Meyrignac C, Poirier J, Degos J D
Eur Neurol. 1985;24(2):115-20. doi: 10.1159/000115771.
A 59-year-old man presented with dyspnoea, hypersomnia followed by acute respiratory failure necessitating mechanical ventilation. There were no signs of cardiopulmonary disease and on the first few days, extubation was impossible. Further neurological evaluation supported the diagnosis of amyotrophic lateral sclerosis. The neuropathological examination corroborated this diagnosis, and showed a preponderance of lesions in the phrenic nuclei and axonal alterations associated with a fast evolution.
一名59岁男性出现呼吸困难、嗜睡,随后发展为急性呼吸衰竭,需要进行机械通气。没有心肺疾病的迹象,在最初几天无法进行拔管。进一步的神经学评估支持肌萎缩侧索硬化症的诊断。神经病理学检查证实了这一诊断,并显示膈神经核病变占优势以及与快速进展相关的轴突改变。