Barohn R J, Saperstein D S
Department of Neurology, University of Texas Southwestern Medical Center, Dallas 75235-8897, USA.
Semin Neurol. 1998;18(1):49-61. doi: 10.1055/s-2008-1040861.
Acute and chronic inflammatory demyelinating polyneuropathies represent an important group of disorders. Although the acute form is more common, all clinical neurologists will eventually encounter patients with these disorders. Acute inflammatory demyelinating polyneuropathy, or Guillain-Barré syndrome, is the most common cause of acute generalized weakness. Chronic inflammatory demyelinating polyneuropathy, characterized by progressive or relapsing weakness, is important to recognize because it represents a significant number of all initially undiagnosed acquired neuropathies. There are a variety of reasonable therapies available for both of these acquired demyelinating neuropathies. Recently much has been learned about pathogenesis and treatment. This review describes the clinical presentations, laboratory studies, diagnostic criteria, treatment, and prognosis for each disorder.
急性和慢性炎性脱髓鞘性多发性神经病是一组重要的疾病。虽然急性形式更为常见,但所有临床神经科医生最终都会遇到患有这些疾病的患者。急性炎性脱髓鞘性多发性神经病,即吉兰-巴雷综合征,是急性全身性无力的最常见原因。慢性炎性脱髓鞘性多发性神经病以进行性或复发性无力为特征,认识到这一点很重要,因为它在所有最初未确诊的获得性神经病中占相当比例。对于这两种获得性脱髓鞘性神经病,有多种合理的治疗方法。最近,人们对发病机制和治疗有了很多了解。这篇综述描述了每种疾病的临床表现、实验室检查、诊断标准、治疗和预后。