Spindle-cell rhabdomyosarcoma with 2q36 approximately q37 involvement

Cancer Genet Cytogenet. 2003 Jan 1;140(1):62-5. doi: 10.1016/s0165-4608(02)00647-7.

Abstract

The cytogenetic analysis of a spindle-cell variant of embryonal rhabdomyosarcoma (RMS), presenting as a cheek mass in an 18-year-old girl, is reported. The tumor cells showed an abnormal karyotype 46,XX,der(2)t(2;7)(q36 approximately q37;q3?),del(14)(q24),der(16)t(1;16)(q21;q13), with a tetraploid range of chromosome number in a subpopulation of cells. By fluorescence in situ hybridization analysis, the tumor cells were negative for FKHR-disrupting translocations specific for alveolar type of RMS and for NMYC gene amplification.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Cheek*
  • Chromosome Deletion
  • Chromosome Painting
  • Chromosomes, Human, Pair 14
  • Chromosomes, Human, Pair 16 / genetics
  • Chromosomes, Human, Pair 16 / ultrastructure
  • Chromosomes, Human, Pair 2 / genetics
  • Chromosomes, Human, Pair 2 / ultrastructure*
  • Chromosomes, Human, Pair 7 / genetics
  • Chromosomes, Human, Pair 7 / ultrastructure
  • Diploidy
  • Facial Neoplasms / genetics*
  • Female
  • Humans
  • Rhabdomyosarcoma, Embryonal / genetics*
  • Translocation, Genetic*