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Official publication of TMSS Medical College

TMSS Medical College Journal

Peer-reviewed  ·  English  ·  Published twice a year
ISSN 2309-3234 DOI 10.62948 BM&DC approved — 4-D-2016/1478
A Rare Case of Vulvar Angiomyofibroblastoma in a Young Woman
Nitu SA1* , Rahman DA2
1
Sanjida Akter Nitu, Medical Studen, TMSS Medical College, Thengamra,Bogura, Bangladesh
2
Dr. DM Arifur Rahman, Associate Professor, Department of Histopathology, TMSS Medical College, Bogura
Corresponding Author
Sanjida Akter Nitu
Medical Studen, TMSS Medical College, Thengamra,Bogura, Bangladesh
Abstract
Angiomyofibroblastoma(AMFB) is a rare benign mesenchymal tumor that predominantly affects the vulvovaginal region, commonly diagnosed in middle-aged women. Histopathological and immunohistochemical evaluations remain essential for accurate diagnosis. AMFB typically exhibits slow growth and a low recurrence rate after complete surgical excision. We report a case of vulvar AMFB in a 23-year-old woman, highlighting the diagnostic challenges associated with this uncommon tumor.
Keywords
Angiomyofibroblastoma Vulva
Introduction
Angiomyofibroblastoma is a benign mesenchymal tumor that predominantly affects the vulvovaginal region in a woman, particularly those in their reproductive years." It has been reported as a rare tumor, with limited incidence and data available emphasizing its uncommon nature. It frequently develops in the vulva, though it can be found in the perineum and vagina? The first case series of this tumor was published by Fletcher et al. in 1992. Clinically, angiomyofibroblastoma presents as a painless, slow growing mass, which can be mistaken for other benign conditions like Bartholin’s cyst, lipoma, hemangioma, fibroma, leiomyoma.* This case report discusses a 23-year-old woman with pedunculated vulvar lump, surgically excised and diagnosed as AMFB, underscoring the importance of considering AMFB in the differential diagnosis of vulvar masses.
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