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Microcystic meningioma. A case report

S S Paik1, S J Jang, Y W Park

  • 1Department of Pathology, College of Medicine, Hanyang University, Seoul, Korea.

Insights

Microcystic meningioma, a rare brain tumor variant, presents with unique cellular structures and fluid-filled spaces. This case report details a typical example found in the falx cerebri, confirming its distinct nature.

Area of Science:

  • Neuropathology
  • Oncology

Background:

  • Meningiomas are tumors arising from the meninges, the membranes surrounding the brain and spinal cord.
  • Microcystic meningioma is a recognized morphological subtype with specific histological features.

Observation:

  • A case of microcystic meningioma occurred in the falx cerebri of a 41-year-old male patient.
  • The tumor exhibited characteristic histological findings, including loose texture, microcysts, and stellate, vacuolated tumor cells with long cytoplasmic processes.
  • Nests of meningothelial whorls were also present.

Findings:

  • Immunohistochemical analysis revealed diffuse positivity for vimentin, epithelial membrane antigen (EMA), and S-100 protein.
  • Ultrastructural examination confirmed the tumor's meningiomatous origin.

Implications:

  • This case reinforces the distinct pathological identity of microcystic meningioma.
  • Understanding its specific characteristics aids in accurate diagnosis and classification of meningiomas.

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