抗髓鞘少突胶质细胞糖蛋白抗体表现为儿童患者的膨生性脱髓鞘和偏瘫

M. N, Architha G, Jyotsna A, S Prashanth, Ramu A, M R Savitha
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引用次数: 0

摘要

抗髓鞘少突胶质细胞糖蛋白(MOG)抗体相关疾病是一种免疫介导的中枢神经系统脱髓鞘疾病,具有多种表型表现,如急性播散性脑脊髓炎、视神经炎和横切性脊髓炎,但很少表现为扩散性病变,特别是在儿童中。我们提出一个案例的青春期女孩与抗MOG抗体相关的疾病,表现为肿瘤病变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-myelin oligodendrocyte glycoprotein – antibody presenting as tumefactive demyelination and hemiparesis in a pediatric patient
Anti-myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease is an immune-mediated central nervous system demyelinating disorder with a variety of phenotypic presentations such as acute disseminated encephalomyelitis, optic neuritis, and transverse myelitis but rarely presents as tumefactive lesion, particularly in children. We present a case of an adolescent girl with an anti MOG antibody-related disorder that manifested as a tumefactive lesion.
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