Tsz Wai Yeung, Vincent Lai , Hin Yue Lau , Yiu Chung Wong
{"title":"Moyamoya syndrome associated with systemic lupus erythematosus: A case report and literature review","authors":"Tsz Wai Yeung, Vincent Lai , Hin Yue Lau , Yiu Chung Wong","doi":"10.1016/j.ejrex.2011.04.008","DOIUrl":null,"url":null,"abstract":"<div><p>Moyamoya disease<span><span> is a chronic occlusive cerebrovascular disease affecting young patients. Its association with </span>systemic lupus erythematosus (SLE) has not been well established though had been reported. Their similar acute neurological presentations can lead to diagnostic dilemma. We present a young Chinese female with known SLE initially presenting with unilateral moyamoya phenomenon, subsequently progressed to typical bilateral moyamoya disease 5 years later. We also compare various clinical parameters with other reported cases in past literatures.</span></p></div>","PeriodicalId":100506,"journal":{"name":"European Journal of Radiology Extra","volume":"79 1","pages":"Pages e23-e26"},"PeriodicalIF":0.0000,"publicationDate":"2011-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.ejrex.2011.04.008","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Radiology Extra","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1571467511000575","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
Moyamoya disease is a chronic occlusive cerebrovascular disease affecting young patients. Its association with systemic lupus erythematosus (SLE) has not been well established though had been reported. Their similar acute neurological presentations can lead to diagnostic dilemma. We present a young Chinese female with known SLE initially presenting with unilateral moyamoya phenomenon, subsequently progressed to typical bilateral moyamoya disease 5 years later. We also compare various clinical parameters with other reported cases in past literatures.