Two distinct genetically defined entities of ependymoma arising in the supratentorial compartment are characterized by the presence of either a C11orf95-RELA or a YAP-MAMLD1 fusion, respectively. There is growing evidence that supratentorial ependymomas without these genetic features exist. In this study, we report on 18 pediatric non-RELA/non-YAP supratentorial ependymomas that were systematically characterized by means of their histology, immunophenotype, genetics, and epigenomics. Comprehensive molecular analyses included high-resolution copy number analysis, methylation profiling, analysis of fusion transcripts by Nanostring technology, and RNA sequencing. Based upon histological and immunohistochemical features two main patterns were i...
We have previously identified two ALK rearrangements in a subset of ependymal tumors using a combina...
Ependymal tumors across age groups are currently classified and graded solely by histopathology. It ...
Pediatric ependymomas are enigmatic tumors that continue to present a clinical management challenge ...
Abstract Extensive molecular analyses of ependymal tumors have revealed that supratentorial and post...
Ependymoma with YAP1-MAMLD1 fusion is a rare, recently described supratentorial neoplasm of childhoo...
Ependymomas (EPs) are tumors of the brain and spinal cord constituting ∼10% of the childhood central...
Ependymomas encompass a heterogeneous group of central nervous system (CNS) neoplasms that occur alo...
Ependymomas are glial neoplasms with a wide morphological spectrum. The majority of supratentorial e...
Abstract The cIMPACT-NOW Update 7 has replaced the WHO nosology of “ependymoma, RELA fusion positive...
International audienceClear cell ependymoma is one of the 4 main histological subtypes of ependymoma...
Introduction: Young age is an adverse prognostic factor in children with ependymomas. Treatment of t...
International audienceMolecular groups of supratentorial ependymomas comprise tumors with ZFTA-RELA ...
Ependymal tumors across age groups are currently classified and graded solely by histopathology. It ...
Pediatric ependymomas are enigmatic tumors that continue to present a clinical management challenge ...
Molecular groups of supratentorial ependymomas comprise tumors with ZFTA-RELA or YAP1-involving fusi...
We have previously identified two ALK rearrangements in a subset of ependymal tumors using a combina...
Ependymal tumors across age groups are currently classified and graded solely by histopathology. It ...
Pediatric ependymomas are enigmatic tumors that continue to present a clinical management challenge ...
Abstract Extensive molecular analyses of ependymal tumors have revealed that supratentorial and post...
Ependymoma with YAP1-MAMLD1 fusion is a rare, recently described supratentorial neoplasm of childhoo...
Ependymomas (EPs) are tumors of the brain and spinal cord constituting ∼10% of the childhood central...
Ependymomas encompass a heterogeneous group of central nervous system (CNS) neoplasms that occur alo...
Ependymomas are glial neoplasms with a wide morphological spectrum. The majority of supratentorial e...
Abstract The cIMPACT-NOW Update 7 has replaced the WHO nosology of “ependymoma, RELA fusion positive...
International audienceClear cell ependymoma is one of the 4 main histological subtypes of ependymoma...
Introduction: Young age is an adverse prognostic factor in children with ependymomas. Treatment of t...
International audienceMolecular groups of supratentorial ependymomas comprise tumors with ZFTA-RELA ...
Ependymal tumors across age groups are currently classified and graded solely by histopathology. It ...
Pediatric ependymomas are enigmatic tumors that continue to present a clinical management challenge ...
Molecular groups of supratentorial ependymomas comprise tumors with ZFTA-RELA or YAP1-involving fusi...
We have previously identified two ALK rearrangements in a subset of ependymal tumors using a combina...
Ependymal tumors across age groups are currently classified and graded solely by histopathology. It ...
Pediatric ependymomas are enigmatic tumors that continue to present a clinical management challenge ...