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Multiple meningiomas in a patient with Rubinstein-Taybi syndrome. Case report
Marco J T Verstegen1, Pepijn van den Munckhof, Dirk Troost
1Departments of Neurosurgery and Neuropathology, Academic Medical Center, University of Amsterdam, The Netherlands. M.J.Verstegen@amc.uva.nl
Abstract:
The authors report a case of multiple meningiomas in a 37-year-old woman with Rubinstein-Taybi syndrome. The patient harbored a bifrontal ossifying meningioma and multiple intracranial meningiomas. She underwent surgery for the frontal ossifying meningioma and a right frontoparietal meningioma.
Insights
This case study details a 37-year-old woman with Rubinstein-Taybi syndrome who presented with multiple meningiomas, including a bifrontal ossifying meningioma. Surgical intervention was performed for the ossifying and a frontoparietal meningioma.
Area of Science:
- Neuro-oncology
- Genetics
- Neurology
Background:
- Rubinstein-Taybi syndrome (RTS) is a rare genetic disorder associated with an increased risk of developing tumors.
- Meningiomas are tumors arising from the meninges, the membranes surrounding the brain and spinal cord.
Observation:
- A 37-year-old female patient with diagnosed Rubinstein-Taybi syndrome presented with multiple intracranial meningiomas.
- The patient exhibited a bifrontal ossifying meningioma and additional meningiomas within the cranium.
Findings:
- The case highlights a rare co-occurrence of multiple meningiomas in a patient with Rubinstein-Taybi syndrome.
- Surgical resection was successfully performed for the bifrontal ossifying meningioma and a right frontoparietal meningioma.
Implications:
- This case contributes to understanding the potential oncogenic pathways in Rubinstein-Taybi syndrome.
- Further research may elucidate the specific mechanisms linking RTS to meningioma development.
- Highlights the importance of vigilant neuro-oncological surveillance in patients with RTS.
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