AI Article Synopsis
- Cellular angiofibroma is a rare, benign soft-tissue tumor often seen in middle-aged women, typically in the vulvar area, and can be mistaken for cancer.
- A 49-year-old woman had a painless tumor found in the left ischiorectal fossa during a routine CT scan, initially suggestive of malignancy.
- After surgical excision and analysis, it was confirmed to be a cellular angiofibroma with no complications, emphasizing the importance of a multidisciplinary approach for diagnosing and treating such rare tumors.
Article Abstract
Cellular angiofibroma is a recently described rare benign soft-tissue tumor more commonly presenting in middle-aged women, often mimicking malignancy. The vulva is most common location. Complete local excision is the best curative treatment and usually there is no recurrence after surgery. We describe a 49-year-old woman with a painless tumor in the left ischiorectal fossa. It was a random finding in a routine computed tomography (CT) scan after resection of ear melanoma 3 years previously. Ultrasonography showed a solid mass, and further magnetic resonance imaging (MRI) suggested a rhabdomyosarcoma. Altogether, these findings indicated malignant disease. An uncomplicated simple excision of the tumor was done in the operating theatre. The mass measured 7×5×5 cm and the histopathological examination found that it was a cellular angiofibroma, a benign lesion. There were no postoperative complications. This case report highlights the need for multidisciplinary team management of rare tumors such as cellular angiofibromas.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7905177 | PMC |
| http://dx.doi.org/10.1016/j.crwh.2021.e00295 | DOI Listing |
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