新医学2018，Vol.49Issue(6)：453-456,4.DOI:10.3969/j.issn.0253-9802.2018.06.017
血管肌纤维母细胞瘤两例临床病理分析
Clinicopathological analysis of angiomyofibroblastoma:a report of two cases
汪维佳 1廖志波 2古建雄 1陈健宁 3陈冰 1赖骏威 1邵春奎3
作者信息
- 1. 514700 梅州,中山大学附属第三医院粤东医院病理科
- 2. 514700 梅州,中山大学附属第三医院粤东医院肾内科
- 3. 510630 广州中山大学附属第三医院病理科
- 折叠
摘要
Abstract
Angiomyofibroblastoma (AMF)is a type of rare benign soft tissue tumor. It is likely to misdiagnose AMF with other tumors,which is a challenge in pathological diagnosis. Accurate diagnosis can be made based upon comprehensive understanding of the clinical,histopathological and immunohistochemical characteristics of AMF. Here,we reported two female cases of AMF,aged 40 and 43 years. The tumors were located in the vulva and Douglas pouch. They were clinically manifested with painless masses with clear mar-gins. The tumors were composed of blood vessels and fibroblasts under microscopic examination. Immunohisto-chemical staining revealed that Vimentin,Desmin,ER,PR,CD34,Actin were (+),CD117,S-100 and CK were (-). Two patients underwent surgical resection and did not recur postoperatively.关键词
血管肌纤维母细胞瘤/直肠子宫陷凹/免疫组织化学检查/诊断与鉴别诊断Key words
Angiomyofibroblastoma/Douglas pouch/Immunohistochemistry/Diagnosis and differential diagnosis引用本文复制引用
汪维佳,廖志波,古建雄,陈健宁,陈冰,赖骏威,邵春奎..血管肌纤维母细胞瘤两例临床病理分析[J].新医学,2018,49(6):453-456,4.
