Gorson Kenneth C
Tufts University School of Medicine, Boston, Massachusetts, USA.
Neurologist. 2007 Jan;13(1):12-9. doi: 10.1097/01.nrl.0000252942.14928.17.
Systemic vasculitis has been classically categorized as a primary disorder, such as polyarteritis nodosa, Churg-Strauss syndrome, and Wegener granulomatous, or as a secondary process, representing a complication from a connective tissue disorder (eg, rheumatoid vasculitis), infection, medication, or malignancy. Peripheral neuropathy is a well-recognized consequence of systemic vasculitis due to peripheral nerve infarction with Wallerian degeneration. Rarely, neuropathy is the sole manifestation of vasculitis, referred to as nonsystemic vasculitic neuropathy (NSVN). These conditions are defined pathologically by tissue biopsy demonstrating disruption or destruction of the vessel wall with inflammatory cell infiltrates.
The diagnosis of vasculitic neuropathy is straightforward in patients with an established diagnosis of systemic vasculitis and classic features of mononeuritis multiplex. Most patients have clinical features of a subacute, progressive, generalized but asymmetric, painful, sensorimotor polyneuropathy. Laboratory tests often indicate features of systemic inflammation, such as an elevated sedimentation rate or positive anti-neutrophil cytoplasmic antibody, and electrodiagnostic evaluation shows multiple mononeuropathies or a confluent, asymmetric axonal neuropathy. Nerve biopsy is necessary to establish the diagnosis in most cases, particularly in patients with NSVN. This review summarizes the current treatment of vasculitic neuropathy.
Long-term immunosuppressive therapy is required in most cases. High-dose prednisone combined with intravenous pulse or oral daily cyclophosphamide is standard initial therapy. In those with NSVN, cyclophosphamide also should be used if prednisone monotherapy is ineffective or the patient relapses with tapering. Other agents, such as azathioprine, methotrexate, intravenous immunoglobulin, mycophenolate mofetil, plasma exchange, and rituximab can be offered to patients who are intolerant or have a contraindication to cyclophosphamide. However, evidence for the benefit of these agents is limited to case reports and small case series.
系统性血管炎传统上被分类为原发性疾病,如结节性多动脉炎、变应性肉芽肿性血管炎和韦格纳肉芽肿,或作为继发性过程,代表结缔组织疾病(如类风湿性血管炎)、感染、药物或恶性肿瘤的并发症。周围神经病变是系统性血管炎的一个公认后果,是由于周围神经梗死伴华勒变性所致。很少见的是,神经病变是血管炎的唯一表现,称为非系统性血管炎性神经病变(NSVN)。这些疾病在病理上通过组织活检来定义,显示血管壁破坏或破坏伴有炎性细胞浸润。
对于已确诊系统性血管炎且有多发性单神经炎典型特征的患者,血管炎性神经病变的诊断很简单。大多数患者具有亚急性、进行性、全身性但不对称、疼痛性感觉运动性多神经病变的临床特征。实验室检查常显示系统性炎症特征,如血沉升高或抗中性粒细胞胞浆抗体阳性,电诊断评估显示多发性单神经病变或融合性、不对称性轴索性神经病变。在大多数情况下,尤其是NSVN患者,需要进行神经活检以确诊。本综述总结了目前血管炎性神经病变的治疗方法。
大多数情况下需要长期免疫抑制治疗。大剂量泼尼松联合静脉脉冲或口服每日环磷酰胺是标准的初始治疗方法。对于NSVN患者,如果泼尼松单药治疗无效或患者在逐渐减量时复发,也应使用环磷酰胺。对于不耐受或有环磷酰胺禁忌证的患者,可以提供其他药物,如硫唑嘌呤、甲氨蝶呤、静脉注射免疫球蛋白、霉酚酸酯、血浆置换和利妥昔单抗。然而,这些药物获益的证据仅限于病例报告和小病例系列。