Ependymomas are rare central nervous system tumours that can arise in the brain's
supratentorial region or posterior fossa, or in the spinal cord. In 1924, Percival Bailey …

Pediatric neoplasms in the central nervous system (CNS) are the leading cause of cancer-
related deaths in children. Recent developments in molecular analyses have greatly …

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 …

Molecular groups of supratentorial ependymomas comprise tumors with ZFTA–RELA or
YAP1-involving fusions and fusion-negative subependymoma. However, occasionally …

Sclerosing epithelioid fibrosarcoma (SEF) is an aggressive soft tissue sarcoma,
characterized by a distinctive epithelioid phenotype in a densely sclerotic collagenous …

Although ependymomas (EPNs) have similar histopathology, they are heterogeneous
tumors with diverse immunophenotypes, genetics, epigenetics, and different clinical …

Recurrent fusion genes involving C11orf95, C11orf95‐RELA, have been identified only in
supratentorial ependymomas among primary CNS tumors. Here, we report hitherto …

Simple Summary The current trend in neuropathology directs to the integrated histo-
molecular approach. The traditional concept of histological grade should be complemented …

Ependymomas are primary central nervous system tumors (CNS), arising within the
posterior fossa and supratentorial regions of the brain, and in the spine. Over the last …

Although ependymoma (EPN) molecular subgroups have been well established by
integrated high-throughput platforms, low-and middle-income countries still need low-cost …