Cribriform neuroepithelial tumor: molecular characterization of a SMARCB1‐deficient non‐rhabdoid tumor with favorable long‐term outcome

Rhabdoid phenotype and loss of SMARCB1 expression in a brain tumor are characteristic features of atypical teratoid/rhabdoid tumors (ATRT). Rare non‐rhabdoid brain tumors showing cribriform growth pattern and SMARCB1 loss have been designated cribriform neuroepithelial tumor (CRINET). Small case ser...

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Veröffentlicht in:	Brain pathology (Zurich, Switzerland) Switzerland), 2017-07, Vol.27 (4), p.411-418
Hauptverfasser:	Johann, Pascal D., Hovestadt, Volker, Thomas, Christian, Jeibmann, Astrid, Heß, Katharina, Bens, Susanne, Oyen, Florian, Hawkins, Cynthia, Pierson, Christopher R., Aldape, Kenneth, Kim, Sang‐Pyo, Widing, Eva, Sumerauer, David, Hauser, Péter, van Landeghem, Frank, Ryzhova, Marina, Korshunov, Andrey, Capper, David, Jones, David T.W., Pfister, Stefan M., Schneppenheim, Reinhard, Siebert, Reiner, Paulus, Werner, Frühwald, Michael C., Kool, Marcel, Hasselblatt, Martin
Format:	Artikel
Sprache:	eng
Schlagworte:	Age Analogies Arrays atypical teratoid/rhabdoid tumor Brain Brain Neoplasms - genetics Brain tumors Child Child, Preschool Children Cluster analysis Clusters copy number alterations Data processing DNA Methylation - genetics DNA methylation profiling Female Fish Girls Humans Infant Kaplan-Meier Estimate Male Medical prognosis Methylation Mutation Mutation - genetics Myc protein Neoplasms, Neuroepithelial - genetics Neoplasms, Neuroepithelial - pathology Patients Prognosis Rhabdoid Tumor - genetics Rhabdoid Tumor - pathology Sequences SMARCB1 Protein - deficiency SMARCB1 Protein - genetics SMARCB1/INI1 Staining Statistics, Nonparametric Subgroups Survival Tumors Tyrosinase
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