Please use this identifier to cite or link to this item: https://doi.org/10.1111/bjh.12042
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dc.titleThe immunophenotype of T-lymphoblastic lymphoma in children and adolescents: A children's oncology group report
dc.contributor.authorPatel, J.L.
dc.contributor.authorSmith, L.M.
dc.contributor.authorAnderson, J.
dc.contributor.authorAbromowitch, M.
dc.contributor.authorCampana, D.
dc.contributor.authorJacobsen, J.
dc.contributor.authorLones, M.A.
dc.contributor.authorGross, T.G.
dc.contributor.authorCairo, M.S.
dc.contributor.authorPerkins, S.L.
dc.date.accessioned2016-07-08T09:29:19Z
dc.date.available2016-07-08T09:29:19Z
dc.date.issued2012-11
dc.identifier.citationPatel, J.L., Smith, L.M., Anderson, J., Abromowitch, M., Campana, D., Jacobsen, J., Lones, M.A., Gross, T.G., Cairo, M.S., Perkins, S.L. (2012-11). The immunophenotype of T-lymphoblastic lymphoma in children and adolescents: A children's oncology group report. British Journal of Haematology 159 (4) : 454-461. ScholarBank@NUS Repository. https://doi.org/10.1111/bjh.12042
dc.identifier.issn00071048
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/125616
dc.description.abstractT-lymphoblastic leukaemia (T-ALL) and T-lymphoblastic lymphoma (T-LBL) are neoplasms derived from immature lymphoid cells of T-cell lineage. These neoplasms are biologically similar, but significant differences may exist between the two given their clinical differences. Although ample data regarding the immunophenotypic characterization T-ALL are available, there is a paucity of such data in children and adolescents with T-LBL. We used flow cytometry and/or immunohistochemistry to characterize the immunophenotypic profile of 180 children and adolescents with newly diagnosed T-LBL enrolled in the Children's Oncology Group 5971 study. Multiple T-cell, B-cell, myeloid, and other markers were evaluated. We identified diagnostically useful immunophenotypic features of T-LBL as well as distinct immunophenotypic subgroups, although none of these was statistically related to event-free or overall survival in this retrospective analysis. Further studies of biologically and immunophenotypically distinct subgroups of T-LBL, such as the early T-cell precursor phenotype, are warranted. © 2012 Blackwell Publishing Ltd.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1111/bjh.12042
dc.sourceScopus
dc.subjectEarly T-cell precursor
dc.subjectImmunophenotypic analysis
dc.subjectPaediatric lymphoma
dc.subjectT-cell antigens
dc.subjectT-lymphoblastic lymphoma
dc.typeArticle
dc.contributor.departmentPAEDIATRICS
dc.description.doi10.1111/bjh.12042
dc.description.sourcetitleBritish Journal of Haematology
dc.description.volume159
dc.description.issue4
dc.description.page454-461
dc.description.codenBJHEA
dc.identifier.isiut000310485400009
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