在分子证实的小脑毛细胞星形细胞瘤患者中出现的脊髓高级别星形细胞瘤,具有皮瘤样特征。

IF 4.1 Q1 CLINICAL NEUROLOGY
Neuro-oncology advances Pub Date : 2026-04-20 eCollection Date: 2026-01-01 DOI:10.1093/noajnl/vdag104
Xiaoci Rong, Nan Chen, Yanghao Hou, Haiping Zhu, Xuetao Li, Jie Shao, Sujuan Zhou, Dongbing Li, Yun Ning, Wenjuan Gan, Xiaohong Yao, Yulun Huang
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引用次数: 0

摘要

毛细胞星形细胞瘤(PA)是一种良性肿瘤,高级别转化的风险较低。高级别星形细胞瘤伴核样特征(HGAP)是最近发现的一种肿瘤实体,可能是由新生或低级别胶质瘤引起的。在此,我们报告一位同时患有第四脑室PA和脊髓肿瘤的患者。甲基化分析将脑肿瘤分类为PA,将脊柱肿瘤分类为HGAP。两种肿瘤具有相同DNA断点的KIAA1549::BRAF融合,证实了共同的克隆起源。脊柱肿瘤还表现出复杂的染色体拷贝数畸变,包括CDKN2A/B的纯合缺失。这些发现表明,其他的分子改变与肿瘤进展有关。据我们所知,这是第一份在同一患者中提供PA和HGAP的全面、配对分子特征的报告,为它们潜在的进化关系提供了见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spinal high-grade astrocytoma with piloid features arising in a patient with molecularly confirmed cerebellar pilocytic astrocytoma.

Pilocytic astrocytoma (PA) is a benign tumor with a low risk of high-grade transformation. High-grade astrocytoma with piloid features (HGAP) is a recently recognized tumor entity that may arise de novo or from low-grade gliomas. Here, we report a patient harboring both a fourth ventricular PA and a spinal cord tumor. Methylation profiling classified the brain tumor as PA and the spinal tumor as HGAP. Both tumors shared a KIAA1549::BRAF fusion with identical DNA breakpoints, confirming a common clonal origin. The spinal tumor also showed complex chromosome copy number aberrations, including homozygous deletion of CDKN2A/B. These findings suggest additional molecular alterations associated with tumor progression within the piloid lineage. To our knowledge, this is the first report providing comprehensive, paired molecular characterization of both PA and HGAP in the same patient, offering insight into their potential evolutionary relationship.

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CiteScore
6.20
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