Beck Goichi, Yabumoto Taiki, Baba Kousuke, Sasaki Tsutomu, Higuchi Osamu, Matsuo Hidenori, Mochizuki Hideki
Department of Neurology, Osaka University Graduate School of Medicine, Japan.
Intern Med. 2016;55(22):3361-3363. doi: 10.2169/internalmedicine.55.7030. Epub 2016 Nov 15.
We herein report the case of a 72-year-old man demonstrating myasthenia gravis (MG) with a dropped head and acute respiratory insufficiency. There was no ocular, bulbar, or limb involvement. The patient was seronegative for anti-acetylcholine receptor (AChR) antibodies and anti-muscle-specific tyrosine kinase (MuSK) antibodies. Subsequent tests showed seropositivity for anti-low-density lipoprotein receptor-related protein 4 (LRP4) antibodies. The addition of steroid pulse therapy resulted in a full remission of his respiratory symptoms. This presentation suggests that LRP4-positive MG should be considered in the differential diagnosis of patients presenting with acute respiratory insufficiency without either cranial or limb involvement.
我们在此报告一例72岁男性,表现为重症肌无力(MG)伴头部下垂和急性呼吸功能不全。无眼部、延髓或肢体受累。该患者抗乙酰胆碱受体(AChR)抗体和抗肌肉特异性酪氨酸激酶(MuSK)抗体血清学检查均为阴性。随后的检查显示抗低密度脂蛋白受体相关蛋白4(LRP4)抗体血清学阳性。加用类固醇脉冲疗法后,其呼吸症状完全缓解。该病例提示,在鉴别诊断无头颅或肢体受累的急性呼吸功能不全患者时,应考虑LRP4阳性的MG。