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

Journal of Neurosurgery
|January 22, 2005
PubMed

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.