Third ventricular chordoid glioma: case report and review of the literature

Masayuki Nakajima1, Satoshi Nakasu, Naoki Hatsuda

  • 1Department of Neurosurgery, Shiga University of Medical Science, Shiga, Japan

Surgical Neurology
|May 27, 2003
PubMed
Abstract

Insights

Chordoid glioma, a rare brain tumor, was treated with partial surgical removal and stereotactic radiosurgery. This approach showed no tumor regrowth at two years, offering a promising treatment option for this rare entity.

Area of Science:

  • Neuro-oncology
  • Neurosurgery
  • Radiation Oncology

Background:

  • Chordoid glioma of the third ventricle is a rare, novel brain tumor entity.
  • This study presents a case and literature review of this rare tumor.

Observation:

  • A 49-year-old woman presented with headache, memory impairment, and incontinence.
  • MRI revealed a large, well-circumscribed third ventricular tumor.
  • The tumor was partially resected via a trans-lamina terminalis approach, with histologic confirmation of chordoid glioma.

Findings:

  • Residual tumor was treated with stereotactic radiosurgery.
  • No tumor regrowth was observed at the 2-year follow-up.
  • Stereotactic radiosurgery demonstrates promising results for residual chordoid glioma.

Implications:

  • Complete surgical resection of third ventricle chordoid glioma is challenging due to tumor location and associated risks.
  • Conventional radiation therapy has limited efficacy on residual chordoid glioma.
  • Stereotactic radiosurgery, specifically Gamma Knife therapy, offers a potentially effective and less invasive treatment option for residual chordoid glioma, with no reported regrowth in this case.