Meningioangiomatosis: Clinical, Imaging, and Histopathologic Characteristics

Mina S Makary1, Peter Kobalka2, Pierre Giglio3

  • 1Department of Radiology, Division of Neuroradiology, The Ohio State University Wexner Medical Center, Columbus, Ohio, United States.

Insights

Meningioangiomatosis is a rare central nervous system lesion. Early diagnosis and surgical resection of this benign condition offer a good prognosis.

Area of Science:

  • Neuroscience
  • Neuropathology
  • Neuroradiology

Background:

  • Meningioangiomatosis is a rare, benign central nervous system (CNS) lesion.
  • Its variable radiographic appearance complicates preoperative diagnosis.
  • Understanding this condition is crucial for effective patient management.

Observation:

  • We report a case of meningioangiomatosis in a 17-year-old female presenting with seizures, headache, and dizziness.
  • Imaging revealed a predominantly calcified lesion.
  • The patient underwent near-total surgical resection.

Findings:

  • Meningioangiomatosis presents diagnostic challenges due to its diverse imaging characteristics.
  • Calcification can be a prominent feature in some meningioangiomatosis cases.
  • Surgical intervention is a key treatment modality.

Implications:

  • Accurate preoperative diagnosis of meningioangiomatosis remains difficult.
  • Despite diagnostic challenges, surgical resection is associated with favorable outcomes.
  • Increased awareness of meningioangiomatosis aids in timely and appropriate treatment.

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