ATRT-21. RHABDOID PREDISPOSITION SYNDROME: REPORT OF MOLECULAR PROFILES AND TREATMENT APPROACH IN THREE CHILDREN WITH SYNCHRONOUS ATYPICAL TERATOID/RHABDOID TUMOR AND MALIGNANT RHABDOID TUMOR

BACKGROUND: Rhabdoid predisposition syndrome is characterized by germline alterations in SMARCB1 or SMARCA4, leading to synchronous or metachronous central nervous system (CNS) and extra-CNS rhabdoid tumors. Rare survivors have been reported to date. METHODS: We describe the molecular profiling and...

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Detalhes bibliográficos
Publicado no:Neuro Oncol
Main Authors: Shatara, Margaret, Gupta, Ajay, Arja, Mohamed H Abu, Conley, Suzanne E, Patel, Priyal, Boué, Daniel R, Pierson, Christopher R, Thomas, Diana L, Meyer, Erin K, Shah, Summit H, Jones, Jeremy, Martin, Lisa, McAllister, Aaron, Schieffer, Kathleen M, Varga, Elizabeth A, Leraas, Kristen, Lichtenberg, Tara, LaHaye, Stephanie, Miller, Katherine E, Magrini, Vincent, Wilson, Richard K, Cottrell, Catherine E, Mardis, Elaine R, Aldrink, Jennifer H, Auletta, Jeffery J, Pindrik, Jonathan, Leonard, Jeffrey R, Osorio, Diana S, Finlay, Jonathan L, Ranalli, Mark, AbdelBaki, Mohamed S
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2020
Assuntos:
Atypical Teratoid/Rhabdoid Tumors
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7715330/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/neuonc/noaa222.020
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