A novel translocation (17;19)(p13;p13) in a patient with acute myelomonocytic leukemia

Cancer Genet Cytogenet. 2000 May;119(1):77-9. doi: 10.1016/s0165-4608(99)00214-9.

Abstract

We report on a patient with acute myeloid leukemia (AML M4) and a so far unrecorded translocation (17;19). The leukemia transformed from a myeloproliferative disorder (MPD) and showed a progressive fatal course. Following transformation, all leukemic cells showed an apparently balanced translocation (17;19)(p13;p13). The breakpoint regions harbor genes such as TP53 (17p13) and E2A, ENL, or LYL1 (19p13), which could be relevant in leukemogenesis. We suspect that the translocation (17;19)(p13;p13) may be a prognostic factor for transformation from chronic MPD to acute leukemia.

Publication types

  • Case Reports

MeSH terms

  • Chromosome Banding
  • Chromosomes, Human, Pair 17*
  • Chromosomes, Human, Pair 19*
  • Humans
  • Immunophenotyping
  • Karyotyping
  • Leukemia, Myelomonocytic, Acute / genetics*
  • Leukemia, Myelomonocytic, Acute / immunology
  • Male
  • Middle Aged
  • Translocation, Genetic*