Pollard J D, Selby G
J Neurol Sci. 1978 Jun;37(1-2):113-25. doi: 10.1016/0022-510x(78)90232-0.
A unique case history is presented, of a 42-year-old patient who has suffered three episodes of a demyelinating neuropathy, each of which followed an injection of tetanus toxoid. The clinical features on each occasion were characteristic of acute idiopathic polyneuropathy; a rapid onset of a mainly motor neuropathy with eventual recovery. Nerve conduction studies performed during the second and third episodes demonstrated grossly slowed motor conduction velocities. The sural nerve was biopsied after the third episode, and the features seen on light and electron microscopy included prominent hypertrophic changes, mononuclear cells associated with most "onion bulbs" and macrophage mediated demyelination. Studies of blastogenesis and macrophage migration inhibition, showed T lymphocyte responsiveness to both peripheral nerve myelin and tetanus toxoid. Typing for antigens of the HLA system indicated that the patient was homozygous for HLAB8.
本文报告了一例独特的病例,患者为42岁,曾三次发生脱髓鞘性神经病,每次发作均在注射破伤风类毒素之后。每次发作的临床特征均符合急性特发性多神经病;主要为运动神经病快速起病,最终恢复。在第二次和第三次发作期间进行的神经传导研究显示运动传导速度明显减慢。第三次发作后对腓肠神经进行了活检,光镜和电镜下所见特征包括显著的肥大性改变、与多数“洋葱球”相关的单核细胞以及巨噬细胞介导的脱髓鞘。对淋巴细胞转化和巨噬细胞游走抑制的研究表明,T淋巴细胞对周围神经髓鞘和破伤风类毒素均有反应。对HLA系统抗原进行分型显示,该患者为HLA - B8纯合子。