Complex translocation involving Ph chromosome in a patient with typical chronic myelogenous leukemia

Cancer Genet Cytogenet. 1992 Oct 1;63(1):52-5. doi: 10.1016/0165-4608(92)90064-f.

Abstract

We report a cytogenetic study of a patient with chronic myelogenous leukemia (CML) who, while displaying a Philadelphia (Ph) chromosome, resulting from a standard t(9;22) at diagnosis, during the chronic phase (CP) showed disappearance of the Ph and occurrence of new chromosome changes, including a marker probably arising from a translocation involving chromosome 17 and the Ph. In situ hybridization confirmed the cytogenetic appearance and demonstrated that the breakpoint on the Ph marker occurred below the BCR-ABL fusion gene.

Publication types

  • Case Reports

MeSH terms

  • Chromosome Deletion
  • Chromosomes, Human, Pair 17*
  • Chromosomes, Human, Pair 18
  • Chromosomes, Human, Pair 7
  • Chromosomes, Human, Pair 9
  • Female
  • Humans
  • In Situ Hybridization
  • Leukemia, Myeloid, Chronic-Phase / genetics*
  • Microscopy, Fluorescence
  • Middle Aged
  • Philadelphia Chromosome*
  • Translocation, Genetic*