Garcés Sánchez M, Villanueva-Haba V E, Sevilla Mantecón T, Mayordomo Fernández F, Vílchez Padilla J J
Servicio de Neurología, Hospital Universitario La Fe, Valencia, España.
Neurologia. 2002 Dec;17(10):616-20.
Nonsystemic vasculitic neuropathy (NSVN) is an infrequent type of vasculitic neuropathy that evolves without manifestations of vasculitis in other organs and in the absence of serological abnormalities. There are non clarified conjectures about the pathogenesis, outcome and treatment approach.
A retrospective study of a series of six patients diagnosed of NSVN during a period of 12 years. Clinical, electrophysiological and pathological features, as well as the response to therapy and outcome are analysed.
Four cases presented with a pattern of multiple mononeuropathy, evolving towards a symmetrical sensory and motor polyneuropathy in two of them. One patient presented with an acute sensory neuropathy and another had a subacute asymmetric sensory and motor neuropathy. No signs of accompanying systemic vasculitis were observed during the follow-up (mean 35 months) and the only outstanding serological abnormality was the presence of antibodies against hepatitis B virus in four of them. The nerve conduction studies showed typical features of axonal degeneration. The diagnostic was obtained due to the presence of a necrotizing vasculitis in the sural nerve biopsy in all cases. The mean time from symptom onset to diagnosis was 11 months. All patients were treated with immunosuppressive therapy presenting a favourable response, except the case of the sensory neuropathy that remained stable.
NSVN is a benign type of vasculitic neuropathy with a variable clinical pattern of presentation and favourable response to immunosuppression. This neuropathy requires a high index of suspicion for diagnosis, so nerve biopsy must be carried out in all neuropathy of unknown etiology. Careful follow-up of patients is necessary, so that life-threatening systemic vasculitis neuropathy can be diagnosed early.
非系统性血管炎性神经病(NSVN)是一种罕见的血管炎性神经病类型,其病情发展时其他器官无血管炎表现且无血清学异常。关于其发病机制、预后及治疗方法尚无明确的推测。
对12年间确诊的6例NSVN患者进行回顾性研究。分析其临床、电生理和病理特征,以及治疗反应和预后。
4例表现为多灶性单神经病模式,其中2例逐渐发展为对称性感觉和运动性多发性神经病。1例患者表现为急性感觉神经病,另1例有亚急性不对称性感觉和运动神经病。随访期间(平均35个月)未观察到伴随系统性血管炎的迹象,唯一显著的血清学异常是4例患者存在抗乙型肝炎病毒抗体。神经传导研究显示轴索性变性的典型特征。所有病例均因腓肠神经活检发现坏死性血管炎而确诊。从症状出现到诊断的平均时间为11个月。除感觉神经病患者病情稳定外,所有患者均接受免疫抑制治疗且反应良好。
NSVN是一种良性血管炎性神经病,临床表现多样,对免疫抑制治疗反应良好。这种神经病诊断时需要高度怀疑,因此对于所有病因不明的神经病都必须进行神经活检。对患者进行仔细随访很有必要,以便能早期诊断出危及生命的系统性血管炎性神经病。