A Molecular Study of Pediatric Spindle and Sclerosing Rhabdomyosarcoma: Identification of Novel and Recurrent VGLL2-Related Fusions in Infantile Cases

Sclerosing and spindle cell rhabdomyosarcoma (SRMS) have been recently re-classified as a stand-alone pathologic entity, separate from embryonal RMS (ERMS). Genetically a subset of the congenital cases display NCOA2 gene rearrangements, while tumors occurring in older children or adults harbor MYOD1...

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Detalhes bibliográficos
Publicado no:Am J Surg Pathol
Main Authors: Alaggio, Rita, Zhang, Lei, Sung, Yun-Shao, Huang, Shih-Chiang, Chen, Chun-Liang, Bisogno, Gianni, Zin, Angelica, Agaram, Narasimhan P, LaQuaglia, Michael P., Wexler, Leonard H., Antonescu, Cristina R
Formato: Artigo
Idioma:Inglês
Publicado em: 2016
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4712098/
https://ncbi.nlm.nih.gov/pubmed/26501226
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/PAS.0000000000000538
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