Literature DB >> 10087951

Cytogenetic study of a spindle-cell rhabdomyosarcoma of the parotid gland.

R Gil-Benso1, C Carda-Batalla, S Navarro-Fos, A Pellín-Perez, A Llombart-Bosch.   

Abstract

The cytogenetic analysis of a spindle-cell rhabdomyosarcoma of the parotid gland in a 6-year-old boy is reported. The tumor cells showed an abnormal karyotype with a hypotriploid modal chromosome number and clonal structural rearrangements affecting chromosomes 1, 8, 12, 21, and 22. The tumor karyotype was: 59, XY, -1, -3, -4, -5, -6, +8, +8, +del(8)(q22q24), -9, -10, del(12)(q13), -15, -16, -17, -18, der(21)t(12;21)(p11;p11), -22, der(22)t(1;22)(q12;p11).

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Year:  1999        PMID： 10087951     DOI： 10.1016/s0165-4608(98)00163-0

Source DB:  PubMed          Journal:  Cancer Genet Cytogenet        ISSN： 0165-4608


  3 in total

1.  Cytogenetic and Molecular Study of an Adult Sclerosing Rhabdomyosarcoma of the Extremity: MYOD1-mutation and Clonal Evolution.

Authors:  Ludmila Gorunova; Bodil Bjerkehagen; Francesca Micci; Sverre Heim; Ioannis Panagopoulos
Journal:  Cancer Genomics Proteomics       Date:  2020 Sep-Oct       Impact factor: 4.069

2.  Recurrent NCOA2 gene rearrangements in congenital/infantile spindle cell rhabdomyosarcoma.

Authors:  Juan Miguel Mosquera; Andrea Sboner; Lei Zhang; Naoki Kitabayashi; Chun-Liang Chen; Yun Shao Sung; Leonard H Wexler; Michael P LaQuaglia; Morris Edelman; Chandrika Sreekantaiah; Mark A Rubin; Cristina R Antonescu
Journal:  Genes Chromosomes Cancer       Date:  2013-03-05       Impact factor: 5.006

3.  Recurrent MYOD1 mutations in pediatric and adult sclerosing and spindle cell rhabdomyosarcomas: evidence for a common pathogenesis.

Authors:  Narasimhan P Agaram; Chun-Liang Chen; Lei Zhang; Michael P LaQuaglia; Leonard Wexler; Cristina R Antonescu
Journal:  Genes Chromosomes Cancer       Date:  2014-05-14       Impact factor: 5.006
  3 in total

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