹的可识别原因,如米勒 - Fisher综合征,病毒感染或辐射诱导的神经病变,以及血管病患风险因素的患者。最终,本研究中共有15例特发性第三和第六颅神经神经炎患者。这些患者的平均年龄为43岁。八名患者患有六个颅神经麻痹,六个第三颅神经麻痹(两个部分和四个完整),一名患者完整的第三和第六次颅神经麻痹。九名患者接受类固醇治疗。 11名患者在几天至一年的时间内完全恢复。在初始介绍后,两名患者在初始化后达1个患者,但最终损失了随访。在初始化后,另一位患者失去了随访。在前6个月期间,其他患者失去了随访的患者已经部分地回收。结论治疗特发性第三和第六颅神经神经炎的患者。他们倾向于对类固醇治疗响应并具有良好的预测。为了更好地了解颅神经性神经炎的长期预后和与其他神经系统疾病的可能结合,需要更大的规模和长期研究。

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