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

Andreiuolo, Felipe; Varlet, Pascale; Tauziède‐Espariat, Arnault; T. Jünger, Stephanie; Dörner, Evelyn; Dreschmann, Verena; Kuchelmeister, K.; Waha, Andreas; Haberler, Christine; Slavc, Irene; Corbacioglu, Selim; J. Riemenschneider, Markus; Leipold, Alfred; Rüdiger, Thomas; Körholz, Dieter; Acker, Till; Russo, Alexandra; Faber, Jörg; Sommer, Clemens; Armbrust, Sven; Rose, Martina; Erdlenbruch, Bernhard; Hans, Volkmar; Bernbeck, Benedikt; T. Schneider, Dominik; Lorenzen, Johann; Ebinger, Martin; Handgretinger, Rupert; Neumann, Manuela; van Buiren, Miriam; Prinz, Marco; Roganović, Jelena; Jakovčević, Antonia; Park, Sung‐Hye; Grill, Jacques; Puget, Stéphanie; Messing‐Jünger, Martina; Reinhard, Harald; Bergmann, Markus; Hattingen, Elke; Pietsch, Torsten

doi:10.1111/bpa.12659

Public

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

Published in Brain Pathology • Sep 24, 2018

Authors:

Felipe Andreiuolo

Pascale Varlet

Arnault Tauziède‐Espariat

Abstract

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...

Subject

Ependymoma

Pathology

Biology

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