首页> 美国卫生研究院文献>BMJ Case Reports >Leber’s hereditary optic neuropathy misdiagnosed as optic neuritis and Lyme disease in a patient with multiple sclerosis
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Leber’s hereditary optic neuropathy misdiagnosed as optic neuritis and Lyme disease in a patient with multiple sclerosis

机译:Leber的遗传视神经病变被误诊为具有多发性硬化症的患者的视神经炎和莱姆病

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摘要

A 28-year-old Caucasian man developed sudden painless vision loss in the right eye. He was diagnosed with optic neuritis. MRI showed white matter lesions consistent with multiple sclerosis (MS), but no optic nerve enhancement. Eight months later, the left eye was affected in the same manner. Examination showed right optic atrophy and apparent left optic disc swelling. Workup revealed positive Lyme IgG. Differential diagnosis included optic neuritis and Lyme optic neuropathy, and he was treated with intravenous steroids, intravenous immunoglobulin, plasmapheresis and intravenous ceftriaxone without improvement. Neuro-ophthalmology consultation led to identification of pseudo-optic disc oedema, and Leber’s hereditary optic neuropathy (LHON) was suspected and confirmed by genetic testing. LHON may occur in association with MS, and should be considered in patients with MS with vision loss atypical for optic neuritis. This is especially important as new treatments for LHON (including gene therapy) are currently undergoing clinical trials.
机译:一个28岁的白人男子在右眼开发了突然的无痛视力丧失。他被诊断出患有视神经炎。 MRI显示白质病变与多发性硬化(MS)一致,但没有视神经增强。八个月后,左眼以同样的影响。检查显示右光学萎缩和明显的左视碟肿胀。次数显示出阳性莱姆IgG。鉴别诊断包括视神经炎和莱姆视神经病变,他被静脉内固醇,静脉内免疫球蛋白,血浆丸剂和静脉注射头孢菌治疗而没有改善。神经眼科咨询导致伪光盘水肿的识别,并通过遗传检测进行怀疑和证实Leber的遗传视神经病变(LHON)。 Lhon可能与MS相关联,并且应该在MS患者中考虑具有视觉丧失非典型的视神经炎。这尤其重要,因为目前正在进行临床试验的LHON(包括基因治疗)的新治疗。

著录项

  • 期刊名称 BMJ Case Reports
  • 作者

    Melinda Chang;

  • 作者单位
  • 年(卷),期 2018(11),1
  • 年度 2018
  • 页码 e227109
  • 总页数 3
  • 原文格式 PDF
  • 正文语种
  • 中图分类
  • 关键词

    机译:神经眼科;多发性硬化;视觉途径;

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