Case report: long-term survival of an infant syndromic patient affected by atypical teratoid-rhabdoid tumor

BACKGROUND: Atypical teratoid rhabdoid tumor (ATRT) patients display a dismal median overall survival of less than 1 year. A consistent fraction of cases carries de-novo SMARCB1/INI1 constitutional mutations in the setting of the “rhabdoid tumor predisposition syndrome” and the outcome is worst in i...

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Detalles Bibliográficos
Autores principales: Modena, Piergiorgio, Sardi, Iacopo, Brenca, Monica, Giunti, Laura, Buccoliero, Anna Maria, Pollo, Bianca, Biassoni, Veronica, Genitori, Lorenzo, Antonelli, Manila, Maestro, Roberta, Giangaspero, Felice, Massimino, Maura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3600022/
https://www.ncbi.nlm.nih.gov/pubmed/23510391
http://dx.doi.org/10.1186/1471-2407-13-100

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3600022/
https://www.ncbi.nlm.nih.gov/pubmed/23510391
http://dx.doi.org/10.1186/1471-2407-13-100

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