Abstract
The combination of ependymoma and gliosarcoma elements in the same tumor is extremely rare, and the molecular characteristics of these entities are not clear. Here, we present a rare aggressive brain tumor in a 12-year-old boy harboring a ZFTA::RELA gene fusion, a characteristic feature of supratentorial ependymomas. On the other hand, the histopathological, molecular, and methylation profiles were compatible with a diagnosis of a mesenchymal type, IDH wild-type glioblastoma multiforme (GBM). Additional somatic alterations provide evidence of RAS/MAPK signaling pathway activation. Overall, this report highlights the histopathological and molecular characteristics of a rare and aggressive glial tumor.
| Original language | English |
|---|---|
| Pages (from-to) | 1450-1453 |
| Number of pages | 4 |
| Journal | International Journal of Surgical Pathology |
| Volume | 33 |
| Issue number | 6 |
| DOIs | |
| State | Published - 1 Sep 2025 |
| Externally published | Yes |
Keywords
- C11orf95::RELA
- Gliosarcoma
- ZFTA::RELA
- ependymosarcoma
ASJC Scopus subject areas
- Surgery
- Anatomy
- Pathology and Forensic Medicine