Krishnan Monica, Parker Victoria Louise, Baxter Andrew J, Jha Swati, Marrappan Banu, Ola Bola
Department of Obstetrics and Gynaecology, Level 4, The Jessop Wing, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, S10 2SF, UK.
Division of Clinical Medicine, Level 4, The Jessop Wing, University of Sheffield, Sheffield, S10 2SF, UK.
Radiol Case Rep. 2024 Sep 26;19(12):6487-6490. doi: 10.1016/j.radcr.2024.08.137. eCollection 2024 Dec.
Rudimentary uterine horn pregnancy is rare, with a reported incidence of 1 in 76,000 to 1 in 150,000. This report aims to advance knowledge regarding this rare condition, importance of MRI imaging in characterizing congenital uterine anomalies and the feasibility of a total laparoscopic management approach. A 26 year old female presented with new onset abdominal pain at 6 weeks gestation. Ultrasound imaging initially suggested that the pregnancy was located within a unicornuate uterus. However further imaging (ultrasound and MRI) instead located the pregnancy within a noncommunicating right-sided rudimentary uterine horn, with a left-sided unicornuate uterus. This uterine anomaly was newly diagnosed in early pregnancy and required a multidisciplinary approach to determine optimal management. A total laparoscopic approach was successfully used to excise the right uterine horn and fallopian tube to prevent recurrence and future complications including tubal ectopic pregnancy.
残角子宫妊娠极为罕见,报告发病率为1/76,000至1/150,000。本报告旨在增进对这种罕见病症的了解,阐述MRI成像在先天性子宫异常特征描述中的重要性以及全腹腔镜管理方法的可行性。一名26岁女性在妊娠6周时出现新发腹痛。超声成像最初提示妊娠位于单角子宫内。然而,进一步的成像检查(超声和MRI)发现妊娠位于右侧非交通性残角子宫内,左侧为单角子宫。这种子宫异常在妊娠早期被新诊断出来,需要多学科方法来确定最佳管理方案。成功采用全腹腔镜方法切除右侧子宫角和输卵管,以防止复发及未来包括输卵管异位妊娠在内的并发症。