{"title":"Correlation between morphology and immunophenotype in the diagnosis of pure erythroid leukemia","authors":"Ariel Raúl Aragón Abrantes, Liekna Elena Sosa Saez, Danelis Hernández Aguiar","doi":"10.15406/htij.2022.10.00288","DOIUrl":null,"url":null,"abstract":"Pure erythroid leukemia is a rare entity that represents less than 5% of pediatric acute myeloid leukemias and is classified according to the World Health Organization (WHO) within the group of unspecified acute leukemias. A clinical case of a 5-year-old patient admitted with septic arthritis in the Pediatric Hospital, he also presenting with fever and anemia, for which a medullogram and immunophenotype were performed and erythroleukemia was diagnosed. It can be concluded that it is necessary for its diagnosis to integrate clinical, morphological and immunophenotypic, genetic and molecular studies.","PeriodicalId":103294,"journal":{"name":"Hematology & Transfusion International Journal","volume":"228 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Hematology & Transfusion International Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15406/htij.2022.10.00288","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
Pure erythroid leukemia is a rare entity that represents less than 5% of pediatric acute myeloid leukemias and is classified according to the World Health Organization (WHO) within the group of unspecified acute leukemias. A clinical case of a 5-year-old patient admitted with septic arthritis in the Pediatric Hospital, he also presenting with fever and anemia, for which a medullogram and immunophenotype were performed and erythroleukemia was diagnosed. It can be concluded that it is necessary for its diagnosis to integrate clinical, morphological and immunophenotypic, genetic and molecular studies.