Grade I meningioma with disseminated bone disease: a rare clinical phenomenon

Oriol Mirallas1, David Marmolejo2, Augusto Valdivia2

  • 1Medical Oncology Department, Vall d'Hebron University Hospital, Barcelona, Spain urimirallas@gmail.com.

BMJ Case Reports
|April 9, 2020
PubMed

Insights

This case report details a rare instance of disseminated grade I meningioma presenting as pelvic bone lesions. It highlights the challenges in treating this rare presentation of a typically benign tumor.

Area of Science:

  • Neuro-oncology
  • Skeletal oncology

Background:

  • Meningioma, the second most common primary central nervous system tumor, is graded I, II, or III.
  • Grade I meningioma, typically benign, rarely disseminates systemically.

Observation:

  • A 48-year-old male with a history of grade I meningioma presented with pelvic pain 3 years post-diagnosis.
  • CT scans revealed new pelvic bone lesions, histopathologically confirmed as grade I meningioma.

Findings:

  • The disseminated grade I meningioma showed resistance to hormonal therapy with octreotide and hydroxyurea.
  • This case represents a rare occurrence of systemic dissemination of a low-grade meningioma.

Implications:

  • Limited data exists on the prevalence and optimal treatment of disseminated meningioma.
  • Sharing clinical experiences, both positive and negative, is crucial for advancing the management of rare meningioma presentations.