Adwan Hussamuddin, Patel Bijendra, Kamel Dia, Glazer Geoffrey
Department of Surgery, St Mary's Hospital, London, UK.
Ann R Coll Surg Engl. 2004 Nov;86(6):W1-3. doi: 10.1308/14787080465.
Aggressive angiomyxoma (AAM) was first reported in 1983 as a distinct, slow growing, benign but locally infiltrative, soft tissue tumour. It usually arises in the pelvic and perineal organs, mostly in women. A 47-year-old woman was found to have a large encapsulated retroperitoneal aggressive angiomyxoma. The mass was completely excised via abdomino-perineal approach, and no recurrence noted on MRI at 19 months' follow-up. The encapsulation of this tumour together with other reported rare presentations, suggest an isolated mesenchymal cell origin. A review of the literature is provided.
侵袭性血管黏液瘤（AAM）于1983年首次被报道，是一种独特的、生长缓慢的、良性但具有局部浸润性的软组织肿瘤。它通常发生于盆腔和会阴部器官，多见于女性。一名47岁女性被发现患有一个巨大的包膜性腹膜后侵袭性血管黏液瘤。通过腹会阴联合入路将肿块完全切除，在19个月的随访中，磁共振成像（MRI）未发现复发。该肿瘤的包膜以及其他报道的罕见表现提示其起源于孤立的间充质细胞。本文提供了文献综述。
