A primary intracranial neuroepithelial neoplasm with novel TCF3::BEND2 fusion: a case report.

IF 6.2 2区 医学 Q1 NEUROSCIENCES Acta Neuropathologica Communications Pub Date : 2024-11-11 DOI:10.1186/s40478-024-01884-y
Linmao Zheng, Tao Luo, Jie Xian, Mengxin Zhang, Xiuyi Pan, Xiang Wang, Qiang Yue, Qiao Zhou, Ni Chen
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Abstract

Astroblastoma, MN1-altered, is a rare circumscribed glial neoplasm that is composed of round, cuboidal, orcolumnar cells with astroblastic perivascular pseudorosettes, often associated with MN1::BEND2 and MN1::CXXC5 fusions. Atroblastoma-like gliomas harbouring EWSR1::BEND2 have been reported that they defined an epigenetically distinct subtype of astroblastoma. We report a case of a 19-year-old female with an intracranial neuroepithelial tumor featuring a novel TCF3::BEND2 fusion. This tumor, while classified as EWSR1::BEND2 gliomas based on DNA methylation, did not exhibit the MN1 alteration or typical astroblastoma morphology. The patient, initially diagnosed as ependymoma WHO grade 2 following surgery for an intracranial tumor four years prior, presented with a suspected recurrence. Magnetic resonance imaging identified a mixed solid-cystic lesion in the temporal area of the left lateral ventricle. For the recurrent tumor, the histological examination revealed the tumor cells predominantly exhibited a solid arrangement, with the solid areas primarily consisting of oval and short-spindle cells. In certain regions, loosely arranged short-spindle cells was observed. The tumor exhibited high cellular density, nuclear atypia, and frequent mitoses, but lacked the hallmark features typically associated with astroblastoma. Immunohistochemistry revealed patchy positivity for GFAP and OLIG2, diffuse positivity for EMA, and a high MIB-1 labeling index. Genome-wide DNA methylation profiling confirmed the tumor's classification as EWSR1::BEND2 gliomas with a high-confidence match and revealed focal deletion of chromosome 9q. Targeted next-generation sequencing identified a TCF3::BEND2 fusion, validated by reverse transcription polymerase chain reaction and Sanger sequencing. This case broadens the genetic spectrum of high-grade neuroepithelial tumor and suggests that BEND2 alterations may serve as critical determinants for this EWSR1::BEND2 glioma subgroup within the methylation classifier.

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伴有新型 TCF3::BEND2 融合的原发性颅内神经上皮肿瘤:病例报告。
星形母细胞瘤(MN1-altered)是一种罕见的环形胶质肿瘤,由圆形、立方体或柱状细胞组成,具有星形母细胞周围血管假膜,通常与 MN1::BEND2 和 MN1::CXXC5 融合有关。有报道称,携带 EWSR1::BEND2 的成胶质细胞瘤是星形母细胞瘤的一种表观遗传学独特亚型。我们报告了一例 19 岁女性颅内神经上皮肿瘤病例,该肿瘤具有新型 TCF3::BEND2 融合。该肿瘤虽然根据DNA甲基化被归类为EWSR1::BEND2胶质瘤,但并未表现出MN1改变或典型的星形母细胞瘤形态。该患者四年前曾因颅内肿瘤接受手术治疗,最初被诊断为上皮瘤,WHO 分级为 2 级。磁共振成像检查发现,左侧外脑室颞区有一个实性囊性混合病灶。复发肿瘤的组织学检查显示,肿瘤细胞主要呈实性排列,实性区域主要由卵圆形和短纺锤形细胞组成。在某些区域观察到排列松散的短纺锤形细胞。肿瘤细胞密度高、核不典型、有丝分裂频繁,但缺乏星形母细胞瘤的典型特征。免疫组化显示 GFAP 和 OLIG2 呈斑片状阳性,EMA 呈弥漫阳性,MIB-1 标记指数较高。全基因组DNA甲基化分析证实该肿瘤属于EWSR1::BEND2胶质瘤,匹配可信度高,并发现9q染色体局灶性缺失。靶向新一代测序发现了TCF3::BEND2融合,并通过反转录聚合酶链反应和桑格测序进行了验证。该病例拓宽了高级别神经上皮肿瘤的基因谱,并提示BEND2改变可能是甲基化分类中EWSR1::BEND2胶质瘤亚组的关键决定因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Acta Neuropathologica Communications
Acta Neuropathologica Communications Medicine-Pathology and Forensic Medicine
CiteScore
11.20
自引率
2.80%
发文量
162
审稿时长
8 weeks
期刊介绍: "Acta Neuropathologica Communications (ANC)" is a peer-reviewed journal that specializes in the rapid publication of research articles focused on the mechanisms underlying neurological diseases. The journal emphasizes the use of molecular, cellular, and morphological techniques applied to experimental or human tissues to investigate the pathogenesis of neurological disorders. ANC is committed to a fast-track publication process, aiming to publish accepted manuscripts within two months of submission. This expedited timeline is designed to ensure that the latest findings in neuroscience and pathology are disseminated quickly to the scientific community, fostering rapid advancements in the field of neurology and neuroscience. The journal's focus on cutting-edge research and its swift publication schedule make it a valuable resource for researchers, clinicians, and other professionals interested in the study and treatment of neurological conditions.
期刊最新文献
High detection rate of circulating-tumor DNA from cerebrospinal fluid of children with central nervous system germ cell tumors. Detection of diagnostic somatic copy number alterations from cerebrospinal fluid cell-free DNA in brain tumor patients. Diffuse pediatric high-grade glioma of methylation-based RTK2A and RTK2B subclasses present distinct radiological and histomolecular features including Gliomatosis cerebri phenotype. A primary intracranial neuroepithelial neoplasm with novel TCF3::BEND2 fusion: a case report. Correction: Revisiting gliomatosis cerebri in adult-type diffuse gliomas: a comprehensive imaging, genomic and clinical analysis.
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