Atypical cytogenic aberrations in two childhood peripheral primitive neuroectodermal tumors

Genes Chromosomes Cancer. 1995 Feb;12(2):142-7. doi: 10.1002/gcc.2870120209.

Abstract

Atypical cytogenetic abnormalities were detected in peripheral primitive neuroectodermal tumors (PPNET) of the extremity in two children. One had an osseous tumor with a balanced reciprocal translocation, t(5;9)(q22;q32), and had a complete response to therapy. The other had a non-osseous tumor with an interstitial deletion, del(18)(q12.2q21.2), was resistant to combination therapy, and at autopsy had evidence of possible clonal evolution with the karyotype 46,XX der(8)t(8;8)(p11.2;q13), inv(16)(p13.2q12),del(18)(q12.2q21.2). Neither tumor demonstrated the t(11;22)(q24;q12) typically found in Ewing's sarcoma and PPNET, suggesting heterogeneity of the cytogenetic aberrations seen in this rare childhood malignancy.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bone Neoplasms / genetics*
  • Child
  • Chromosome Aberrations*
  • Female
  • Humans
  • Karyotyping
  • Male
  • Neuroectodermal Tumors, Primitive, Peripheral / genetics*
  • Soft Tissue Neoplasms / genetics*