M. N, Architha G, Jyotsna A, S Prashanth, Ramu A, M R Savitha
{"title":"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","authors":"M. N, Architha G, Jyotsna A, S Prashanth, Ramu A, M R Savitha","doi":"10.32677/ijch.v10i3.3871","DOIUrl":null,"url":null,"abstract":"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.","PeriodicalId":22476,"journal":{"name":"The Indian journal of child health","volume":"31 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-03-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Anti-myelin oligodendrocyte glycoprotein – antibody presenting as tumefactive demyelination and hemiparesis in a pediatric patient\",\"authors\":\"M. N, Architha G, Jyotsna A, S Prashanth, Ramu A, M R Savitha\",\"doi\":\"10.32677/ijch.v10i3.3871\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"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.\",\"PeriodicalId\":22476,\"journal\":{\"name\":\"The Indian journal of child health\",\"volume\":\"31 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-03-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Indian journal of child health\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.32677/ijch.v10i3.3871\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Indian journal of child health","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.32677/ijch.v10i3.3871","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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.