Nielsen Helle Hvilsted, Ravnborg Mads, Illes Zsolt
Neurologisk Afdeling, Odense Universitetshospital, Sdr. Boulevard 29, 5000 Odense C.
Ugeskr Laeger. 2014 Jun 23;176(26):V02130104.
Neuromyelitis optica (NMO) is an inflammatory demyelinating disease characterized by antibodies against aquaporin-4 in up to 80% of the cases and even less in the NMO spectrum disorders, which may be difficult to distinguish from early multiple sclerosis. While immunosuppressive therapy should be introduced in definite NMO, treatment strategies of NMO spectrum disorders are less clearly defined. Here, we review the current guidelines for treatment of NMO and NMO spectrum disorders in the light of two cases, and suggest a practical approach to the management of these disorders.
视神经脊髓炎(NMO)是一种炎症性脱髓鞘疾病,高达80%的病例中存在抗水通道蛋白4抗体,在视神经脊髓炎谱系障碍中该比例甚至更低,后者可能难以与早期多发性硬化症相区分。虽然明确诊断的NMO应采用免疫抑制治疗,但视神经脊髓炎谱系障碍的治疗策略尚不明确。在此,我们根据两个病例回顾了目前视神经脊髓炎和视神经脊髓炎谱系障碍的治疗指南,并提出了针对这些疾病管理的实用方法。