Van der Griend M D, Burda P, Ferrier A J
Department of Obstetrics and Gynecology, Royal North Shore Hospital, Sydney, New South Wales, Australia.
Gynecol Oncol. 1994 Sep;54(3):389-92. doi: 10.1006/gyno.1994.1230.
Angiomyofibroblastoma is a rare, myxoid tumor of the vulva. To date only 12 cases have been reported in the world literature. Patients are usually premenopausal and present with a vulval mass initially diagnosed as a Bartholin's cyst. The lesions are well circumscribed and range from 0.5 to 12 cm in size. Microscopically the tumors are characterized by high cellularity, numerous blood vessels, and plump stromal cells. Treatment is by surgical excision. There are currently no published reports of local recurrence or metastatic disease. Angiomyofibroblastoma should be differentiated from other neoplasms of the vulva where radical surgical treatment is indicated. A Case Report of angiomyofibroblastoma of the periclitoral region diagnosed in a postmenopausal woman is presented.
血管肌成纤维细胞瘤是一种罕见的外阴黏液样肿瘤。迄今为止，世界文献中仅报道了12例。患者通常处于绝经前，表现为外阴肿物，最初被诊断为巴氏腺囊肿。病变边界清晰，大小从0.5厘米至12厘米不等。显微镜下，肿瘤的特征是细胞密度高、血管众多以及基质细胞丰满。治疗方法为手术切除。目前尚无局部复发或转移性疾病的报道。血管肌成纤维细胞瘤应与其他需要进行根治性手术治疗的外阴肿瘤相鉴别。本文报告了一例在绝经后妇女中诊断出的阴蒂周围区域血管肌成纤维细胞瘤病例。
