Karyotypic characterization of infant embryonal rhabdomyosarcoma

Cancer Genet Cytogenet. 2008 Jan 15;180(2):145-8. doi: 10.1016/j.cancergencyto.2007.09.020.

Abstract

Despite embryonal rhabdomyosarcoma (eRMS) representing the most frequent form of RMS, the karyotypic characterization of this tumor subtype is still incomplete. We report the karyotypic analysis of two new cases of infant-onset eRMS. Both cases had a hyperdiploid karyotype, including gain of chromosomes 2 and 8. Only one of the cases showed a structural aberration, an unbalanced rearrangement involving 4p. These cases, together with a review of the literature, suggest that a karyotypic subgroup exists in infant eRMS that is defined by hyperdiploidy (<53 chromosomes) and includes gain of chromosomes 2, 8, 11, and 17, with few or no structural aberrations. Hence, this report illustrates that distinct karyotypic subgroups may be found in eRMS, which ultimately may be shown to have prognostic relevance.

Publication types

  • Case Reports

MeSH terms

  • Chromosome Aberrations*
  • Eye Neoplasms / genetics*
  • Fatal Outcome
  • Humans
  • Infant
  • Karyotyping
  • Male
  • Prostatic Neoplasms / genetics*
  • Rhabdomyosarcoma, Embryonal / genetics*