2025, Number 5
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Ginecol Obstet Mex 2025; 93 (5)
Angiomyofibroblastoma. A rare tumor. Clinicopathological study of four cases
Sarabia OR, García TJP, Amezcua RA
Language: Spanish
References: 15
Page: 167-174
PDF size: 463.52 Kb.
ABSTRACT
Objective: To analyze the clinical and histopathologic characteristics and treatment
of patients with angiomyofibroblastoma.
Materials and Methods: Retrospective and descriptive analysis of patients with
a histopathologic diagnosis of angiomyofibroblastoma treated at the General Hospital
of Albacete between 2006 and 2023. Clinical and histopathologic characteristics,
treatment, and follow-up were analyzed.
Results: A total of 1,919 vulvar biopsies and 824 vaginal biopsies were analyzed.
Benign lesions accounted for 67.07%, dysplastic lesions for 19.68%, and malignant
neoplasms for 13.23% of the specimens. Four cases of patients diagnosed with angiomyofibroblastoma
were identified, representing 0.14% of all lesions. The mean age of
the patients was 41 years with a range of 31 to 55 years. Treatment was entirely surgical
and no recurrences were observed.
Conclusions: Angiomyofibroblastoma is a rare benign soft tissue neoplasm. Differential
diagnosis is crucial because its clinical manifestations and histologic features
may resemble other vulvar mesenchymal tumors, but with different biological behavior
and prognosis.
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