Virginia Tech Carilion School of Medicine, 2 Riverside Circle.
Department of Neurosurgery.
J Pediatr Hematol Oncol. 2024 Jul 1;46(5):e313-e316. doi: 10.1097/MPH.0000000000002885. Epub 2024 Jun 10.
In the most recent fifth edition of the World Health Organization Classification of Tumors of the Central Nervous System, astroblastoma has been defined by molecular rearrangements involving the MN1 gene, with common partners being BEND2 or CXXC5 . Accordingly, this tumor entity is now known as "astroblastoma, MN1 -altered." However, gliomas with EWSR1::BEND2 fusions, devoid of MN1 fusion alterations, have recently been shown to exhibit astroblastoma-like histomorphologic features and reside in a distinct epigenetic subgroup based on DNA methylation studies similar to high-grade neuroepithelial tumor with MN1 alteration, which includes astroblastoma, MN1 altered tumors. This new epigenetically distinct subtype of astroblastoma containing EWSR1::BEND2 fusions lacks the required MN1 alteration and, thus, does not satisfy the current molecular classification of these lesions. Here, we describe a case of glioma with histologic features and DNA methylation profiling consistent with astroblastoma with a novel YAP1: : BEND2 fusion. This case and others further expand the molecular findings observable in astroblastoma-like tumors outside the constraints of MN1 alteration. Such cases of astroblastoma with EWSR1::BEND2 and YAP1::BEND2 fusions challenge the current molecular classification of astroblastoma based solely on an MN1 alteration.
在最近的第五版世界卫生组织中枢神经系统肿瘤分类中,星形母细胞瘤被定义为涉及 MN1 基因的分子重排,常见的伙伴是 BEND2 或 CXXC5。因此,这种肿瘤实体现在被称为“星形母细胞瘤,MN1 改变”。然而,最近已经表明,具有 EWSR1::BEND2 融合但没有 MN1 融合改变的神经胶质瘤表现出类似于星形母细胞瘤的组织形态学特征,并根据 DNA 甲基化研究位于一个独特的表观遗传亚组中,类似于具有 MN1 改变的高级神经上皮肿瘤,其中包括星形母细胞瘤,MN1 改变的肿瘤。这种含有 EWSR1::BEND2 融合的新型表观遗传上不同的星形母细胞瘤亚型缺乏必需的 MN1 改变,因此不符合这些病变的当前分子分类。在这里,我们描述了一例具有组织学特征和 DNA 甲基化谱图的神经胶质瘤,与具有新型 YAP1::BEND2 融合的星形母细胞瘤一致。该病例和其他病例进一步扩展了在 MN1 改变之外的星形母细胞瘤样肿瘤中可观察到的分子发现。具有 EWSR1::BEND2 和 YAP1::BEND2 融合的星形母细胞瘤病例挑战了仅基于 MN1 改变的星形母细胞瘤的当前分子分类。