A novel reciprocal (10;17)(p11.2;q23) in myxoid fibrosarcoma

Cancer Genet Cytogenet. 2001 Jan 15;124(2):144-6. doi: 10.1016/s0165-4608(00)00341-1.

Abstract

Recurring reciprocal translocations have been identified as the primary chromosome aberrations in a number of neoplasms. These aberrations are often closely associated with particular morphologic or phenotypic subtypes of tumors and in some cases have prognostic implications. We have identified a novel reciprocal t(10;17)(p11.2;q23) in a case of low-grade myxoid fibrosarcoma, which may prove to be a new tumor specific chromosome aberration.

Publication types

  • Case Reports

MeSH terms

  • Chromosomes, Human, Pair 10*
  • Chromosomes, Human, Pair 17*
  • Fibrosarcoma / genetics*
  • Fibrosarcoma / pathology*
  • Fibrosarcoma / surgery
  • Humans
  • Male
  • Middle Aged
  • Soft Tissue Neoplasms / genetics*
  • Soft Tissue Neoplasms / pathology*
  • Soft Tissue Neoplasms / surgery
  • Thigh / pathology
  • Thigh / surgery
  • Translocation, Genetic*