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首页> 外文期刊>Neuromuscular disorders: NMD >Prepubertal anti-Musk positive myasthenia gravis with long remission
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Prepubertal anti-Musk positive myasthenia gravis with long remission

机译:青春期前抗麝香阳性重症肌无力,长期缓解

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摘要

Anti-MuSK positive myasthenia gravis (MuSK-MG) is rare prepuberty. We report a female patient with MuSK-MG starting at 3.5. years with ptosis as the sole symptom for 2. years. A brief period of generalization was followed by complete stable remission for 6. years. Prolonged ocular symptoms and long remissions are not features of MuSK-MG, but are often seen in prepubertal onset MG. The patient then presented at age 12 with moderately severe symptoms which were almost confined to oculobulbar muscles and were unresponsive to pyridostigmine. She was dependent on corticosteroids and thymectomy did not seem to be effective. She was later noted to have tongue atrophy after a period without treatment. Our patient thus presented with features seen in many prepubertal patients, but the later course was quite typical of MuSK-MG.
机译:抗MuSK阳性重症肌无力(MuSK-MG)是罕见的青春期前。我们报告了一位女性患者,MuSK-MG的发病率始于3.5岁。上睑下垂为唯一症状两年。短暂的泛化之后是6年的完全稳定缓解。长期的眼部症状和长时间的缓解不是MuSK-MG的特征,但经常在青春期前的MG中看到。然后,患者在12岁时出现中度严重症状,几乎局限于眼球肌,对吡啶斯的明无反应。她依赖皮质类固醇,胸腺切除术似乎无效。后来发现她未经治疗一段时间后出现舌头萎缩。因此,我们的患者表现出许多青春期前患者所见的特征,但后来的病程是MuSK-MG的典型症状。

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