Ng'ang'a Njoki, Ratzersdorfer Jonathan, Abdelhak Yaakov
Department of Obstetrics & Gynecology, Hackensack University Medical Center, Hackensack, New Jersey, USA.
Maternal Resources, Hackensack, New Jersey, USA.
BMJ Case Rep. 2017 Jun 5;2017:bcr-2016-219149. doi: 10.1136/bcr-2016-219149.
Uterus didelphys is a congenital abnormality characterised by double uteri, double cervices and a double or single vagina that affects 0.3% to 11% of the general female population. A 23-year-old woman, gravida 3 para 3003, with uterus didelphys, acquired an iatrogenic interuterine septal defect during an otherwise routine primary caesarean delivery for fetal malpresentation. The defect was repaired but noted to have dehisced during her second pregnancy. A repeat caesarean section was performed due to fetal malpresentation after an unsuccessful external cephalic version. The dehisced defect was left unrepaired. During her third pregnancy, the placenta implanted in the right uterus, but the fetus migrated to the left uterus at approximately 28 weeks gestation. The umbilical cord traversed the interuterine septal defect. With the fetus in the vertex presentation at term gestation, the patient underwent a vaginal birth after two previous caesarean deliveries without any major perinatal complications.
双子宫是一种先天性异常,其特征为双子宫、双宫颈以及双阴道或单阴道,影响0.3%至11%的普通女性人群。一名23岁、孕3产3003的双子宫女性,在因胎儿胎位异常进行的常规初次剖宫产手术中出现了医源性子宫内间隔缺损。该缺损已修复,但在她第二次怀孕时发现裂开。因外倒转术失败后胎儿胎位异常,进行了再次剖宫产。裂开的缺损未予修复。在她第三次怀孕时,胎盘植入右子宫,但胎儿在妊娠约28周时迁移至左子宫。脐带穿过子宫内间隔缺损。足月妊娠时胎儿为头先露,该患者在之前两次剖宫产术后经阴道分娩,未出现任何重大围产期并发症。