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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
Full text How to cite this article

Language: Spanish
References: 15
Page: 167-174
PDF size: 463.52 Kb.


Key words:

Angiomyofibroblastoma, Vulvar biopsies, Vaginal biopsies, benign soft tissue neoplasm, Differential diagnosis.

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.


REFERENCES

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Ginecol Obstet Mex. 2025;93