Mistakes in the diagnosis of neuromyelitis optic spectrum diseases lead to wrong therapy and deterioration of patients’ condition

铅(地质) 医学 视神经脊髓炎 光谱紊乱 重症监护医学 皮肤病科 多发性硬化 免疫学 精神科 生物 古生物学
作者
O. V. Boyko,M. A. Omarova,V V Gosteva,А. А. Кузнецов,Alexey Boykо
出处
期刊:Zhurnal Nevrologii I Psikhiatrii Imeni S S Korsakova [Media Sphere Publishing Group]
卷期号:124 (7): 96-96
标识
DOI:10.17116/jnevro202412407296
摘要

Neuromyelitis optic spectrum diseases (NMOSD) are a group of rare neuroimmunological diseases involving mainly the optic nerves and spinal cord, to a lesser extent the brain, and causing severe exacerbations that lead to persistent disability of patients. For many years, opticoneuromyelitis was considered a prognostically unfavorable variant of the course of multiple sclerosis (MS), however, in 2004, specific autoantibodies to aquaporin-4 were found in such patients, which made it possible to isolate NMOSD into a separate group of demyelinating diseases other than MS. Due to similar clinical signs and the predominantly remitting course of diseases, it is often difficult to make a correct diagnosis and, accordingly, prescribe effective therapy, which often leads to incorrectly selected therapy with incorrect diagnosis. In some cases, this leads to a worsening of the course of NMOSD. We present a case of late diagnosis of NMOSD that confirms the development of exacerbation in the patient 2 months after the first course of therapy with alemtuzumab prescribed as a highly effective therapy for highly active remitting MS. Timely diagnosis of NMOSD makes it possible to exclude such cases.

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