子宫内膜间质肉瘤
病理
川东北117
免疫组织化学
血液病理学
组织学
异型性
融合基因
医学
核异型性
间质细胞
生物
川地34
细胞遗传学
染色体
基因
生物化学
遗传学
干细胞
作者
Sorsiah Mansor,Chik Hong Kuick,Sheow Lei Lim,Richard Quek,Adele Pek Choo Wong,Soo Kim Lim-Tan,Timothy Yong Kuei Lim,Kenneth Tou En Chang
标识
DOI:10.1097/pgp.0000000000000523
摘要
A 41-yr-old lady with abnormal uterine bleeding underwent total abdominal hysterectomy. Histologic assessment revealed an endometrial stromal sarcoma (ESS) with minimal cytologic atypia and low mitotic count (up to 7/10 high-power fields) with only focal myxoid areas, morphologically corresponding to a low-grade ESS. Immunohistochemical stains showed cyclin D1 and CD10 positivity, and negative staining for CD117 and progesterone receptor. This tumor was clinically aggressive and recurred 6 mo later. The patient died 19 mo following initial diagnosis. Molecular analysis revealed a ZC3H7B (exon 10)-BCOR (exon 7) gene fusion. Subsequent BCOR immunohistochemistry was weakly positive. ESS with ZC3H7B-BCOR gene fusion is classified as a low-grade ESS in some classification schemes, and is also characterized as being typically myxoid. This report supports emerging evidence that ESS with ZC3H7B-BCOR gene fusion may have an aggressive clinical course in spite of its low-grade histology. This report further expands the morphologic spectrum of ZC3H7B-BCOR fusion ESS to include nonmyxoid histology. Finally, this report underlines the value of molecular analysis in the proper classification of this aggressive tumor with deceptive low-grade histology.
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