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由DNA甲基化谱定义的多形性黄色星形细胞瘤的MRI特征

MRI features of pleomorphic xanthoastrocytoma defined by DNA methylation profile.

作者信息

Fawaz R, Aboubakr O, El Sissy F N, Mathon B, Oumoussa B M, Barka B, Mandonnet E, Leclercq D, Touat M, Hoang-Xuan K, Adle-Biassette H, Bielle F, Nichelli L

机构信息

Department of Neuroradiology, Pitié-Salpêtrière hospital, AP-HP, 75013 Paris, France.

Department of Neurosurgery, Hôpitaux Universitaires La Pitié Salpêtrière - Charles Foix, AP-HP, Sorbonne Université, 75013 Paris, France.

出版信息

Rev Neurol (Paris). 2025 Sep;181(7):615-623. doi: 10.1016/j.neurol.2025.04.009. Epub 2025 Jun 4.

Abstract

INTRODUCTION

Pleomorphic xanthoastrocytomas (PXA) are primary brain tumors challenging to diagnose due to their morphological and molecular overlap with other tumors. While DNA methylation profiling (MP) aids pathological classification, it alone may be inconclusive. Magnetic resonance imaging (MRI), routinely performed for lesion assessment, provides valuable information. Combining histo-molecular features, MP, and MRI is thus beneficial, particularly in cases of diagnostic uncertainty. In this study, we retrospectively analyzed MRI features of methylation-confirmed PXAs (mcPXAs) versus tumors with PXA-like histology using WHO 2021 criteria.

METHODS

We included 29 adult patients with tumors displaying PXA-suggestive histology, completed MP, and preoperative MRI. Tumors were classified into three groups: mcPXA, histological PXA with methylation-confirmed glioblastoma (mcGBM), and other MP-confirmed diagnoses (mcMimic). Clinical and molecular data were recorded.

RESULTS

All tumors were supratentorial with heterogeneous enhancement. The mcGBM group showed significantly more peritumoral edema and hypercellularity than mcPXA (P=0.002 and P=0.023). No significant differences were found in tumor location, cystic components, or hemorrhagic content. The BRAF mutation appeared in 89% of mcPXA, 8% of mcGBM, and 29% of mcMimic cases (P<0.05). Our composite MRI and molecular score for PXA diagnosis achieved an area under the curve of 0.95, with 95% specificity and 77% sensitivity.

CONCLUSION

In cases of histological uncertainty, lack of peritumoral edema and hypercellularity supports a PXA epigenetic profile. Our specific score could aid in challenging cases, though further validation in larger cohorts is warranted.

摘要

引言

多形性黄色星形细胞瘤(PXA)是原发性脑肿瘤,因其在形态学和分子层面与其他肿瘤存在重叠,诊断颇具挑战性。虽然DNA甲基化谱分析(MP)有助于病理分类,但仅凭其可能无法得出结论。用于病变评估的常规磁共振成像(MRI)可提供有价值的信息。因此,将组织分子特征、MP和MRI相结合是有益的,尤其是在诊断存在不确定性的病例中。在本研究中,我们使用世界卫生组织2021年标准,回顾性分析了甲基化确诊的PXA(mcPXA)与具有PXA样组织学特征的肿瘤的MRI特征。

方法

我们纳入了29例组织学表现提示为PXA、完成了MP且术前行MRI检查的成年患者。肿瘤被分为三组:mcPXA、甲基化确诊的胶质母细胞瘤(mcGBM)伴组织学PXA以及其他MP确诊的诊断(mcMimic)。记录临床和分子数据。

结果

所有肿瘤均位于幕上,强化不均匀。mcGBM组的瘤周水肿和细胞增多明显多于mcPXA组(P = 0.002和P = 0.023)。在肿瘤位置、囊性成分或出血含量方面未发现显著差异。BRAF突变出现在89%的mcPXA病例、8%的mcGBM病例和29%的mcMimic病例中(P<0.05)。我们用于PXA诊断的综合MRI和分子评分的曲线下面积为0.95,特异性为95%,敏感性为77%。

结论

在组织学存在不确定性的病例中,缺乏瘤周水肿和细胞增多支持PXA的表观遗传学特征。我们的特定评分有助于诊断疑难病例,不过仍需在更大队列中进行进一步验证。

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