Aggressive angiomyxoma of left buttock.
Autor: | Akram H; Department of Gynecologic Oncology, Beaumont Health, Royal Oak, Michigan, USA hakram@oakland.edu., Tran D; Department of Gynecologic Oncology, Beaumont Health, Royal Oak, Michigan, USA., Rehman R; Department of Gynecologic Oncology, Beaumont Health, Royal Oak, Michigan, USA., Al-Wahab Z; Department of Gynecologic Oncology, Beaumont Health, Royal Oak, Michigan, USA. |
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Jazyk: | angličtina |
Zdroj: | BMJ case reports [BMJ Case Rep] 2021 Jun 30; Vol. 14 (6). Date of Electronic Publication: 2021 Jun 30. |
DOI: | 10.1136/bcr-2021-241550 |
Abstrakt: | Aggressive angiomyxoma (AA) is a rare mesenchymal tumour that is characterised by increased incidence in women compared with men, local invasion to the surrounding tissue and high recurrence rate. A premenopausal woman presented to clinic with pelvic pressure, intermittent tingling in the thigh and pressure emptying the bladder. CT scan, vaginal and gluteal biopsies, and MRI scan were performed to conclude a final diagnosis of AA. The patient underwent complete resection of the mass. The mass tested positive for oestrogen receptor and progesterone receptor. The patient received leuprolide postoperatively to prevent recurrence. AA should be considered as a differential diagnosis for a pelvic and perineal mass. Patients should be warned of high recurrence rate, necessity of surgical removal and long-term hormonal treatment. Competing Interests: Competing interests: None declared. (© BMJ Publishing Group Limited 2021. No commercial re-use. See rights and permissions. Published by BMJ.) |
Databáze: | MEDLINE |
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