Wee A S
Electromyography Laboratory, Department of Neurology, University of Mississippi Medical Center, Jackson, Mississippi 39216, USA.
Electromyogr Clin Neurophysiol. 2004 Oct-Nov;44(7):443-6.
A 32-year-old man with myotonia congenita (Becker type) sustained multiple gunshot wounds. These produced a partial thoracic spinal cord injury and a severe sciatic nerve injury. Six days following the incident, clinical (percussion) and electrophysiologic (EMG) myotonia could be elicited in paretic leg muscles resulting both from the myelopathy and peripheral nerve disruption. Eight months later, the myotonia was no longer present in denervated muscles from the sciatic nerve injury, but was still noted in muscles with upper-motor neuron weakness from the myelopathy. Although myotonia is related principally to abnormalities in the muscle fiber itself, it appears that it is also dependent upon the structural integrity of the peripheral nerve supply to the muscle for myotonia to continue to occur. The findings in this patient suggest that myotonia may well have diminished and disappeared in muscles shortly after the nerves had undergone Wallerian degeneration. Myotonia does not recur if there is no significant reinnervation.
一名32岁的先天性肌强直(贝克尔型)男性遭受多处枪伤。这些枪伤导致了部分胸段脊髓损伤和严重的坐骨神经损伤。事件发生六天后,在因脊髓病和周围神经损伤而出现麻痹的腿部肌肉中,可诱发临床(叩诊)和电生理(肌电图)肌强直。八个月后,坐骨神经损伤导致的失神经肌肉中不再存在肌强直,但脊髓病导致的上运动神经元无力的肌肉中仍可观察到肌强直。虽然肌强直主要与肌纤维本身的异常有关,但似乎它也依赖于肌肉周围神经供应的结构完整性,以便肌强直持续发生。该患者的研究结果表明,在神经发生华勒变性后不久,肌肉中的肌强直很可能已经减轻并消失。如果没有明显的神经再支配,肌强直不会复发。