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脑室内三角区多形性黄色星形细胞瘤:一例年轻成人的罕见表现及良好预后——病例报告

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

作者信息

Chaisawasthomrong Chonnawee

机构信息

Division of Neurosurgery, Department of Surgery, Ratchaburi Hospital, Ratchaburi, Thailand.

出版信息

Asian J Neurosurg. 2025 May 1;20(3):646-650. doi: 10.1055/s-0045-1809031. eCollection 2025 Sep.

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.

摘要

多形性黄色瘤型星形细胞瘤(PXA)是一种罕见的二级星形细胞肿瘤,通常位于颞叶,常表现为癫痫发作。我们报告了一例独特的脑室内三角区PXA病例,这是一个罕见的部位,在影像学上酷似脑室内脑膜瘤。一名26岁男性出现进行性视力丧失,磁共振成像显示右侧脑室有一个边界清晰的病变。患者接受了肿瘤次全切除,随后进行了辅助放疗。组织病理学分析证实为伴有BRAF V600E突变的PXA,随后的影像学检查显示肿瘤得到成功控制,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,并表明PXA在得到适当治疗时预后良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b21/12370325/35a767c99e49/10-1055-s-0045-1809031-i2520018-1.jpg

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