Yokomine Daisaku, Yoshinaga Mitsuhiro, Baba Yasutaka, Matsuo Takashi, Iguro Yoshifumi, Nakajo Masayuki, Douchi Tsutomu
Department of Obstetrics and Gynecology, Kagoshima University, Kagoshima, Japan.
J Obstet Gynaecol Res. 2009 Feb;35(1):183-8. doi: 10.1111/j.1447-0756.2008.00875.x.
Uterine arteriovenous malformation (AVM) is a rare and potentially life-threatening disease. The present report describes a postmenopausal patient with uterine AVM manifesting recurrent, massive genital bleeding. Uterine artery embolization (UAE) was scheduled before hysterectomy, but UAE was unsuccessful due to the dilated, tortuous internal iliac arteries, and extremely rapid arterial blood flow. Hysterectomy appeared to carry a potential risk of massive blood loss due to multiple dilated vessels around the uterine corpus and cervix. Therefore, six arteries feeding the uterus were surgically ligated. At 10 months after the operation there have been no episodes of atypical genital bleeding.
子宫动静脉畸形(AVM)是一种罕见且可能危及生命的疾病。本报告描述了一名绝经后子宫动静脉畸形患者,表现为反复大量生殖器出血。在子宫切除术前计划进行子宫动脉栓塞术(UAE),但由于髂内动脉扩张、迂曲以及动脉血流极快,UAE未成功。由于子宫体和宫颈周围有多处扩张血管,子宫切除术似乎存在大出血的潜在风险。因此,手术结扎了六条为子宫供血的动脉。术后10个月未出现非典型生殖器出血情况。