Department of Neuroradiology, Pitié Salpêtrière Hospital, APHP, 47-83, boulevard de l'Hôpital, 75013 Paris, France.
Department of Neurology, Hôpital Fondation Adolphe de Rothschild Paris Paris, France.
Rev Neurol (Paris). 2021 Jan-Feb;177(1-2):39-50. doi: 10.1016/j.neurol.2020.06.016. Epub 2020 Oct 10.
Our knowledge of the radiological spectrum of myelin oligodendrocyte glycoprotein antibody associated disease (MOGAD) is growing rapidly. An update on the radiological features of the disease, and its evolution is thus necessary. Magnetic resonance imaging (MRI) has an increasingly important role in the differential diagnosis of MOGAD particularly from aquaporin-4 antibody-positive neuromyelitis optica spectrum disorder (AQP4-NMOSD), and multiple sclerosis (MS). Differentiating these conditions is of prime importance because the management is different between the three inflammatory diseases, and thus could prevent further attack-related disability. Therefore, identifying the MRI features suggestive of MOGAD has diagnostic and prognostic implications. We herein review optic nerve, spinal cord and the brain MRI findings from MOGAD adult patients, and compare them to AQP4-NMOSD and MS.
我们对髓鞘少突胶质细胞糖蛋白抗体相关疾病(MOGAD)的放射学谱的了解正在迅速增加。因此,有必要更新该疾病的放射学特征及其演变。磁共振成像(MRI)在 MOGAD 的鉴别诊断中,特别是在水通道蛋白-4 抗体阳性视神经脊髓炎谱系障碍(AQP4-NMOSD)和多发性硬化(MS)中,具有越来越重要的作用。区分这些疾病非常重要,因为这三种炎症性疾病的治疗方法不同,因此可以防止进一步的攻击相关残疾。因此,识别提示 MOGAD 的 MRI 特征具有诊断和预后意义。本文综述了 MOGAD 成年患者的视神经、脊髓和脑部 MRI 表现,并将其与 AQP4-NMOSD 和 MS 进行了比较。