| Literature DB >> 27050895 |
Chisa Narayama, Masae Ikeda1, Miwa Yasaka, Yu-suke Sagara, Yasuhira Kan-no, Io Hayashi, Atuya Narita, Satoshi Asai, Toshiki Tajima, Masako Shida, Takeshi Hirasawa, Mikio Mikami.
Abstract
We report a case of vulvar aggressive angiomyxoma (AA) which is a rare, slow growing and benign tumor of mesenchymal origin, but has a high risk of local recurrence. A 49-year-old Japanese female was referred to us with a large mass of the left vulva, measuring 15×9.5×9 centimeters. She underwent surgical excision of the tumor with no evidence of recurrence on a 5-year follow up. In this case, histopathological examination and immunohistochemical staining after excision revealed a diagnosis of vulvar AA with estrogen and progesterone receptors positive. Aggressive angiomyxoma of the vulva needs to be distinguished from benign myxoid tumor with a low risk of local recurrence as well as from malignant neoplasma. The first line treatment of AA is complete surgical excision with tumor free margins, it will reduce the recurrence.Entities:
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Year: 2016 PMID: 27050895
Source DB: PubMed Journal: Tokai J Exp Clin Med ISSN: 0385-0005