| Literature DB >> 16424389 |
Ilske Oschlies1, Wolfram Klapper, Martin Zimmermann, Matthias Krams, Hans-Heinrich Wacker, Birgit Burkhardt, Lana Harder, Reiner Siebert, Alfred Reiter, Reza Parwaresch.
Abstract
Diffuse large B-cell lymphoma (DLBCL) in adults is a heterogeneous disease. Biologic subgroups of DLBCL with a favorable prognosis (germinal center B-cell-like, GCB) and with a poor prognosis (activated B-cell-like, ABC) have been defined by gene expression profiling and can be distinguished by immunohistochemistry. In contrast to their adult counterparts, children with DLBCL have an excellent prognosis. We analyzed 63 cases of DLBCL in pediatric patients by immunohistochemistry and fluorescence in situ hybridization (FISH) and found a striking predominance of a GCB subtype, which might explain the good clinical outcome in these lymphomas. Interestingly, FISH applied to 50 of these cases, as well as conventional cytogenetics available in 3 cases, revealed absence of the translocation t(14;18) involving the BCL2 gene, which is present in about 15% of adult GCB subtype DLBCL. Our data indicate that pediatric DLBCL differs from adult DLBCL and might comprise a biologically unique subgroup of DLBCL from which important insights into the pathogenesis and biology of this disease might be gained.Entities:
Mesh:
Year: 2006 PMID: 16424389 DOI: 10.1182/blood-2005-10-4213
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113