首页> 美国卫生研究院文献>Frontiers in Neurology >Myasthenia Gravis With Reversible Pyramidal Tract Damage and Pseudo Internuclear Ophthalmoplegia. A Case Report and Literature Review
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Myasthenia Gravis With Reversible Pyramidal Tract Damage and Pseudo Internuclear Ophthalmoplegia. A Case Report and Literature Review

机译:重症肌无力伴可逆性锥体束损伤和假性核间眼肌麻痹。病例报告及文献复习

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摘要

Myasthenia gravis (MG) is a rare and treatable antibody-mediated autoimmune disease. Pseudo internuclear ophthalmoplegia (-INO) or pyramidal tract damage is rarely observed in MG, and there were no known cases of MG with both pseudo-INO and pyramidal tract damage. Here, we report a case of a 61-year-old female suffering from MG accompanied by pseudo-INO and pyramidal tract damage with a rapid progressive course. Her blood and cerebrospinal fluid (CSF) tests were normal, except for the presence of the anti-acetylcholine receptor antibody. CT and contrast enhancement of the chest showed a thymic involution. MRI and contrast enhancement images of the brain and whole spine were normal. Both the clinical response to the administration of neostigmine and the repetitive nerve stimulation test were positive. The motor evoked potentials at lower limb recordings were normal. According to her signs, symptoms, decrementing response on repetitive stimulation test, elevated anti-acetylcholine receptor antibody and positive response to neostigmine, the patient was diagnosed as having MG. After treatment with pyridostigmine, intravenous immunoglobulin, prednisone acetate tablets and methotrexate, all her symptoms disappeared, including pseudo-INO and pyramidal tract damage. To our best knowledge, this is the first report of a case of MG with both pseudo-INO and pyramidal tract damage. Based on our case and a review of the literature, we propose that pyramidal tract damage and pseudo-INO can be two signs of MG, and that MG can cause damage to other systems besides neuromuscular junctions.
机译:重症肌无力(MG)是一种罕见且可治疗的抗体介导的自身免疫性疾病。在MG中很少观察到假核眼肌麻痹(-INO)或锥体束损伤,也没有已知的MG既有伪INO也有锥体束损伤的病例。在这里,我们报道了一名61岁的女性,患有MG并伴有假性INO和锥体束损伤,并伴有快速进展过程。除了存在抗乙酰胆碱受体抗体外,她的血液和脑脊液(CSF)测试正常。胸部CT和对比增强显示胸腺退化。脑部和整个脊柱的MRI和对比增强图像均正常。新斯的明的给药临床反应和重复性神经刺激试验均呈阳性。下肢记录的运动诱发电位正常。根据她的体征,症状,重复刺激试验的反应减弱,抗乙酰胆碱受体抗体升高以及对新斯的明的阳性反应,该患者被诊断为患有MG。用吡啶斯的明,静脉注射免疫球蛋白,醋酸泼尼松片和甲氨蝶呤治疗后,她的所有症状消失,包括假性INO和锥体束损伤。据我们所知,这是首例同时伴有假INO和锥体束损伤的MG病例。根据我们的案例和文献回顾,我们认为锥体束损伤和伪INO可能是MG的两个征兆,并且MG可能导致除神经肌肉接头外的其他系统损伤。

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