Lagueny A, Coquet M, Julien J, Vital C, Ferrer X, Larrieu J L, Aupy M
Rev Neurol (Paris). 1987;143(3):189-200.
Muscle hypertrophy in neurogenic disorders is an uncommon phenomenon which has been reported in various conditions: hereditary or acquired anterior horn cell diseases, essentially S1 radicular compressions, and polyneuritis generally of a demyelinating type. We report two cases of denervating disease with muscle hypertrophy. The first was an S1 radiculopathy, and the second a compression with ischemia of the spinal cord by herniation of the D11-D12 disc, and showing partial improvement after surgery. In both cases, electrophysiological examination of the hypertrophic muscles revealed abnormal activities identified as complex repetitive discharges. In the second case they were associated with a syndrome of continuous motor unit activity. Such activities are rare in peripheral nerve involvement. However they have quite often been recorded in cases of neurogenic muscle hypertrophy and may therefore be partly responsible for the development of the hypertrophy.
神经源性疾病中的肌肉肥大是一种罕见现象,已在多种情况下被报道:遗传性或获得性前角细胞疾病、主要是S1神经根受压,以及通常为脱髓鞘型的多发性神经炎。我们报告两例伴有肌肉肥大的失神经疾病。第一例是S1神经根病,第二例是D11 - D12椎间盘突出导致脊髓受压并伴有缺血,术后显示部分改善。在这两例中,对肥大肌肉的电生理检查均发现异常活动,被确定为复合重复放电。在第二例中,它们与持续运动单位活动综合征相关。这种活动在周围神经受累中很少见。然而,它们在神经源性肌肉肥大的病例中经常被记录到,因此可能部分导致了肥大的发展。