ArticleGynecologic oncology reports2018
A persistent mass: A case of aggressive Angiomyxoma of the vulva.
Article in Gynecologic oncology reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed.
- A Rare Clinical Presentation of Congenital Superficial Angiomyxoma: A Case Report.Clinical case reports · 2025Article
- Article
- Aggressive Angiomyxoma of the Vulva: Which Is the Best Management Strategy? Description of a Case Report and Review of Literature of the Last Ten Years.Journal of clinical medicine · 2023Article
- Radio-pathological and Clinical Correlation of Aggressive Angiomyxoma: Experience of a Tertiary Care Cancer Hospital.The Indian journal of radiology & imaging · 2021Article
- Deep (aggressive) angiomyxoma of the vagina misdiagnosed as Gartner cyst: A case report.International journal of surgery case reports · 2021Article
- Rare case of huge vulvar angiomyofibroblastoma in a young female.Gynecologic oncology reports · 2021Article
- Aggressive angiomyxoma persistently misdiagnosed as an obturator hernia managed with resection and hormonal therapy: case report.Journal of surgical case reports · 2020Article
- Aggressive angiomyxoma presenting as an ischiorectal fossa tumour.BMJ case reports · 2020Article
- Aggressive angiomyxoma: giant recurrence successfully treated with wide excision and adjuvant therapy with GnRH analogue.BMJ case reports · 2018Article
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Authors and funding
4 authors.
Funding
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Abstract
We present a case of aggressive angiomyxoma of the vulva. The patient presented with a persistent, enlarging vulvar mass, initially misdiagnosed as a Bartholin gland cyst. The patient underwent wide local excision, which resulted in total resection of the mass. Final pathology was consistent with aggressive angiomyxoma, a rare soft tissue tumor with a predilection for the female pelvis. Though rare, it is important to consider in the differential diagnosis of a pelvic mass, given the locally aggressive nature of this tumor and propensity for recurrence.
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