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慢性复发性(免疫性)多发性神经病:发病机制与治疗

Chronic relapsing (dysimmune) polyneuropathy: pathogenesis and treatment.

作者信息

Dalakas M C, Engel W K

出版信息

Ann Neurol. 1981;9 Suppl:134-45. doi: 10.1002/ana.410090719.

Abstract

Chronic relapsing polyneuropathy is a distinct dysschwannian/demyelinating polyneuropathy characterized by usually slow onset, progressive or relapsing-remitting course, elevated cerebrospinal fluid (CSF) protein, marked slowing of nerve conduction velocity, segmental demyelination demonstrable in sural nerve biopsies, and absence of systemic illness or abnormal serum immunoglobulins. The cause of the disorder and the mechanisms underlying its chronicity and relapsing-remitting course are not clear. Immunoglobulin deposition observed in sural nerve biopsies and abnormal immunoglobulin patterns in the "CSF in some cases suggest a dysimmune pathogenesis; thus the term chronic relapsing (dysimmune) polyneuropathy (CRDP) is preferred. The disease is a treatable form of idiopathic polyneuropathy. In our series of 25 patients with CRDP, treatment with high-single-dose daily prednisone, slowly tapered to an alternate-day program, has been very successful in the majority. A low (10 to 20 mg) alternate-day-single-dose program, maintained indefinitely, seems to be required to prevent future recurrences. Evidence is provided that other immunosuppressants (azathioprine, cyclophosphamide, poly-ICLC) and possibly plasmapheresis, alone or in conjunction with corticosteroids, may have a beneficial role in controlling difficult cases of chronic relapsing polyneuropathy.

摘要

慢性复发性多发性神经病是一种独特的脱髓鞘性多发性神经病,其特征通常为起病缓慢,病程呈进行性或复发-缓解型,脑脊液(CSF)蛋白升高,神经传导速度明显减慢,腓肠神经活检可显示节段性脱髓鞘,且无全身性疾病或血清免疫球蛋白异常。该疾病的病因以及其慢性病程和复发-缓解过程的潜在机制尚不清楚。在腓肠神经活检中观察到免疫球蛋白沉积,以及某些病例中脑脊液的异常免疫球蛋白模式提示存在免疫失调发病机制;因此,慢性复发性(免疫失调性)多发性神经病(CRDP)这一术语更为合适。该疾病是特发性多发性神经病的一种可治疗形式。在我们的25例CRDP患者系列中,采用每日大剂量单剂量泼尼松治疗,然后缓慢减量至隔日方案,大多数患者取得了非常好的疗效。似乎需要无限期维持低剂量(10至20毫克)隔日单剂量方案以预防未来复发。有证据表明,其他免疫抑制剂(硫唑嘌呤、环磷酰胺、聚肌胞苷酸)以及可能的血浆置换,单独或与皮质类固醇联合使用,在控制慢性复发性多发性神经病的难治性病例中可能具有有益作用。

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