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Immunophenotypic characterization of acute leukemias in Bahia, Brazil

To characterize the immunophenotypic profile of acute leukemias in the population of the state of Bahia, Brazil. This is a descriptive, retrospective study. From 2014 to 2018, 796 new cases of acute leukemia were evaluated. The data were obtained from analysis of reports and records of tests perform...

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Bibliographic Details
Published in:Einstein (São Paulo, Brazil) Brazil), 2023, Vol.21, p.eAO0117-eAO0117
Main Authors: Santos, Mariane Melo Dos, Santos, Allan Souza Dos, Santos, Herbert Henrique de Melo, Santos, Lorene da Silva, Nascimento, Roberto José Meyer, Torres, Alex José Leite
Format: Article
Language:English
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Summary:To characterize the immunophenotypic profile of acute leukemias in the population of the state of Bahia, Brazil. This is a descriptive, retrospective study. From 2014 to 2018, 796 new cases of acute leukemia were evaluated. The data were obtained from analysis of reports and records of tests performed by flow cytometry immunophenotyping. All individuals of all age groups diagnosed as acute lymphoblastic leukemia or acute myeloid leukemia were included in the study. Demographic variables and expression of leukemia antigens were evaluated. Most cases were diagnosed as acute myeloid leukemia and 42.7% as acute lymphoblastic leukemia. Significant differences were found in expression of markers in acute leukemias when age groups were compared, as well as in demographic characteristics. B-cell acute lymphoblastic leukemia was more prevalent than cases of T-cell origin. Assessing the aberrant markers in acute myeloid leukemias, the non-acute promyelocytic leukemia group presented expression of CD7 and CD56 as the most frequent ones. In B-cell acute lymphoblastic leukemia, the most frequent aberrant markers were CD66c, CD13 and CD33. Significant differences were found as to several antigens when comparing adults and children, and these findings may contribute to future studies correlating the phenotypic profile to genetic characteristics and therapeutic response, including specific antigen therapies, which may be better targeted.
ISSN:1679-4508
2317-6385
2317-6385
DOI:10.31744/einstein_journal/2023AO0117