t(12;22)(q13;q13) and trisomy 8 are nonrandom aberrations in clear-cell sarcoma

Cancer Genet Cytogenet. 1992 Dec;64(2):107-10. doi: 10.1016/0165-4608(92)90338-9.

Abstract

We report a case of clear-cell sarcoma with a t(12;22)(q13;q13) and multiple copies of chromosome 8 in addition to other abnormalities. An identical or similar translocation has previously been reported in this type of tumor, suggesting that the t(12;22) is a primary cytogenetic change in the pathogenesis of a subset of clear-cell sarcomas. In addition, the presence of extra copies of chromosome 8, commonly noted in our case and others, suggests that it represents a nonrandom secondary change in these tumors.

Publication types

  • Case Reports

MeSH terms

  • Chromosome Aberrations*
  • Chromosomes, Human, Pair 12*
  • Chromosomes, Human, Pair 22*
  • Chromosomes, Human, Pair 8*
  • Humans
  • Karyotyping
  • Lymphatic Metastasis
  • Male
  • Middle Aged
  • Sarcoma / genetics*
  • Sarcoma / pathology
  • Soft Tissue Neoplasms / genetics*
  • Testicular Neoplasms / genetics*
  • Testicular Neoplasms / surgery
  • Translocation, Genetic
  • Trisomy