Awerbuch G I, Nigro M A, Sandyk R, Levin J R
Department of Neurology, Children's Hospital of Michigan, Detroit.
Eur Neurol. 1991;31(6):348-51. doi: 10.1159/000116691.
Primary lumbosacral plexus neuropathy (LSPN) is a well-defined syndrome characterized by pain, weakness and atrophy in the distribution of the lumbosacral plexus. Previous reports of LSPN have stressed the benign nature of the syndrome. Patients generally have a nearly complete recovery in months to years following the initial event. Two patients presenting with a relapsing form of LSPN are reported. The diagnosis of LSPN was based on clinical and electromyographic features, and no underlying cause was found on initial evaluation or subsequent follow-up over a 6- to 8-year period. We suggest that these patients represent a clinically and possibly pathologically distinct subgroup of LSPN.
原发性腰骶丛神经病(LSPN)是一种明确的综合征,其特征为腰骶丛分布区域出现疼痛、无力和萎缩。先前关于LSPN的报告强调了该综合征的良性性质。患者通常在初始事件后的数月至数年中几乎完全康复。本文报告了两名表现为复发性LSPN的患者。LSPN的诊断基于临床和肌电图特征,在初始评估或随后6至8年的随访中未发现潜在病因。我们认为这些患者代表了LSPN在临床和可能在病理上不同的亚组。