Department of Neurology, Chungbuk National University College of Medicine, Cheongju, Chungbuk, Republic of Korea.
J Clin Neurosci. 2011 Sep;18(9):1274-5. doi: 10.1016/j.jocn.2011.01.010. Epub 2011 Jul 8.
Myasthenia gravis (MG) with muscle-specific tyrosine kinase (MuSK) antibody (MuSK-MG) is often associated with prominent facial and bulbar muscle atrophy. It remains unclear whether the muscle atrophy is a consequence of long-term corticosteroid treatment, or of the disease process per se. Herein, we report a steroid-naive patient with MuSK-MG who presented with severe weakness and marked atrophy of the facial and tongue muscles.
重症肌无力(MG)伴肌肉特异性酪氨酸激酶(MuSK)抗体(MuSK-MG)常伴有明显的面肌和球部肌肉萎缩。目前尚不清楚肌肉萎缩是长期皮质类固醇治疗的结果,还是疾病本身的结果。本文报告了一例初发的 MuSK-MG 患者,表现为严重的肌无力和明显的面肌和舌肌无力。