Panegyres P K, Blumbergs P C, Leong A S, Bourne A J
Department of Neurology, Queen Elizabeth Hospital, Adelaide, SA.
J Neurol Sci. 1990 Dec;100(1-2):193-202. doi: 10.1016/0022-510x(90)90033-j.
In order to elucidate the pathogenesis of vasculitis in muscle and nerve a clinicopathological study was performed in 23 patients. The patients could be classified into three groups: I multisystem vasculitis (n = 4); II multisystem disease with vasculitis detectable in nerve, muscle, or both (n = 11); and III localised disease with vasculitis in nerve, muscle, or both (n = 8). Ten of 23 patients had vasculitis in both muscle and nerve biopsies; 6 from groups I and II, and 4 from group III indicating that vasculitis confined to muscle and nerve represents a distinct clinicopathological entity. The neuromuscular manifestations in the 23 patients were sensori-motor polyneuropathy (n = 9), mononeuritis multiplex (n = 6), mononeuropathy (n = 3), proximal myopathy (n = 4), and muscle tenderness without weakness (n = 1). Sensori-motor polyneuropathy was found in 8/11 patients from group II, and mononeuritis multiplex in 5/8 patients from group III. Immunotypic analysis, and immunofluorescence patterns indicate that the pathogenesis of vasculitis in muscle and nerve is heterogeneous and suggest that cell mediated and immune complex mechanisms predominate and may be operative in all three patient groups, with an antibody-mediated humoral mechanism in some patients with paraproteinaemic states (group II).
为了阐明肌肉和神经血管炎的发病机制,对23例患者进行了临床病理研究。患者可分为三组:I组为多系统血管炎(n = 4);II组为多系统疾病,在神经、肌肉或两者中可检测到血管炎(n = 11);III组为局限于神经、肌肉或两者的局部疾病(n = 8)。23例患者中有10例在肌肉和神经活检中均发现血管炎;I组和II组各6例,III组4例,这表明局限于肌肉和神经的血管炎代表一种独特的临床病理实体。23例患者的神经肌肉表现为感觉运动性多发性神经病(n = 9)、多灶性单神经病(n = 6)、单神经病(n = 3)、近端肌病(n = 4)和无肌无力的肌肉压痛(n = 1)。II组11例患者中有8例出现感觉运动性多发性神经病,III组8例患者中有5例出现多灶性单神经病。免疫类型分析和免疫荧光模式表明,肌肉和神经血管炎的发病机制是异质性的,提示细胞介导和免疫复合物机制占主导地位,可能在所有三组患者中都起作用,在一些副蛋白血症状态的患者(II组)中存在抗体介导的体液机制。