Title: Angiomyofibroblastoma of the Broad Ligament: A Case Report and Literature Review
Authors: A.Khattabi ,Z.Benaboud, M.Benhaddou Idrissi ,N. Mamouni',S.Errarhay,C. Bouchikhi', A.Banani'
Volume: 9
Issue: 8
Pages: 1-4
Publication Date: 2025/08/28
Abstract:
: Angiomyofibroblastoma (AMFB) is a rare benign mesenchymal tumor, initially described in the vulvovaginal region of women of reproductive age [1]. Its extragenital location, particularly in the broad ligament, is exceptional and presents a diagnostic challenge due to its nonspecific clinical presentation and radiological similarity to other benign or malignant pelvic tumors [2,3]. We report a case of angiomyofibroblastoma arising in the broad ligament-an unusual location- to discuss the diagnostic, therapeutic, and histopathological features of this entity in lightoftheexistingliterature. This is a clinical case managed in our Department of Obstetrics and Gynecology. A 42-year-old woman presented with chronic pelvic pain. Clinical examination revealed a firm, mobile, right latero-uterine pelvic mass. Pelvic ultrasound and MRI showed a well-defined, hypovascularized mass. The patient underwent laparotomy with complete excision of the mass, which was located in the broad ligament. Histopathological analysis confirmed the diagnosis of benign angiomyofibroblastoma. AMFB of the broad ligament is an extremely rare but benign entity. Its diagnosis relies on histological examination. The prognosis is favorable after complete excision, with no need for adjuvant therapy. Recognizing this rare tumor is essential to avoid overtreatment, especially in cases initially suspected to be malignant.