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首页> 外文期刊>Neuro-ophthalmology >Horner Syndrome in a Case of Neuromyeiitis Optica
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Horner Syndrome in a Case of Neuromyeiitis Optica

机译:视神经脊髓炎病例中的霍纳综合征

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A 58-year-old right-handed woman presented with neck pain and right hemibody decreased pain and temperature sensation. Over the next 3 days, she developed left ptosis and miosis. The Horner syndrome was confirmed with 0.5% apraclonidine and neuromyeiitis optica immunoglobulin G antibody titres were positive. Magnetic resonance imaging of the cervical spine showed a longitudinally extensive intramedullary expansile lesion more prominent on the left, with post-contrast enhancement extending from C2 to C5, consistent with neuromyeiitis optica. This patient was diagnosed with neuromyeiitis optica with an associated left Horner syndrome.
机译:一名58岁的惯用右手的女人表现出颈部疼痛和右半身症状,减轻了疼痛并减轻了温度感。在接下来的三天内,她出现了左上睑下垂和瞳孔缩小。 0.5%的阿普拉卡定可确认霍纳综合征,视神经炎性免疫球蛋白G抗体滴度呈阳性。颈椎的磁共振成像显示在左侧更明显的是纵向广泛的髓内扩张病变,造影剂增强后从C2扩展到C5,与视神经炎相同。该患者被诊断为伴有左霍纳综合征的视神经炎。

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