Recurrent unbalanced whole-arm t(1;10)(q10;p10) in myelodysplastic syndrome: a case report and literature review

Cancer Genet Cytogenet. 2007 Jan 15;172(2):165-7. doi: 10.1016/j.cancergencyto.2006.09.022.

Abstract

We report a patient with myelodysplastic syndrome (refractory anemia) showing the karyotype 46,XY,+1,der(1;10)(q10;p10), resulting in trisomy 1q and monosomy 10q abnormality. This finding suggests that either trisomy of 1q or centromeric connection between chromosomes 1 and 10, rather than the absence of 10q, might be essential toward neoplastic transformation.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Allelic Imbalance
  • Chromosomes, Human, Pair 1 / genetics*
  • Chromosomes, Human, Pair 10 / genetics*
  • Humans
  • Male
  • Middle Aged
  • Myelodysplastic Syndromes / genetics*
  • Neoplasm Recurrence, Local / genetics*
  • Translocation, Genetic*