Trisomy 3 in two paediatric post-transplant lymphomas

Br J Haematol. 2002 Jun;117(3):558-62. doi: 10.1046/j.1365-2141.2002.03481.x.

Abstract

Few cytogenetic data are available concerning the chromosomal constitution of post-transplant lymphomas. We report two paediatric cases of trisomy 3, as a primary anomaly, in post-transplant lymphoproliferative disease (PTLD) associated with B immunophenotype. Using cytogenetic analysis and fluorescence in situ hybridization on chromosome preparations, we found trisomy 3 in both patients and an extra X chromosome in one. Clinical, histological and immunophenotypical data are presented. Trisomy 3 has been observed in different types of non-Hodgkin's lymphomas but it is relatively rare in B-cell lymphomas, with the exception of marginal zone lymphoma and mantle cell lymphoma. To our knowledge, trisomy 3 is an uncommon cytogenetic finding in PTLD. Further cytogenetic studies of these lymphoproliferative disorders might contribute to evaluate the role of these chromosomal anomalies in the pathogenesis of this disease.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Chromosomes, Human, Pair 3*
  • Herpesvirus 4, Human / isolation & purification
  • Humans
  • Infant
  • Karyotyping
  • Kidney Transplantation*
  • Liver Transplantation*
  • Lymphoma, B-Cell / genetics*
  • Lymphoma, B-Cell / virology
  • Male
  • Postoperative Complications
  • Trisomy*