Literature DB >> 12550761

Spindle-cell rhabdomyosarcoma with 2q36 approximately q37 involvement.

Maria Debiec-Rychter1, Anne Hagemeijer, Raf Sciot.   

Abstract

The cytogenetic analysis of a spindle-cell variant of embryonal rhabdomyosarcoma (RMS), presenting as a cheek mass in an 18-year-old girl, is reported. The tumor cells showed an abnormal karyotype 46,XX,der(2)t(2;7)(q36 approximately q37;q3?),del(14)(q24),der(16)t(1;16)(q21;q13), with a tetraploid range of chromosome number in a subpopulation of cells. By fluorescence in situ hybridization analysis, the tumor cells were negative for FKHR-disrupting translocations specific for alveolar type of RMS and for NMYC gene amplification.

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Year:  2003        PMID: 12550761     DOI: 10.1016/s0165-4608(02)00647-7

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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