A t(1;9)(q10;q10) translocation with additional 6q23 and 9q22 rearrangements in a case of chondromyxoid fibroma

Tahereh Dadfarnia, Gopalrao V.N. Velagaleti, Kelly D. Carmichael, Eduardo Eyzaguirre, Mahmoud A. Eltorky, Suimin Qiu

Producción científica: Articlerevisión exhaustiva

2 Citas (Scopus)

Resumen

Chondromyxoid fibroma (CMF) is a rare cartilaginous tumor of bone. It typically presents in the long tubular bones and to a lesser extent in the small bones of the hands and feet of young adults. To date, several cytogenetic abnormalities have been described in association with CMF. We studied a phalangeal CMF from a 13-year-old female by cytogenetic methods. We found a novel unbalanced translocation between the long arms of chromosomes 1 and 9, resulting in loss of 1p. In addition, rearrangements involving the 6q23 and 9q22 regions were also observed. To our knowledge, this is the first report in the literature describing this novel chromosomal translocation in CMF.

Idioma originalEnglish (US)
Páginas (desde-hasta)666-670
Número de páginas5
PublicaciónCancer Genetics
Volumen204
N.º12
DOI
EstadoPublished - dic 2011
Publicado de forma externa

ASJC Scopus subject areas

  • Genetics
  • Molecular Biology
  • Cancer Research

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Profundice en los temas de investigación de 'A t(1;9)(q10;q10) translocation with additional 6q23 and 9q22 rearrangements in a case of chondromyxoid fibroma'. En conjunto forman una huella única.

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