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Multifocal complex glioneuronal tumor in an elderly man: an autopsy study: case report
Jian-Qiang Lu1, Bernd W Scheithauer, Pranshu Sharma
1Department of Pathology, Foothills Medical Centre, University of Calgary, Calgary, Alberta, Canada.
Neurosurgery
|June 3, 2009
Summary
This autopsy case report details a complex glioneuronal tumor in an elderly patient, exhibiting features of both dysembryoplastic neuroepithelial tumors (DNT) and rosette-forming glioneuronal tumors (RGNT). The findings offer insights into the relationship between these rare brain tumors.
Area of Science:
- Neuro-oncology
- Neuropathology
- Tumor Histogenesis
Background:
- Dysembryoplastic neuroepithelial tumors (DNT) and rosette-forming glioneuronal tumors (RGNT) represent distinct entities within the spectrum of glioneuronal neoplasms.
- The clinicopathological characterization of these tumors is continually evolving, with increasing recognition of overlapping features.
Observation:
- A 79-year-old male presented with neurological decline attributed to a third ventricular mass causing obstructive hydrocephalus.
- Autopsy revealed a complex glioneuronal tumor with mixed histological features of DNT (floating neurons) and RGNT (synaptophysin-positive rosettes).
- The tumor exhibited pilocytic astrocytoma characteristics with hemorrhage, alongside distinct DNT and RGNT components, predominantly around the third ventricle.
Findings:
- The autopsy confirmed a rare complex glioneuronal tumor in an elderly patient.
- Histopathological analysis demonstrated a unique combination of DNT and RGNT features within the same lesion.
- The tumor's location centered on the third ventricle was a notable characteristic.
Implications:
- This case highlights the potential for mixed glioneuronal tumors to exhibit features of both DNT and RGNT.
- The findings may contribute to understanding the histogenetic origins and potential relationship between DNT, RGNT, and other mixed glioneuronal tumors.
- The advanced age of the patient and the specific tumor distribution offer unique perspectives on these rare brain neoplasms.

