Uterine Sarcomas With KDM2B Fusion: Clinicopathological Analysis of Three Cases Supporting a Novel BCOR-Altered Entity

Pavel Dundr,Jan Novotný,Ben Davidson,Francesca Micci,Marcin Jedryka,Tymoteus Poprawski,Michaela Kendall Bártů,Jitka Hausnerová,Michaela Koblížková,Radoslav Matěj,Kristýna Němejcová,Jan Hojný,Nikola Kudrnová
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Abstract

High-grade endometrial stromal sarcomas (HGESS) with BCOR-alteration include sarcomas with YWHAE::NUTM2A/B fusion, ZC3H7B::BCOR fusion, BCOR -ITD, BCOR alternative fusion, and BCORL1 fusion. Recently, 4 cases of uterine sarcomas with KDM2B fusion have been described, which were suggested to belong to the category of BCOR-altered tumors. These tumors are characterized by recurrent fusions of the KDM2B gene with fusion partners including EPC1 , EP400 , and CITED1 . Morphologically, some of them may have a nonspecific spindle-cell or round-cell appearance. In other tumors, however, peculiar morphologic features combining atypical round cells with at least focal sex cord-like features and myxoid stroma were found. In our study, we described 3 additional cases of uterine sarcomas with KDM2B fusion, with fusion partners including EPC1 , EPC2 , and CREBBP . Morphologically, these tumors showed either pure spindle-cell morphology, a combination of spindle and round cells, or a heterogeneous pattern with spindle cells, round cells, and prominent hyalinization, with only focal, vague sex cord-like features. Despite possible morphologic overlap with low-grade endometrial stromal sarcomas in some cases, these tumors seem to represent a variant of HGESS belonging to the category of BCOR-altered sarcomas and have a propensity for aggressive behavior, as 2 of our patients died of disease, and the third had pelvic recurrence before being lost to follow-up.
KDM2B融合的子宫肉瘤:三例支持新型bcr改变实体的临床病理分析
BCOR改变的高级别子宫内膜间质肉瘤(HGESS)包括YWHAE::NUTM2A/B融合、ZC3H7B::BCOR融合、BCOR -ITD、BCOR替代融合和BCORL1融合的肉瘤。近年来报道了4例KDM2B融合的子宫肉瘤,提示属于bcr改变肿瘤的范畴。这些肿瘤的特征是KDM2B基因与包括EPC1、EP400和CITED1在内的融合伙伴反复融合。在形态学上,它们中的一些可能具有非特异性的梭形细胞或圆细胞外观。然而,在其他肿瘤中,发现了特殊的形态特征,包括不典型的圆形细胞,至少有局灶性索样特征和粘液样基质。在我们的研究中,我们描述了另外3例KDM2B融合的子宫肉瘤,融合伴侣包括EPC1、EPC2和CREBBP。形态学上,这些肿瘤表现为纯粹的纺锤形细胞形态,纺锤形细胞和圆形细胞的结合,或纺锤形细胞、圆形细胞和明显的透明化的异质模式,只有局灶性的、模糊的性索样特征。尽管在某些病例中可能与低级别子宫内膜间质肉瘤在形态上有重叠,但这些肿瘤似乎代表了HGESS的一种变体,属于bcr改变的肉瘤类别,并且具有攻击行为倾向,因为我们的2例患者死于疾病,第三例患者在失去随访之前盆腔复发。
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