Hader W J, Rpzdilsky B, Nair C P
Can J Neurol Sci. 1986 Feb;13(1):66-9. doi: 10.1017/s0317167100035824.
We report the clinical and pathological findings of the unusual combination of two idiopathic central nervous system diseases, multiple sclerosis and amyotrophic lateral sclerosis in a 56 year old physician with a twenty-seven year history of a disease initially characterized by relapses and remissions, followed by an eight year quiescent period. During the last year of life there was rapid deterioration with development of generalized weakness, atrophy, weight loss and fasciculations of body and tongue, and associated difficulty with swallowing and sudden respiratory failure. The autopsy confirmed characteristic "burned out" plaques of multiple sclerosis and anterior horn cell and axonal degeneration of amyotrophic lateral sclerosis.
我们报告了一名56岁医生身上两种特发性中枢神经系统疾病——多发性硬化症和肌萎缩侧索硬化症不寻常组合的临床和病理发现。该患者有27年病史,最初表现为病情复发和缓解,随后有8年的静止期。在生命的最后一年,病情迅速恶化,出现全身无力、萎缩、体重减轻以及身体和舌头的肌束震颤,并伴有吞咽困难和突发呼吸衰竭。尸检证实有多发性硬化症典型的“陈旧性”斑块以及肌萎缩侧索硬化症的前角细胞和轴突变性。