Wilcox P G, Morrison N J, Anzarut A R, Pardy R L
UBC Pulmonary Research Laboratory, St. Paul's Hospital, Vancouver, Canada.
Chest. 1988 Mar;93(3):604-6. doi: 10.1378/chest.93.3.604.
Inspiratory muscle function was assessed in a patient with the Lambert-Eaton myasthenic syndrome that developed in association with a bronchogenic carcinoma. Repetitive maximal inspiratory pressure measurements and the electromyographic response to phrenic nerve stimulation established involvement of the inspiratory muscles in general and the diaphragm specifically in this condition.
对一名患有与支气管源性癌相关的兰伯特-伊顿肌无力综合征的患者进行了吸气肌功能评估。重复进行最大吸气压力测量以及对膈神经刺激的肌电图反应，证实了在这种情况下吸气肌总体受累，尤其是膈肌。
