Majmudar B, Ghanee N, Horowitz I R, Graham D
Department of Pathology, Emory University School of Medicine, Atlanta, GA 30335, USA.
Arch Pathol Lab Med. 1998 Sep;122(9):842-5.
This case report describes a 31-year-old woman at 8 weeks' gestation with large arteriovenous malformation of the uterus involving bilateral uterine and ovarian arteries. She had a history of multiple pregnancy losses, as well as spontaneous copious vaginal hemorrhage. The patient underwent an embolization procedure followed by total abdominal hysterectomy and bilateral salpingo-oophorectomy. The uterus was very small (30 g) despite its gravid status, and the overall microscopic findings indicated Müllerian system hypoplasia in addition to vascular malformation.
本病例报告描述了一名妊娠8周的31岁女性,患有累及双侧子宫和卵巢动脉的子宫大型动静脉畸形。她有多次妊娠丢失史,以及自发性大量阴道出血。患者接受了栓塞手术,随后进行了全腹子宫切除术和双侧输卵管卵巢切除术。尽管处于妊娠状态,但子宫非常小(30克),总体显微镜检查结果表明除血管畸形外,还有苗勒氏系统发育不全。