Shimizu Misao, Kondoh Eiji, Ueda Masashi, Kakui Kazuyo, Tatsumi Keiji, Konishi Ikuo
Department of Gynecology and Obstetrics, Kyoto University Graduate School of Medicine, Kyoto, Japan.
J Obstet Gynaecol Res. 2011 Dec;37(12):1887-90. doi: 10.1111/j.1447-0756.2011.01674.x. Epub 2011 Oct 14.
We here report a case of a 33-year-old woman who experienced secondary postpartum hemorrhage (PPH) due to uterine artery pseudoaneurysm rupture. She had intrauterine balloon tamponade for unexplained primary PPH after spontaneous vaginal delivery, and subsequent angiography showed no abnormal contrast extravasation. However, profuse vaginal bleeding occurred 22 days postpartum. Color Doppler ultrasonography demonstrated an anechoic mass with turbulent flow in the lower uterine segment, corresponding to uterine artery pseudoaneurysm. She was successfully treated with selective uterine arterial embolization. Decreased levels of von Willebrand factor and factor VIII led to the diagnosis of von Willebrand disease. When it is determined that a patient has unexplained PPH or uterine artery pseudoaneurysm, a high index of suspicion and further investigation for underlying bleeding disorders is warranted.
我们在此报告一例33岁女性,因子宫动脉假性动脉瘤破裂发生继发性产后出血(PPH)。她在自然阴道分娩后因不明原因的原发性PPH接受了宫腔球囊填塞,随后的血管造影显示没有异常造影剂外渗。然而,产后22天出现大量阴道出血。彩色多普勒超声显示子宫下段有一个无回声团块,伴有血流紊乱,符合子宫动脉假性动脉瘤。她通过选择性子宫动脉栓塞术成功治愈。血管性血友病因子和凝血因子VIII水平降低导致血管性血友病的诊断。当确定患者有不明原因的PPH或子宫动脉假性动脉瘤时,应高度怀疑并进一步调查潜在的出血性疾病。