Case Report : Cervical Cellular Angiofibroma

Case Report: Cervical Cellular Angiofibroma. Introduction and importance: Cellular angiofibroma is a rare benign tumor in the distal genitalia that can occur in women and men aged 46 – 54 years. These tumors are often diagnosed as Bartholin cysts, vulvar cysts, myomas, and unspecified complex tumors . Presentation of case: A 51-year-old female patient with complaints of lumps since 4 months ago but enlarged within 1 week that then diagnosed as a cervical tumor. She was already menopause 1 year ago. On inspection, a reddish solid mass came out of the vaginal introitus with some blackish necrotic appearance. Total abdominal hysterectomy and bilateral salpingo-oophorectomy were performed, and the histological examination confirmed it as a non-specific chronic inflammation and atypical complex endometrial gland hyperplasia. Discussion: Cellular angiofibroma can be caused by the influence of estrogen and progesterone hormone receptors and the sudden transformation of the surrounding tissue. The treatment of cellular angiofibroma is a complete excision of the tumor tissue. However, based on the patient preference