t(X;17) as the sole karyotypic anomaly in a case of M(3r) subtype of acute promyelocytic leukemia without RARalpha rearrangement

Leuk Res. 2010 Feb;34(2):e55-7. doi: 10.1016/j.leukres.2009.04.034. Epub 2009 May 27.

Abstract

We describe here a unique chromosomal abnormality found in a patient with M(3r) subtype of APL. Neither t(15;17) nor rearrangement of RARalpha was detected by routine R-banded chromosome as well as fluorescence in situ hybridization (FISH) analysis using PML/RARalpha dual-color dual-fusion translocation probe and RARalpha dual-color break apart rearrangement probe. Instead of the typical rearrangement between chromosomes 15 and 17, all cells analyzed had a translocation between X and 17 as the sole karyotypic anomaly. The translocation was conformed by whole chromosome painting (WCP) with painting probes of chromosomes X and 17. To our knowledge, this is the first documented APL with a novel translocation involving chromosomes X and 17 without RARalpha gene rearrangement.

Publication types

  • Letter

MeSH terms

  • Chromosomes, Human, Pair 17*
  • Chromosomes, Human, X*
  • Humans
  • Karyotyping
  • Leukemia, Promyelocytic, Acute / classification
  • Leukemia, Promyelocytic, Acute / genetics*
  • Receptors, Retinoic Acid / genetics*
  • Retinoic Acid Receptor alpha
  • Translocation, Genetic*

Substances

  • RARA protein, human
  • Receptors, Retinoic Acid
  • Retinoic Acid Receptor alpha