Literature DB >> 19430941

Angiomyofibroblastoma: a rare vulvar tumor.

Guillaume Ducarme1, Morgane Valentin, Carine Davitian, Michele Felce-Dachez, Dominique Luton.   

Abstract

INTRODUCTION: Angiomyofibroblastoma is a rare, benign mesenchymal tumor that occurs mainly in the vulval region of middle age (35-45 years) women. CASE: We describe a 41-year-old woman, presenting with a 10-cm right vulvar mass and persistent perineal pain lasting 1 month. A surgical excision of the lesion was performed and a large mass with an intact capsule was sent for pathological examination. The results indicated angiomyofibroblastoma.
CONCLUSION: The differential diagnosis between angiomyofibroblastoma (AMF) and aggressive angiomyxoma (AAM) is very important because prognoses are not the same. AMF is a well-circumscribed lesion, with a weak risk of local non-destructive recurrence. AAM is a locally aggressive and infiltrative neoplasm, with a high risk of local aggressive recurrence. Wide excision with a rim of normal tissue is recommended in all cases of vulvar tumors.

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Year:  2009        PMID: 19430941     DOI: 10.1007/s00404-009-1110-4

Source DB:  PubMed          Journal:  Arch Gynecol Obstet        ISSN: 0932-0067            Impact factor:   2.344


  1 in total

1.  Local recurrent vaginal aggressive angiomyxoma misdiagnosed as cellular angiomyofibroblastoma: A case report.

Authors:  Yin-Feng Wang; Hong-Lang Qian; Hang-Mei Jin
Journal:  Exp Ther Med       Date:  2016-02-19       Impact factor: 2.447

  1 in total

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