Sandwell and West Birmingham Hospitals NHS Trust, West Bromwich, UK.
Ann R Coll Surg Engl. 2021 Feb;103(2):e59-e64. doi: 10.1308/rcsann.2020.7008.
Aggressive angiomyxoma is a rare mesenchymal tumour, primarily arising in the soft tissue of the pelvis and perineum in women of reproductive age. There is a paucity of evidence on optimal management because of the rarity of these tumours, but the consensus has been for surgical excision. We present the case of a 65-year-old woman who was admitted with left-sided buttock pain and initially diagnosed with a perianal abscess. She underwent examination under anaesthesia rectum with surgical excision of the lesion, subsequent histopathological and immunochemical analysis was suggestive of aggressive angiomyxoma. To complement our case report, we also present a literature review focusing on aggressive angiomyxoma in the ischioanal fossa (also known as the ischiorectal fossa) with only eight cases of primary aggressive angiomyxoma involving the ischioanal fossa documented to date. The primary aims of this case report and literature review are to familiarise clinicians with the clinical, histopathological and immunochemical features of these tumours, and to increase appreciation that despite the rarity of aggressive angiomyxoma, it might be considered in the differential diagnosis of ischioanal lesions.
侵袭性血管黏液瘤是一种罕见的间叶组织肿瘤,主要发生在育龄期妇女的骨盆和会阴软组织中。由于这些肿瘤罕见,因此缺乏最佳治疗方法的证据,但共识一直是手术切除。我们报告了一例 65 岁女性,因左侧臀部疼痛入院,最初诊断为肛周脓肿。她接受了全身麻醉下直肠检查,并进行了病变切除术,随后的组织病理学和免疫化学分析提示为侵袭性血管黏液瘤。为了补充我们的病例报告,我们还进行了文献复习,重点关注坐骨直肠窝(也称为坐骨直肠窝)的侵袭性血管黏液瘤,迄今为止仅记录了 8 例原发性侵袭性血管黏液瘤累及坐骨直肠窝。本病例报告和文献复习的主要目的是使临床医生熟悉这些肿瘤的临床、组织病理学和免疫化学特征,并提高认识,尽管侵袭性血管黏液瘤罕见,但在坐骨直肠病变的鉴别诊断中应考虑到它。