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Multiple meningiomas.

B Sahu1, P Ranganadham, L T Kishore

  • 1Department of Neurosurgery, Nizam's Institute of Medical Sciences, Hyderabad, India.

The Journal of the Association of Physicians of India
|September 1, 1992
PubMed
Summary
This summary is machine-generated.

True multiple meningiomas are rare, even without neurofibromatosis stigmata. This case report details surgical treatment and reviews existing literature on this uncommon condition.

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Area of Science:

  • Neurosurgery
  • Oncology
  • Neuropathology

Background:

  • Multiple meningiomas, defined by Cushing, represent a rare subset of central nervous system tumors.
  • While often associated with neurofibromatosis, sporadic cases can occur, posing diagnostic and therapeutic challenges.

Observation:

  • A 53-year-old male presented with multiple meningiomas.
  • The patient exhibited no clinical or radiological stigmata suggestive of neurofibromatosis.

Findings:

  • Surgical intervention was performed for the patient's multiple meningiomas.
  • A comprehensive review of the literature on multiple meningiomas was conducted.

Implications:

  • This case contributes to the understanding of sporadic multiple meningiomas.
  • Highlights the importance of surgical management and continued research into the etiology of multiple meningiomas.