Trisomy 2 as the sole chromosomal abnormality in a hepatoblastoma

Genes Chromosomes Cancer. 1992 Jan;4(1):78-80. doi: 10.1002/gcc.2870040111.

Abstract

Short-term cultures of a fine-needle aspirate from a hepatoblastoma were analyzed cytogenetically. Trisomy 2 was found as the sole abnormality, yielding the karyotype 47,XY, + 2/46,XY. Because trisomy for all or part of chromosome 2 has been described, although together with other aberrations, in seven of the 11 hepatoblastomas hitherto reported, the finding of + 2 as the only anomaly in the present case strongly indicates that additional chromosome 2 material is of pathogenetic significance in this tumor type.

Publication types

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

MeSH terms

  • Carcinoma, Hepatocellular / genetics*
  • Carcinoma, Hepatocellular / pathology
  • Chromosomes, Human, Pair 2*
  • Humans
  • Infant
  • Liver Neoplasms / genetics*
  • Liver Neoplasms / pathology
  • Male
  • Trisomy*