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女性生殖道胚胎型横纹肌肉瘤3例报告并文献复习

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摘要 女性生殖道胚胎型横纹肌肉瘤(embryonal rhabdomyo-sarcoma,ERMS)是一类罕见的肿瘤,占生殖道恶性肿瘤的3%~6%,好发于儿童和青少年,成年人较少见[1]。ERMS最常累及阴道,发生于子宫颈者极其罕见[2]。阴道ERMS常见于5岁以下婴幼儿,70%左右的子宫颈ERMS发生在20岁以前[3]。
出处 《中国实用妇科与产科杂志》 CAS CSCD 北大核心 2023年第6期669-672,共4页 Chinese Journal of Practical Gynecology and Obstetrics
基金 北京市自然科学基金面上项目(7222061)。
关键词 生殖道肿瘤 女性 胚胎型横纹肌肉瘤 DICER1基因突变 genital tumor female embryonal rhabdomyosarcoma DICERI gene mutation
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