Papillary meningioma of the jugular foramen: A case report

Ying Yu1, Haiyang Xu1, Yubo Wang1

  • 1Department of Neurosurgery, The First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.

Oncology Letters
|January 21, 2016
PubMed

Insights

This study details a rare Grade III Papillary Meningioma (PM) case in a young adult. Complete surgical resection led to a favorable four-year outcome with no recurrence, highlighting effective management for this aggressive tumor.

Area of Science:

  • Neurosurgery
  • Neuropathology
  • Oncology

Background:

  • Papillary meningioma (PM) is a rare, aggressive intracranial tumor.
  • Management of PM is challenging due to its behavior.
  • Accurate diagnosis and surgical intervention are crucial.

Purpose of the Study:

  • To report a case of a young adult with a Grade III Papillary Meningioma.
  • To illustrate the diagnostic and management pathway for this rare tumor.
  • To present the long-term follow-up results after surgical resection.

Main Methods:

  • Case presentation of a 21-year-old male with neurological symptoms.
  • Diagnostic imaging including CT and MRI to identify the intracranial mass.
  • Surgical resection followed by histopathological analysis for definitive diagnosis (WHO Grade III).

Main Results:

  • A high-density mass was identified in the left jugular foramen area.
  • Complete surgical resection was achieved with no immediate complications.
  • Histopathology confirmed Grade III Papillary Meningioma.
  • Four-year follow-up showed no evidence of tumor recurrence or transformation.

Conclusions:

  • Complete surgical resection is an effective treatment for Grade III Papillary Meningioma.
  • Long-term surveillance is important for patients with this rare tumor.
  • Early diagnosis and intervention can lead to favorable outcomes.

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