Adams D, Kuntzer T, Steck A J, Lobrinus A, Janzer R C, Regli F
Centre Hospitalier, Universitaire Vaudois, Lausanne, Switzerland.
J Neurol Neurosurg Psychiatry. 1993 Sep;56(9):982-7. doi: 10.1136/jnnp.56.9.982.
A patient with a progressive lower motor neuron syndrome and neurophysiological evidence of motor axon loss, multifocal proximal motor nerve conduction block, and high titres of anti-ganglioside GM1 antibodies. Neuropathological findings included a predominantly proximal motor radiculoneuropathy with multifocal IgG and IgM deposits on nerve fibres associated with a loss of spinal motor neurons. These findings support an autoimmune origin of this lower motor neuron syndrome with retrograde degeneration of spinal motor neurons and severe neurogenic muscular atrophy.
一名患有进行性下运动神经元综合征的患者,具有运动轴突丧失、多灶性近端运动神经传导阻滞的神经生理学证据以及高滴度的抗神经节苷脂GM1抗体。神经病理学发现包括主要为近端运动性神经根神经病,神经纤维上有多处IgG和IgM沉积,伴有脊髓运动神经元丧失。这些发现支持这种下运动神经元综合征的自身免疫起源,伴有脊髓运动神经元的逆行性变性和严重的神经源性肌肉萎缩。