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YWHAE-FAM22 型子宫内膜间质肉瘤的临床病理特征:一种组织学上分级较高且临床表现侵袭性强的肿瘤。

The clinicopathologic features of YWHAE-FAM22 endometrial stromal sarcomas: a histologically high-grade and clinically aggressive tumor.

机构信息

Department of Pathology, Brigham and Women's Hospital, Boston, MA, USA.

出版信息

Am J Surg Pathol. 2012 May;36(5):641-53. doi: 10.1097/PAS.0b013e31824a7b1a.

Abstract

Endometrial stromal sarcoma (ESS) is a genetically heterogenous group of uterine sarcomas, of which almost half are associated with JAZF1 rearrangement. We recently identified a novel genetic fusion between YWHAE and FAM22A/B in ESS harboring t(10;17)(q22;p13) and herein describe the clinicopathologic features of 13 YWHAE-FAM22 ESS cases (11 primary and 3 metastatic) and compare them with 20 ESS cases with JAZF1 rearrangement. Ten of 11 primary uterine tumors contained morphologically high-grade areas composed of round cells arranged in nests with a delicate stromal capillary network. The tumor cells showed large nuclei with irregular nuclear contours and significant mitotic activity (>10 mitoses/10 HPF) in addition to focal tumor necrosis, in contrast to JAZF1 ESS, which lacked a nested growth pattern, were composed of cells with small round/oval nuclei, and typically had <5 MF/10 HPF. In 7 of the 11 uterine tumors, there was an additional cytologically bland and mitotically weakly active spindle cell component with a fibrous/fibromyxoid stroma (ESS, fibromyxoid variant). Two metastatic tumors (pulmonary) also contained round cell and spindle cell components, whereas 1 metastasis (vaginal) was composed solely of the spindle cell component. In both primary and metastatic tumors, the spindle cells were diffusely positive for estrogen and progesterone receptors and CD10, in contrast to the round cell areas, which were negative. Clinically, 10 of 12 patients with YWHAE-FAM22 ESS presented with FIGO stages II to III disease, in contrast to only 4 of 16 patients with JAZF1 ESS presenting with stages II to III disease (P<0.05). Tumors with YWHAE-FAM22 rearrangements constitute a distinct group of ESS, which is associated with high-grade morphology and aggressive clinical behavior compared to JAZF1 ESS. Thus, their distinction from typical JAZF1 ESS is important for prognostic and therapeutic purposes.

摘要

子宫内膜间质肉瘤(ESS)是一组遗传异质性的子宫肉瘤,其中近一半与 JAZF1 重排有关。我们最近在携带 t(10;17)(q22;p13)的 ESS 中发现了一种新的 YWHAE 和 FAM22A/B 基因融合,并在此描述了 13 例 YWHAE-FAM22 ESS 病例(11 例原发性和 3 例转移性)的临床病理特征,并将其与 20 例具有 JAZF1 重排的 ESS 病例进行了比较。11 例原发性子宫肿瘤中有 10 例包含形态学上的高级别区域,由排列在精细的间质毛细血管网络中的圆形细胞巢组成。肿瘤细胞表现出大的细胞核,核轮廓不规则,有明显的有丝分裂活性(>10 个有丝分裂/10 HPF),除了局灶性肿瘤坏死,与 JAZF1 ESS 不同,后者缺乏巢状生长模式,由具有小圆/卵圆形核的细胞组成,通常<5 MF/10 HPF。在 11 例子宫肿瘤中有 7 例还存在另外一种细胞学上温和和有丝分裂活性较弱的梭形细胞成分,伴有纤维/纤维粘液样基质(ESS,纤维粘液样变异型)。2 例转移瘤(肺部)也包含圆形细胞和梭形细胞成分,而 1 例转移瘤(阴道)仅由梭形细胞成分组成。在原发和转移肿瘤中,梭形细胞弥漫性表达雌激素和孕激素受体以及 CD10,而与圆形细胞区域相反,后者呈阴性。临床上,12 例 YWHAE-FAM22 ESS 患者中有 10 例表现为 FIGO 分期 II 至 III 期疾病,而 16 例 JAZF1 ESS 患者中仅有 4 例表现为 II 至 III 期疾病(P<0.05)。与 JAZF1 ESS 相比,具有 YWHAE-FAM22 重排的肿瘤构成了 ESS 的一个独特群体,其具有高级别形态和侵袭性临床行为。因此,区分它们与典型的 JAZF1 ESS 对于预后和治疗目的很重要。

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