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病例报告:在一例类似卵巢性索肿瘤的恶性子宫肿瘤中发现ESR1::CITED2融合基因。

Case Report: ESR1::CITED2 Fusion in a Malignant Uterine Tumor Resembling Ovarian Sex Cord Tumor.

作者信息

Abbasi Ferheen, Nucci Marisa R, Doron Ben, Ruskin Rachel, Chien Jeremy, Watkins Jaclyn C, Karnezis Anthony N

机构信息

School of Medicine, University of California Davis, Sacramento, California.

Department of Pathology, Brigham and Women's Hospital/Harvard Medical School, Boston, Massachusetts.

出版信息

Int J Gynecol Pathol. 2025 Jul 1;44(4):368-373. doi: 10.1097/PGP.0000000000001092. Epub 2025 Jan 9.

Abstract

Uterine tumor resembling ovarian sex cord tumor (UTROSCT) is a rare, typically benign uterine tumor occurring over a wide age range (mean 52.4 yr). UTROSCTs often harbor translocations between ESR1 and nuclear receptor coactivators NCOA1-NCOA3 . Here, we present a 21-yr-old woman with a 16 cm complex uterine mass on CT. Grossly, the tumor had an infiltrative appearance. Histologically, it consisted of mild to moderately atypical, spindled cells with ovoid nuclei, growing in fascicles and cords within fibrous to myxohyaline stroma, with tongue-like infiltration of the myometrium. Immunohistochemically, tumor cells were positive for AE1/AE3, ER, PR, vimentin, WT-1, and CD56, and negative for inhibin, calretinin, SMA, desmin, and CD10. Whole exome and whole transcriptome sequencing identified a pathogenic ESR1::CITED2 fusion. The tumor recurred twice (15 and 21 mo after initial surgery) in the abdomen and pelvis. Taken together, the findings suggest this tumor may represent a malignant UTROSCT variant with a novel translocation.

摘要

子宫肿瘤样卵巢性索肿瘤(UTROSCT)是一种罕见的、通常为良性的子宫肿瘤,发病年龄范围较广(平均52.4岁)。UTROSCT常存在雌激素受体1(ESR1)与核受体共激活因子NCOA1 - NCOA3之间的易位。在此,我们报告一名21岁女性,CT检查发现子宫有一个16厘米的复杂肿块。大体上,肿瘤呈浸润性外观。组织学上,它由轻度至中度非典型的梭形细胞组成,细胞核呈卵圆形,在纤维性至黏液透明样基质中呈束状和条索状生长,并呈舌状浸润子宫肌层。免疫组化显示,肿瘤细胞AE1/AE3、雌激素受体(ER)、孕激素受体(PR)、波形蛋白、威尔姆斯瘤蛋白1(WT - 1)和CD56呈阳性,而抑制素、钙视网膜蛋白、平滑肌肌动蛋白(SMA)、结蛋白和CD10呈阴性。全外显子组和全转录组测序鉴定出一种致病性ESR1::CITED2融合。肿瘤在腹部和盆腔复发两次(初次手术后15个月和21个月)。综合来看,这些发现提示该肿瘤可能代表一种具有新型易位的恶性UTROSCT变异型。

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