Korczyn A D, Kuritzky A, Sandbank U
J Neurol Sci. 1978 Oct;38(3):399-408. doi: 10.1016/0022-510x(78)90145-4.
A patient with insidious onset of weakness, muscle atrophy and true hypertrophy, and sustained spasms is described. The spasms, initially mistaken to be myotonic, were shown electromyographically to result from sustained activity of the muscle fibres. An additional clinical manifestation verified myographically, was impaired reciprocal inhibition. Also, the patient had thick peripheral nerves and very slow motor (but normal sensory) nerve conduction. Histologic examination of sural nerve biopsy revealed large vacuoles within Schwann cells containing unidentified material, as well as onion-bulb formations. The possibility of a metabolic error resulting in storage of an abnormal material within Schwann cells is assumed.
描述了一名患者,其起病隐匿,有肌无力、肌肉萎缩、真性肥大及持续性痉挛。这些痉挛最初被误诊为肌强直,经肌电图检查显示是由肌纤维的持续性活动引起的。另一个经肌动图证实的临床表现是交互抑制受损。此外,该患者外周神经粗大,运动神经传导速度极慢(但感觉神经传导正常)。腓肠神经活检的组织学检查显示,施万细胞内有大空泡,内含不明物质,以及葱球样结构。推测存在代谢错误导致施万细胞内异常物质蓄积的可能性。