子宫内膜间质肉瘤
肉瘤
融合基因
生物
间质细胞
川地34
梭形细胞肉瘤
病理
侵袭性血管黏液瘤
癌症研究
滑膜肉瘤
免疫组织化学
基质
泌尿生殖系统
基因
解剖
医学
细胞生物学
免疫学
骨盆
遗传学
干细胞
作者
Rebecca Fliorent,Syed T. Hoda,George Jour,José G. Mantilla
摘要
ABSTRACT Gene fusions involving JAZF1 are a recurrent event in low grade endometrial stromal sarcoma, and have been more recently described in few instances of endometrial stromal sarcoma‐like tumors in the genitourinary tract of men. In this article, we describe a previously unreported spindle cell sarcoma harboring an in‐frame JAZF1::NUDT5 gene fusion, arising in the chest wall of a 51‐year‐old man. The tumor had unique morphologic features resembling both endometrial stromal sarcoma and endometrial stromal sarcoma‐like tumors, consisting of a mixture of cytologically bland and pleomorphic spindle cells with brisk mitotic activity, within an alternating myxoid and fibrous stroma. It had diffuse immunohistochemical expression of CD10, CD34 and CD56, and variable expression of androgen receptor. To our knowledge, neoplasms with these clinico‐pathologic characteristics and novel gene fusion have not been previously reported in the English language literature.
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