Jawdat Omar, Statland Jeffrey M, Barohn Richard J, Katz Jonathan S, Dimachkie Mazen M
Department of Neurology, University of Kansas Medical Center, 3901 Rainbow Boulevard, Mailstop 2012, Kansas City, KS 66160, USA.
Department of Neurology, University of Kansas Medical Center, 3901 Rainbow Boulevard, Mailstop 2012, Kansas City, KS 66160, USA.
Neurol Clin. 2015 Nov;33(4):775-85. doi: 10.1016/j.ncl.2015.07.003. Epub 2015 Sep 8.
Amyotrophic lateral sclerosis (ALS), a rapidly progressive, invariably fatal disease, involves mixed upper and lower motor neurons in different spinal cord regions. Patients with bulbar onset progress more rapidly than patients with limb onset or with a lower motor neuron presentation. Recent descriptions of regional variants suggest some patients have ALS isolated to a single spinal region for many years, including brachial amyotrophic diplegia, leg amyotrophic diplegia, and isolated bulbar palsy. Clearer definitions of regional variants will have implications for prognosis, understanding the pathophysiology of ALS, identifying genetic factors related to slower disease progression, and future planning of clinical trials.
肌萎缩侧索硬化症(ALS)是一种快速进展、不可避免会致命的疾病,累及不同脊髓区域的上下运动神经元。延髓起病的患者比肢体起病或下运动神经元表现的患者进展更快。近期对区域变异型的描述表明,一些患者多年来ALS局限于单一脊髓区域,包括臂丛性肌萎缩性双侧瘫、腿部肌萎缩性双侧瘫和孤立性延髓麻痹。对区域变异型更清晰的定义将对预后、理解ALS的病理生理学、识别与疾病进展较慢相关的遗传因素以及未来临床试验的规划产生影响。