Tenembaum Silvia, Yeh E Ann
Department of Neurology, National Pediatric Hospital Dr. J. Garrahan, Buenos Aires, Argentina.
Division of Neurology, Department of Pediatrics, SickKids Research Institute, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
Front Pediatr. 2020 Jun 25;8:339. doi: 10.3389/fped.2020.00339. eCollection 2020.
Neuromyelitis Optica Spectrum Disorder (NMOSD) is an inflammatory demyelinating disease of the central nervous system (CNS) primarily affecting the optic nerves and spinal cord, but also involving other regions of the CNS including the area postrema, periaqueductal gray matter, and hypothalamus. Knowledge related to pediatric manifestations of NMOSD has grown in recent years, particularly in light of newer information regarding the importance of not only antibodies to aquaporin 4 (AQP4-IgG) but also myelin oligodendrocyte glycoprotein (MOG-IgG) in children manifesting clinically with this syndrome. In this review, we describe the current state of the knowledge related to clinical manifestations, diagnosis, and chronic therapies for children with NMOSD, with emphasis on literature that has been published in the last 5 years. Following the review, we propose recommendations for the assessment/follow up clinical care, and treatment of this population.
视神经脊髓炎谱系障碍(NMOSD)是一种中枢神经系统(CNS)的炎性脱髓鞘疾病,主要影响视神经和脊髓,但也累及CNS的其他区域,包括最后区、导水管周围灰质和下丘脑。近年来,与NMOSD儿童表现相关的知识不断增加,特别是鉴于有了新的信息,即水通道蛋白4抗体(AQP4-IgG)以及髓鞘少突胶质细胞糖蛋白(MOG-IgG)在临床上表现出该综合征的儿童中具有重要意义。在这篇综述中,我们描述了与NMOSD儿童的临床表现、诊断和长期治疗相关的知识现状,重点关注过去5年发表的文献。综述之后,我们针对该人群的评估/随访临床护理和治疗提出建议。