{"title":"埃文综合症-一个病例报告","authors":"B. N","doi":"10.23880/hij-16000174","DOIUrl":null,"url":null,"abstract":"Evan’s syndrome is a rare and chronic autoimmune disease characterised by autoimmune hemolytic anemia and immune thrombocytopenic purpura with a positive Coomb’s test in the absence of an underlying etiology. Majority of the patients with this syndrome have a chronic relapsing course and significant morbidity and mortality despite treatment. We present a case of a 22 year old female, in which, based on the clinical features, Coombs test, hemolytic anemia and thrombocytopenia, a diagnosis of Evans syndrome was made.","PeriodicalId":245976,"journal":{"name":"Haematology International Journal","volume":"38 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Evan’s Syndrome - A Case Report\",\"authors\":\"B. N\",\"doi\":\"10.23880/hij-16000174\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Evan’s syndrome is a rare and chronic autoimmune disease characterised by autoimmune hemolytic anemia and immune thrombocytopenic purpura with a positive Coomb’s test in the absence of an underlying etiology. Majority of the patients with this syndrome have a chronic relapsing course and significant morbidity and mortality despite treatment. We present a case of a 22 year old female, in which, based on the clinical features, Coombs test, hemolytic anemia and thrombocytopenia, a diagnosis of Evans syndrome was made.\",\"PeriodicalId\":245976,\"journal\":{\"name\":\"Haematology International Journal\",\"volume\":\"38 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1900-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Haematology International Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.23880/hij-16000174\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Haematology International Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.23880/hij-16000174","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Evan’s syndrome is a rare and chronic autoimmune disease characterised by autoimmune hemolytic anemia and immune thrombocytopenic purpura with a positive Coomb’s test in the absence of an underlying etiology. Majority of the patients with this syndrome have a chronic relapsing course and significant morbidity and mortality despite treatment. We present a case of a 22 year old female, in which, based on the clinical features, Coombs test, hemolytic anemia and thrombocytopenia, a diagnosis of Evans syndrome was made.