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Updated: Mar 27, 2026

An Orthotopic Glioblastoma Mouse Model Maintaining Brain Parenchymal Physical Constraints and Suitable for Intravital Two-photon Microscopy
Published on: April 21, 2014
Intraventricular Glioblastomas
Atef Ben Nsir1, Yassine Gdoura2, Quoc-Anh Thai3
1Department of Neurosurgery, Fattouma Bourguiba University Hospital-University of Medicine of Monastir, Monastir, Tunisia.
Intraventricular glioblastoma is a rare brain tumor, often affecting younger patients. Radical surgery offers improved survival, particularly for isocitrate dehydrogenase-mutated tumors, but long-term monitoring is essential.
Area of Science:
- Neuro-oncology
- Neurosurgery
- Pathology
Background:
- Glioblastoma is the most common primary brain tumor.
- Primary intraventricular glioblastomas are exceptionally rare, with only 21 cases previously reported.
- This study investigates a small cohort of intraventricular glioblastoma cases.
Purpose of the Study:
- To identify and characterize cases of intraventricular glioblastoma.
- To analyze clinical presentation, treatment, and outcomes for these rare tumors.
- To assess the role of surgical resection and molecular markers in patient survival.
Main Methods:
- Retrospective analysis of intracranial glioblastomas treated over 10 years.
- Inclusion criteria: histologically proven intraventricular glioblastoma.
- Data collection included patient demographics, tumor location, surgical approach, adjuvant therapy, and survival.
Main Results:
- Eight patients with intraventricular glioblastoma were identified (age 6-74 years, mean 29.6).
- Hydrocephalus was the primary clinical manifestation; tumors were located in the lateral or third ventricles.
- Median survival was 32.1 months; 3 patients survived, all with isocitrate dehydrogenase (IDH)-mutated tumors.
Conclusions:
- Intraventricular glioblastoma is a rare entity that can occur in young patients.
- It should be considered in the differential diagnosis of intraventricular lesions.
- Radical surgical resection, especially for IDH-mutated tumors, may improve survival, necessitating long-term follow-up due to high recurrence rates.
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