Department of Laboratory Medicine and Pathology, University of Alberta and Royal Alexandra Hospital, Edmonton, AB, Canada.
Department of Pathology, Shuang Ho Hospital, Taipei Medical University.
Am J Surg Pathol. 2019 Jul;43(7):928-942. doi: 10.1097/PAS.0000000000001265.
Uterine mesenchymal tumors are genetically heterogenous; those with uniform cytomorphology, best exemplified by endometrial stromal tumors, often contain various fusion genes. Novel fusions involving ESR1 and GREB1, key factors in sex hormone pathways, have been implicated in rare uterine mesenchymal tumors. Particularly, the fusions between 5'-ESR1/GREB1 and 3'-NCOA2/NCOA3 were recently identified in 4 uterine tumors resembling ovarian sex-cord tumor (UTROSCT). By RNA sequencing, pathology review, and FISH screening, we identified 4 uterine sarcomas harboring rearranged GREB1, including GREB1-NCOA2 and the novel GREB1-NR4A3, GREB1-SS18, and GREB1-NCOA1, validated by RT-PCR and/or FISH. They occurred in the myometrium of postmenopausal women and were pathologically similar despite minor differences. Tumor cells were generally uniform and epithelioid, with vesicular nuclei and distinct to prominent nucleoli. Growth patterns included solid sheets, trabeculae/cords, nests, and fascicles. Only 1 tumor showed small foci of definitive sex-cord components featuring well-formed tubules, retiform structures, Leydig-like cells, and lipid-laden cells and exhibiting convincing immunoreactivity to sex-cord markers (calretinin, α-inhibin, and Melan-A). In contrast, all the 4 classic UTROSCT we collected occurred in premenopausal patients, consisted predominantly of unequivocal sex-cord elements, prominently expressed multiple sex-cord markers, and harbored ESR1-NCOA3 fusion. Combined with previously reported cases, GREB1-rearranged tumors involved significantly older women (P=0.001), tended to be larger and more mitotically active, showed more variable and often inconspicuous sex-cord differentiation, and appeared to behave more aggressively than ESR1-rearranged UTROSCT. Therefore, these 2 groups of tumors might deserve separate consideration, despite some overlapping features and the possibility of belonging to the same disease spectrum.
子宫间质肿瘤在遗传学上具有异质性;那些具有均匀的细胞学形态的肿瘤,以子宫内膜间质肿瘤为最佳代表,通常包含各种融合基因。涉及性激素途径关键因素 ESR1 和 GREB1 的新融合已被认为与罕见的子宫间质肿瘤有关。特别是,在 4 例类似于卵巢性索肿瘤(UTROSCT)的子宫肿瘤中,最近发现了 5'-ESR1/GREB1 与 3'-NCOA2/NCOA3 之间的融合。通过 RNA 测序、病理复习和 FISH 筛选,我们鉴定了 4 例含有重排 GREB1 的子宫肉瘤,包括 GREB1-NCOA2 和新的 GREB1-NR4A3、GREB1-SS18 和 GREB1-NCOA1,通过 RT-PCR 和/或 FISH 验证。它们发生在绝经后妇女的子宫肌层,尽管存在微小差异,但病理上相似。肿瘤细胞通常均匀且上皮样,具有泡状核和明显到突出的核仁。生长模式包括实性片、小梁/索、巢和束。只有 1 例肿瘤显示出明确的性索成分的小灶,具有形成良好的小管、网状结构、Leydig 样细胞和富含脂质的细胞,并表现出对性索标志物(钙视网膜蛋白、α-抑制素和 Melan-A)的强烈免疫反应。相比之下,我们收集的所有 4 例经典 UTROSCT 均发生在绝经前患者中,主要由明确的性索成分组成,强烈表达多种性索标志物,并携带 ESR1-NCOA3 融合。结合以前报道的病例,GREB1 重排肿瘤涉及年龄较大的女性(P=0.001),往往更大且有丝分裂活性更高,显示出更多可变且通常不明显的性索分化,并且似乎比 ESR1 重排的 UTROSCT 更具侵袭性。因此,尽管存在一些重叠特征和可能属于同一疾病谱,但这两组肿瘤可能值得单独考虑。