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细胞血管纤维瘤:一种罕见的外阴肿瘤病例报告。

Cellular Angiofibroma: A Rare Vulvar Tumor Case Report.

机构信息

Gynecology and Obstetrics Department, Centro Hospitalar Tondela-Viseu, Viseu, Portugal.

Anatomic Pathology Department, Centro Hospitalar Tondela-Viseu, Viseu, Portugal.

出版信息

Rev Bras Ginecol Obstet. 2020 Jun;42(6):365-368. doi: 10.1055/s-0040-1712485. Epub 2020 Jun 30.

Abstract

Cellular angiofibroma (CA)is a rare benign mesenchymal tumor. In women, it occurs mainly in the vulvovaginal region, with vulvar location in 70% of the cases. Its clinical presentation is nonspecific and similar to several other vulvar tumors of different cellular origins. Thus, its histological and immunohistochemical features allow distinction from other tumors. Cellular angiofibromas have good prognosis, despite some risk of relapse. The authors present the case of a 49-year-old woman with a bulky right vulvar lesion, for which the preoperative diagnosis was a Bartholin cyst, but the histological and immunohistochemical evaluation yielded a CA.

摘要

细胞性血管纤维瘤(CA)是一种罕见的良性间叶性肿瘤。在女性中,主要发生于外阴阴道区域,其中 70%的病例发生于外阴。其临床表现无特异性,与其他几种不同细胞来源的外阴肿瘤相似。因此,其组织学和免疫组织化学特征可与其他肿瘤相区别。细胞性血管纤维瘤预后良好,但有一定的复发风险。作者报告了一例 49 岁女性,右侧大阴唇有一肿块,术前诊断为巴氏腺囊肿,但组织学和免疫组织化学评估结果为 CA。

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