Di Bella P, Logullo F, Dionisi L, Danni M, Scarpelli M, Angeleri F
Istituto delle Molattie del Sistema Nervoso, Università di Ancona.
Ital J Neurol Sci. 1991 Feb;12(1):113-8. doi: 10.1007/BF02337624.
We describe a patient with a chronic acquired predominantly motor polyneuropathy. His clinical picture initially led to a diagnosis of lower motor neuron form of amyotrophic lateral sclerosis. However electrophysiological examination revealed multifocal, prevalently proximal, conduction blocks at sites not prone to compression. Distinguishing this unusual polyneuropathy from motor neuron diseases is critical, since the former is a potentially, treatable disorder.
我们描述了一名患有慢性获得性以运动为主的多神经病患者。他的临床表现最初导致诊断为肌萎缩侧索硬化症的下运动神经元型。然而,电生理检查显示在不易受压部位存在多灶性、主要为近端的传导阻滞。将这种不寻常的多神经病与运动神经元疾病区分开来至关重要,因为前者是一种潜在可治疗的疾病。