Literature DB >> 8242599

Two Down syndrome patients with an acquired translocation, t(8;14)(q11;q32), in early B-lineage acute lymphoblastic leukemia.

L M Secker-Walker1, J M Hawkins, H G Prentice, P H Mackie, N A Heerema, A J Provisor.   

Abstract

Two males with Down syndrome and acute lymphoblastic leukemia with the acquired translocation, t(8;14)(q11;q32), are described. In each case the constitutional karyotype was 47,XY,+21. The patients were, respectively, aged 3 years 11 months and 32 years, with presenting white blood counts 34 and 1.9 x 10(9)/L with blasts of FAB L1 and L2. In each case immunophenotype of the blasts was C-ALL. The child is alive and well and in first remission 6 years from diagnosis. In contrast, the adult patient died in first remission 8.5 months from diagnosis with severe pancytopenia. These are to our knowledge the second and third cases of ALL with t(8;14)(q11-12;q32) associated with a constitutional genetic disorder.

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Year:  1993        PMID: 8242599     DOI: 10.1016/0165-4608(93)90189-s

Source DB:  PubMed          Journal:  Cancer Genet Cytogenet        ISSN: 0165-4608


  2 in total

1.  Pediatric acute lymphoblastic leukemia with a t(8;14)(q11.2;q32): B-cell disease with a high proportion of Down syndrome: a Children's Oncology Group study.

Authors:  Yoav H Messinger; Rodney R Higgins; Meenakshi Devidas; Stephen P Hunger; Andrew J Carroll; Nyla A Heerema
Journal:  Cancer Genet       Date:  2012-09

2.  Clinical and genetic features of pediatric acute lymphoblastic leukemia in Down syndrome in the Nordic countries.

Authors:  Catarina Lundin; Erik Forestier; Mette Klarskov Andersen; Kirsi Autio; Gisela Barbany; Lucia Cavelier; Irina Golovleva; Sverre Heim; Kristiina Heinonen; Randi Hovland; Johann H Johannsson; Eigil Kjeldsen; Ann Nordgren; Lars Palmqvist; Bertil Johansson
Journal:  J Hematol Oncol       Date:  2014-04-11       Impact factor: 17.388

  2 in total

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