脑室内三角区多形性黄色星形细胞瘤:一种罕见且预后良好的年轻成人病例报告。

Asian journal of neurosurgery Pub Date : 2025-05-01 eCollection Date: 2025-09-01 DOI:10.1055/s-0045-1809031
Chonnawee Chaisawasthomrong
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引用次数: 0

摘要

多形性黄色星形细胞瘤(PXA)是一种罕见的II级星形细胞瘤,通常发生在颞叶,通常表现为癫痫发作。我们报告一个独特的病例脑室三角区PXA,一个罕见的位置,模仿脑室脑膜瘤的成像。一位26岁的男性患者表现为进行性视力丧失,磁共振成像显示右侧侧脑室有明显病变。患者行肿瘤次全切除,辅助放疗。组织病理学分析证实PXA伴BRAF V600E突变,随后影像学显示肿瘤控制成功,2年后无复发。该病例强调了将PXA与其他肿瘤(如脑膜瘤)区分开来的重要性,并证明了适当治疗后PXA的预后良好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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