Seok Hung Youl
Department of Neurology, School of Medicine, Kyungpook National University, Kyungpook National University Hospital, 130 Dongdeok-ro, Jung-gu, Daegu, 41944, Republic of Korea.
Neurol Sci. 2025 Apr 23. doi: 10.1007/s10072-025-08194-8.
Myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease (MOGAD) is a recently recognized disorder distinct from multiple sclerosis (MS) and neuromyelitis optica spectrum disorder. The introduction of diagnostic criteria for MOGAD in 2023 marked a significant advance, providing high diagnostic accuracy for typical cases. However, challenges arise when patients test positive for MOG antibodies while also meeting the 2017 McDonald criteria for MS. These cases present a diagnostic dilemma, as they blur the lines between MS and MOGAD, complicating treatment decisions. This review addresses the diagnostic and management challenges faced by these patients, highlighting recent studies that underscore the difficulty in distinguishing between these two diseases and offering insights into how to approach these ambiguous cases.
髓鞘少突胶质细胞糖蛋白(MOG)抗体相关疾病(MOGAD)是一种最近才被认识到的疾病,有别于多发性硬化症(MS)和视神经脊髓炎谱系障碍。2023年MOGAD诊断标准的出台是一项重大进展,为典型病例提供了很高的诊断准确性。然而,当患者MOG抗体检测呈阳性,同时又符合2017年MS的麦克唐纳标准时,就会出现挑战。这些病例带来了诊断困境,因为它们模糊了MS和MOGAD之间的界限,使治疗决策变得复杂。这篇综述探讨了这些患者面临的诊断和管理挑战,强调了最近的研究,这些研究突出了区分这两种疾病的困难,并就如何处理这些不明确的病例提供了见解。