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MRI 证据显示 MuSK 阳性重症肌无力存在早期肌肉萎缩。

MRI evidence of early muscle atrophy in MuSK positive myasthenia gravis.

机构信息

Neurology Department, University of Athens, Eginition Hospital, Athens, Greece.

出版信息

J Neuroimaging. 2011 Jul;21(3):303-5. doi: 10.1111/j.1552-6569.2009.00456.x. Epub 2009 Dec 4.

Abstract

Muscle atrophy, particularly of facial and bulbar muscles, seems to be a relatively common long-term consequence of musclespecific tyrosine kinase-myasthenia gravis (MuSK-MG), perhaps reflecting the chronic state of disease or long-term therapy with corticosteroids. We performed magnetic resonance imaging (MRI) to assess muscle wasting in the facial and bulbar muscles in two female MuSK-MG patients, with short duration of symptoms prior to diagnosis and prior to commencement of steroid therapy. The study revealed marked atrophy of temporalis, masseters, and lingual muscles with fatty replacement. MRI evidence of early muscle atrophy in MuSK-MG may indicate that MuSK antibodies per se may predispose to muscle atrophy.

摘要

肌肉萎缩,尤其是面肌和球部肌肉萎缩,似乎是肌肉特异性酪氨酸激酶重症肌无力(MuSK-MG)的一种较为常见的长期后果,这可能反映了疾病的慢性状态或长期应用皮质类固醇治疗。我们对两名女性 MuSK-MG 患者进行了磁共振成像(MRI)检查,以评估面部和球部肌肉的肌肉消耗情况,这些患者在诊断前和开始皮质类固醇治疗前的症状持续时间较短。研究显示,颞肌、咬肌和舌肌明显萎缩伴脂肪替代。MuSK-MG 中 MRI 早期肌肉萎缩的证据表明,MuSK 抗体本身可能导致肌肉萎缩。

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