Literature DB >> 1377013

Trisomy 2 as the sole chromosomal abnormality in a hepatoblastoma.

G Bardi1, B Johansson, N Pandis, S Heim, N Mandahl, A Békássy, I Hägerstrand, F Mitelman.   

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.

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Year:  1992        PMID: 1377013     DOI: 10.1002/gcc.2870040111

Source DB:  PubMed          Journal:  Genes Chromosomes Cancer        ISSN: 1045-2257            Impact factor:   5.006


  2 in total

1.  Characterization of genomic alterations in hepatoblastomas. A role for gains on chromosomes 8q and 20 as predictors of poor outcome.

Authors:  R G Weber; T Pietsch; D von Schweinitz; P Lichter
Journal:  Am J Pathol       Date:  2000-08       Impact factor: 4.307

2.  Hepatic loss in a young patient: a very 'cold case'.

Authors:  Vincenzo De Francesco; Enzo Ierardi; Giuseppe Stoppino; Fabrizio Corsi; Maria Rosaria D'Agnessa; Michele Castriota; Cesare Hassan; Francesco Cianci; Angelo Zullo
Journal:  Intern Emerg Med       Date:  2011-03-23       Impact factor: 3.397

  2 in total

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