Childhood supratentorial ependymomas with YAP1‐MAMLD1 fusion: an entity with characteristic clinical, radiological, cytogenetic and histopathological features

Ependymoma with YAP1‐MAMLD1 fusion is a rare, recently described supratentorial neoplasm of childhood, with few cases published so far. We report on 15 pediatric patients with ependymomas carrying YAP1‐MAMLD1 fusions, with their characteristic histopathology, immunophenotype and molecular/cytogeneti...

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Autores principales: Andreiuolo, Felipe, Varlet, Pascale, Tauziède‐Espariat, Arnault, Jünger, Stephanie T., Dörner, Evelyn, Dreschmann, Verena, Kuchelmeister, Klaus, Waha, Andreas, Haberler, Christine, Slavc, Irene, Corbacioglu, Selim, Riemenschneider, Markus J., Leipold, Alfred, Rüdiger, Thomas, Körholz, Dieter, Acker, Till, Russo, Alexandra, Faber, Jörg, Sommer, Clemens, Armbrust, Sven, Rose, Martina, Erdlenbruch, Bernhard, Hans, Volkmar H., Bernbeck, Benedikt, Schneider, Dominik, Lorenzen, Johann, Ebinger, Martin, Handgretinger, Rupert, Neumann, Manuela, van Buiren, Miriam, Prinz, Marco, Roganovic, Jelena, Jakovcevic, Antonia, Park, Sung‐Hye, Grill, Jacques, Puget, Stéphanie, Messing‐Jünger, Martina, Reinhard, Harald, Bergmann, Markus, Hattingen, Elke, Pietsch, Torsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379249/
https://www.ncbi.nlm.nih.gov/pubmed/30246434
http://dx.doi.org/10.1111/bpa.12659

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