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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Détails bibliographiques
Publié dans:Neuro Oncol
Auteurs principaux: 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
Format: Artigo
Langue:Inglês
Publié: Oxford University Press 2020
Sujets:
Atypical Teratoid/Rhabdoid Tumors
Accès en ligne: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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