Department of Neurology, Graduate School of Medicine, Chiba University, Japan.
Department of Neurology, National Hospital Organization Chibahigashi National Hospital, Japan.
Intern Med. 2021 Aug 15;60(16):2671-2675. doi: 10.2169/internalmedicine.6834-20. Epub 2021 Mar 1.
We herein report a case of seronegative immune-mediated necrotizing myopathy (IMNM) concurrent with anti-Kv1.4 and anti-titin antibodies. A 72-year-old Japanese woman presented with a 29-year history of fluctuating high serum creatine kinase (CK) levels followed by intermittent ptosis and respiratory muscle weakness. This case highlights the fact that marked respiratory muscle weakness requiring intubation can be seen in an ambulant patient with IMNM. Marked respiratory muscle weakness, rhabdomyolysis-like acute elevation of CK levels, and anti-striational muscle antibodies may be a characteristic constellation of findings in a distinct subgroup of patients with inflammatory myopathy with myasthenia gravis or similar symptoms.
我们在此报告一例血清阴性免疫介导性坏死性肌病(IMNM)合并抗 Kv1.4 和抗肌联蛋白抗体。一名 72 岁日本女性,29 年前出现波动升高的血清肌酸激酶(CK)水平,随后间歇性出现眼睑下垂和呼吸肌无力。本例突出表明,在 IMNM 患者中,即使能走动,也可能出现显著的呼吸肌无力而需要插管。显著的呼吸肌无力、横纹肌溶解样 CK 水平急性升高和抗肌节肌肉抗体可能是一组具有重症肌无力或类似症状的炎症性肌病患者的特征性表现。