Antonacci Celeste, Abballe Luana, Patrizi Sara, Pedace Lucia, Barresi Sabina, Giovannoni Isabella, Tancredi Chantal, Vinciarelli Flavia, Megaro Giacomina, Carai Andrea, Rossi Sabrina, Locatelli Franco, Mastronuzzi Angela, Miele Evelina
Onco-Hematology, Cell Therapy, Gene Therapies and Hemopoietic Transplant, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Pathology Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Acta Neuropathol Commun. 2025 Mar 8;13(1):52. doi: 10.1186/s40478-025-01960-x.
Pineoblastoma is a rare and aggressive malignancy that often affects pediatric populations. Accurate diagnosis is challenging due to histological overlap with other central nervous system tumors and limited molecular data. DNA methylation profiling and analysis of circulating tumor DNA (derived from both cell dissemination as well as cell-free- cfDNA) in cerebrospinal fluid (CSF) are emerging tools for precise tumor classification, in the field of pediatric central nervous system tumors. Here, we report a challenging case of a 17-year-old refugee girl with a previous diagnosis of a primitive neuroectodermal tumor. Formalin-fixed, paraffin-embedded tissue was not available for histopathological re-evaluation. However, the methylation profiling of low amount of CSF-derived DNA classified the tumor as "pineoblastoma, subtype miRNA processing altered 1, subclass A," enabling patient management. The diagnosis was later confirmed through tissue-based DNA methylation analysis of a secondary lesion, demonstrating that the epigenetic signature faithfully reflected tumor features. This case report highlights the potential of CSF-based DNA methylation profiling as a minimally invasive yet accurate diagnostic tool for pediatric CNS tumors. The concordance between CSF and tissue profiling supports the integration of liquid biopsy into diagnostic workflows, allowing for earlier diagnosis and personalized treatment strategies. However, more studies are needed to demonstrate the reliability of our approach in other CNS malignancies.
松果体母细胞瘤是一种罕见且侵袭性强的恶性肿瘤,常影响儿童群体。由于其组织学特征与其他中枢神经系统肿瘤存在重叠,且分子数据有限,准确诊断颇具挑战。在儿童中枢神经系统肿瘤领域,DNA甲基化谱分析以及对脑脊液(CSF)中循环肿瘤DNA(源自细胞播散以及游离cfDNA)的分析正成为精确肿瘤分类的新兴工具。在此,我们报告一例具有挑战性的病例,一名17岁的难民女孩,此前被诊断为原始神经外胚层肿瘤。福尔马林固定、石蜡包埋组织无法用于组织病理学重新评估。然而,对少量脑脊液来源DNA的甲基化谱分析将该肿瘤分类为“松果体母细胞瘤,miRNA加工改变1亚型,A亚类”,从而实现了对患者的管理。该诊断随后通过对继发病变进行基于组织的DNA甲基化分析得到证实,表明表观遗传特征忠实地反映了肿瘤特征。本病例报告强调了基于脑脊液的DNA甲基化谱分析作为一种微创但准确的儿童中枢神经系统肿瘤诊断工具的潜力。脑脊液分析与组织分析结果的一致性支持将液体活检纳入诊断流程,从而实现更早诊断和个性化治疗策略。然而,需要更多研究来证明我们的方法在其他中枢神经系统恶性肿瘤中的可靠性。