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Provedor de dados:  BJMBR
País:  Brazil
Título:  Cytogenetic studies of Brazilian pediatric myelodysplastic syndrome cases: challenges and difficulties in a large and emerging country
Autores:  Velloso,E.D.R.P.
Chauffaille,M.L.
Peliçario,L.M.
Tanizawa,R.S.S.
Toledo,S.R.C.
Gaiolla,R.D.
Lopes,L.F.
Data:  2013-01-01
Ano:  2013
Palavras-chave:  Childhood myelodysplastic syndromes
Juvenile myelomonocytic leukemia
Cytogenetics
Karyotype
Diagnosis
Resumo:  Myelodysplastic syndromes (MDS) and juvenile myelomonocytic leukemia (JMML) are rare hematopoietic stem cell diseases affecting children. Cytogenetics plays an important role in the diagnosis of these diseases. We report here the experience of the Cytogenetic Subcommittee of the Brazilian Cooperative Group on Pediatric Myelodysplastic Syndromes (BCG-MDS-PED). We analyzed 168 cytogenetic studies performed in 23 different cytogenetic centers; 84 of these studies were performed in patients with confirmed MDS (primary MDS, secondary MDS, JMML, and acute myeloid leukemia/MDS+Down syndrome). Clonal abnormalities were found in 36.9% of the MDS cases and cytogenetic studies were important for the detection of constitutional diseases and for differential diagnosis with other myeloid neoplasms. These data show the importance of the Cooperative Group for continuing education in order to avoid a late or wrong diagnosis.
Tipo:  Info:eu-repo/semantics/article
Idioma:  Inglês
Identificador:  http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2013000100085
Editor:  Associação Brasileira de Divulgação Científica
Relação:  10.1590/1414-431X20122449
Formato:  text/html
Fonte:  Brazilian Journal of Medical and Biological Research v.46 n.1 2013
Direitos:  info:eu-repo/semantics/openAccess
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