国际生殖健康/计划生育 ›› 2021, Vol. 40 ›› Issue (3): 198-201.doi: 10.12280/gjszjk.20200473

• 病例报告 • 上一篇    下一篇

外阴阴道壁血管肌纤维母细胞瘤二例及文献复习

于晓枫, 郑晓丹, 蔡晓辉()   

  1. 100050 北京,首都医科大学附属北京友谊医院
  • 收稿日期:2020-08-03 出版日期:2021-05-15 发布日期:2021-05-28
  • 通讯作者: 蔡晓辉 E-mail:caixiaohui2010@126.com

Two Cases Report of Angiomyofibroblastoma in the Vaginal Wall and Vulva, with A Mini Review

YU Xiao-feng, ZHENG Xiao-dan, CAI Xiao-hui()   

  1. Beijing Friendship Hospital Affiliated to Capital Medical University, Beijing 100050, China
  • Received:2020-08-03 Published:2021-05-15 Online:2021-05-28
  • Contact: CAI Xiao-hui E-mail:caixiaohui2010@126.com

摘要:

血管肌纤维母细胞瘤(angiomyofibroblastoma,AMF)是一种罕见的良性软组织肿瘤,主要来源于盆腔软组织间叶细胞。好发于女性,临床表现无特异性,影像学检查使用率低且术前难以确诊,需依靠病理学明确诊断。一般以手术治疗为主,预后良好,复发率极低。现报告2例外阴阴道壁血管肌纤维母细胞瘤病例,探讨该病的临床特点、病理及免疫组化特征、诊治方法及预后情况,并回顾相关文献,加深对该病的认识。

关键词: 肿瘤,肌组织, 外阴, 阴道, 免疫组织化学, 病例报告, 血管肌纤维母细胞瘤

Abstract:

Angiomyofibroblastoma (AMF) as a rare benign soft-tissue tumor is mainly caused by the interstitial cells of the pelvic soft tissue. It tends to occur in women, with non-specific clinical manifestations, low rate of imaging examination and difficulty in preoperative diagnosis. The clear diagnosis is dependent on pathology. Generally, surgery is the main treatment with a good prognosis and a very low recurrence rate. In this paper, two cases of angiomyofibroblastoma in the vaginal wall and vulva were reported. With a mini review, the clinical characteristics, pathological and immunohistochemical characteristics, diagnosis, treatment and prognosis of this disease were discussed.

Key words: Neoplasms,muscle tissue, Vulva, Vagina, Immunohistochemistry, Case reports, Angiomyofibro-blastoma