Walton Centre NHS Foundation Trust, Liverpool, UK
Walton Centre NHS Foundation Trust, Liverpool, UK.
Clin Med (Lond). 2019 Mar;19(2):169-176. doi: 10.7861/clinmedicine.19-2-169.
Neuromyelitis optica spectrum disorder (NMOSD) is an uncommon antibody-mediated disease of the central nervous system. Long segments of spinal cord inflammation (myelitis), severe optic neuritis, and/or bouts of intractable vomiting and hiccoughs (area postrema syndrome) are classic presentations of the disease and may alert the clinician to the diagnosis. Untreated, approximately 50% of NMOSD patients will be wheelchair users and blind, and a third will have died within 5 years of their first attack. Unlike multiple sclerosis, a progressive clinical course is very unusual and the accrual of disability is related to relapses. Approximately 75% of patients have antibodies against aquaporin-4, a water channel expressed on astrocytes. Relapses are treated aggressively to prevent residual disability with high-dose steroids and often plasma exchange. Relapse prevention is crucial and achieved with long-term immunosuppression. In this article we review the pathogenesis, clinical features, diagnosis and management of NMOSD.
视神经脊髓炎谱系疾病(NMOSD)是一种罕见的中枢神经系统抗体介导疾病。长节段脊髓炎症(脊髓炎)、严重视神经炎和/或顽固性呕吐和呃逆(极后区综合征)发作是该病的典型表现,并可能提示临床医生进行诊断。未经治疗,约 50%的 NMOSD 患者将成为轮椅使用者和失明者,三分之一的患者在首次发作后 5 年内死亡。与多发性硬化症不同,进行性临床病程非常罕见,残疾的累积与复发有关。约 75%的患者存在针对水通道蛋白-4(星形胶质细胞上表达的水通道)的抗体。复发时使用大剂量类固醇和经常进行血浆置换积极治疗以预防残留残疾。预防复发至关重要,通过长期免疫抑制来实现。本文综述了 NMOSD 的发病机制、临床特征、诊断和治疗。