Intraventricular Trigone Pleomorphic Xanthoastrocytoma: A Rare Presentation with Favorable Prognosis in a Young Adult—A Case Report

Pleomorphic xanthoastrocytoma (PXA) is a rare, Grade II astrocytic tumor typically found in the temporal lobe and often presents with seizures. We report a unique case of intraventricular trigone PXA, a rare location that mimicked an intraventricular meningioma on imaging. A 26-year-old male presented with progressive visual loss, and magnetic resonance imaging revealed a well-defined lesion in the right lateral ventricle. The patient underwent subtotal tumor resection, followed by adjuvant radiotherapy. Histopathological analysis confirmed PXA with BRAF V600E mutation, and subsequent imaging showed successful tumor control with no recurrence after 2 years. This case highlights the importance of differentiating PXA from other neoplasms, such as meningiomas, and demonstrates the favorable prognosis of PXA when appropriately managed.

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Publication Details

Journal
Asian Journal of Neurosurgery
Published
2025-05-01
DOI
https://doi.org/10.1055/s-0045-1809031
Primary Topic
Sarcoma Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
0.00

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article

Intraventricular Trigone Pleomorphic Xanthoastrocytoma: A Rare Presentation with Favorable Prognosis in a Young Adult—A Case Report

Chonnawee Chaisawasthomrong
2 links
Asian Journal of Neurosurgery
Sarcoma Diagnosis and Treatment
article

Intraventricular Trigone Pleomorphic Xanthoastrocytoma: A Rare Presentation with Favorable Prognosis in a Young Adult—A Case Report

Chonnawee Chaisawasthomrong
article en

Abstract

Pleomorphic xanthoastrocytoma (PXA) is a rare, Grade II astrocytic tumor typically found in the temporal lobe and often presents with seizures. We report a unique case of intraventricular trigone PXA, a rare location that mimicked an intraventricular meningioma on imaging. A 26-year-old male presented with progressive visual loss, and magnetic resonance imaging revealed a well-defined lesion in the right lateral ventricle. The patient underwent subtotal tumor resection, followed by adjuvant radiotherapy. Histopathological analysis confirmed PXA with BRAF V600E mutation, and subsequent imaging showed successful tumor control with no recurrence after 2 years. This case highlights the importance of differentiating PXA from other neoplasms, such as meningiomas, and demonstrates the favorable prognosis of PXA when appropriately managed.

Asian Journal of NeurosurgeryVol. 20(03)
Ratchaburi Hospital (TH)
King Chulalongkorn Memorial Hospital, Chulalongkorn University, Faculty of Medicine, Chulalongkorn University
Openalex Percentile: Top 86%
Sarcoma Diagnosis and Treatment
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