López-Cabrera Yessica, Aguilar-Silva Andrés, Del Carpio Orantes Luis, Chavez Aguilar Cecilia, Cerda Mendez Carlos Ivan, Onofre Aquino Raquel
{"title":"Case report of Hemophagocytic Syndrome complicated by septic shock","authors":"López-Cabrera Yessica, Aguilar-Silva Andrés, Del Carpio Orantes Luis, Chavez Aguilar Cecilia, Cerda Mendez Carlos Ivan, Onofre Aquino Raquel","doi":"10.15761/CCRR.1000495","DOIUrl":null,"url":null,"abstract":"The incidence varies according to regions, with a predominance in pediatric patients. In adults, there has been an average age of onset at 50 years with a female predominance in a 1:7 with respect to the men [3]. An estimated worldwide incidence of 1.2 cases per million inhabitants. In Latin America, there is no standardized report that allows establishing epidemiological data, with an estimated survival of 38% one year after diagnosis [4] (Figure 1). However, this figure may be underestimated as it is a diagnosis of exclusion and due to the lack of specificity of the clinical picture.","PeriodicalId":72607,"journal":{"name":"Clinical case reports and reviews","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical case reports and reviews","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15761/CCRR.1000495","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The incidence varies according to regions, with a predominance in pediatric patients. In adults, there has been an average age of onset at 50 years with a female predominance in a 1:7 with respect to the men [3]. An estimated worldwide incidence of 1.2 cases per million inhabitants. In Latin America, there is no standardized report that allows establishing epidemiological data, with an estimated survival of 38% one year after diagnosis [4] (Figure 1). However, this figure may be underestimated as it is a diagnosis of exclusion and due to the lack of specificity of the clinical picture.