Successive transformation of chronic myelomonocytic leukaemia into acute myeloblastic then lymphoblastic leukaemia, both with minor-bcr rearrangement

Br J Haematol. 1997 Jul;98(1):210-2. doi: 10.1046/j.1365-2141.1997.1692986.x.

Abstract

We report a case of chronic myelomonocytic leukaemia (CMML), which transformed first into acute myeloblastic leukaemia (AML) and then into acute lymphoblastic leukaemia (ALL). In the AML and ALL phases, chromosome analysis showed a classic Philadelphia chromosome (Ph) t(9:22)(q34:q11). Molecular studies showed breakpoint cluster region rearrangement between exons e1 and a2 compatible with a p190(bcr/abl) breakpoint as observed in Ph-positive lymphoblastic acute leukaemia. The minor (m-bcr) rearrangement was also detected during complete remission. This observation supports a multistep pathogenesis of leukaemias, and that the p190(bcr/abl) breakpoint may influence the course of the disease.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Cell Transformation, Neoplastic
  • Chromosomes, Human, Pair 22
  • Chromosomes, Human, Pair 9
  • Disease Progression
  • Fusion Proteins, bcr-abl / genetics
  • Gene Rearrangement
  • Humans
  • Karyotyping
  • Leukemia, Myeloid, Acute / genetics
  • Leukemia, Myeloid, Acute / pathology*
  • Leukemia, Myelomonocytic, Chronic / genetics
  • Leukemia, Myelomonocytic, Chronic / pathology*
  • Male
  • Polymerase Chain Reaction
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / genetics
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / pathology*
  • Translocation, Genetic

Substances

  • Fusion Proteins, bcr-abl