Achari A N, Trontelj J V, Campos D J
Neurology. 1976 Jun;26(6 PT 1):544-6. doi: 10.1212/wnl.26.6.544.
A 34-year-old woman with long-standing multiple sclerosis had a 2-year history and physical signs of myasthenia gravis. The edrophonium chloride (Tensilon) test was positive. Repetitive stimulation of the ulnar nerve at 3 Hz did not show evidence of myasthenic response; however, a single-fiber electromyography demonstrated evidence of neuromuscular block as seen in myasthenia gravis, which was reversed to normal after intravenously administered edrophonium. The patient improved on anticholinesterase medication. It is suggested that patients with multiple sclerosis who have unusual features such as in the patient reported here should be investigated for the presence of myasthenia gravis to ensure proper treatment.
一名患有长期多发性硬化症的34岁女性有重症肌无力的2年病史及体征。依酚氯铵(腾喜龙)试验呈阳性。以3赫兹频率重复刺激尺神经未显示重症肌无力反应的证据;然而,单纤维肌电图显示出如重症肌无力中所见的神经肌肉阻滞证据,静脉注射依酚氯铵后该证据恢复正常。该患者使用抗胆碱酯酶药物后病情改善。建议对有多发性硬化症且具有如本文所报告患者那样不寻常特征的患者进行重症肌无力检查,以确保得到恰当治疗。