Statland Jeffrey M, Barohn Richard J, Dimachkie Mazen M, Floeter Mary Kay, Mitsumoto Hiroshi
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):749-60. doi: 10.1016/j.ncl.2015.07.007. Epub 2015 Sep 8.
Primary lateral sclerosis is characterized by insidious onset of progressive upper motor neuron dysfunction in the absence of clinical signs of lower motor neuron involvement. Patients experience stiffness; decreased balance and coordination; mild weakness; and, if the bulbar region is affected, difficulty speaking and swallowing, and emotional lability. The diagnosis is made based on clinical history, typical examination findings, and diagnostic testing negative for other causes of upper motor neuron dysfunction. Electromyogram is normal, or only shows mild neurogenic findings in a few muscles, not meeting El Escorial criteria. Treatment is largely supportive.
原发性侧索硬化症的特征是隐匿起病,出现进行性上运动神经元功能障碍,而无下运动神经元受累的临床体征。患者会出现僵硬;平衡和协调能力下降;轻度无力;如果延髓区域受累,则会出现说话和吞咽困难以及情绪不稳定。诊断基于临床病史、典型的检查结果以及针对上运动神经元功能障碍的其他病因的诊断测试呈阴性。肌电图正常,或仅在少数肌肉中显示轻度神经源性改变,不符合埃尔埃斯科里亚尔标准。治疗主要是支持性的。