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偶然发现双子宫且每个宫腔内均有双胎妊娠;一例罕见病例报告。

Incidental finding of didelphys uterus with twin pregnancy in each cavity; A rare case report.

作者信息

Zeleke Animut Fetene, Tsegaye Mesfin Ayalew, Geremew Tsehaynesh Bayih, Dessie Ananya Agumasie, Hailemariam Tseganesh Mekonnen, Delelegn Bethlehem Workneh

机构信息

Dilla University, College of Medicine and Health Sciences, Department of Internal Medicine, Dilla, Ethiopia.

Dilla University, College of Medicine and Health Sciences, Department of Obstetrics and Gynecology, Dilla, Ethiopia.

出版信息

Int J Surg Case Rep. 2025 Feb;127:110943. doi: 10.1016/j.ijscr.2025.110943. Epub 2025 Jan 24.

Abstract

INTRODUCTION AND IMPORTANCE

Uterine didelphys is a Müllerian duct anomaly with two uteri and cervices, with or without a vaginal septum. A di-cavitary twin pregnancy in a uterus didelphys is an infrequent occurrence.

CASE PRESENTATION

A 27-year-old woman, gravida 3, para 2, at a gestational age of 37 weeks and 4 days, presented with pushing-down pain. A primary lower uterine segment cesarean section was performed due to fetal bradycardia, and incidentally, a second gravid uterus was discovered, necessitating another lower uterine segment cesarean section. Post-operative reevaluation revealed a double cervix but no vaginal septum.

CLINICAL DISCUSSION

Uterine didelphys is a rare Müllerian duct anomaly with two uteri and cervices, often leading to complications during pregnancy. This anomaly develops from the failure of the Müllerian ducts to fuse, constituting approximately 5-11 % of all Müllerian duct anomalies. Pregnancies in women with didelphys uterus face increased risks, particularly with twin gestations, which occur at a rate of about 1 in 1,000,000. Management strategies must be individualized, considering factors such as fetal presentation and maternal preferences, with vaginal delivery being an option when possible. Early detection through appropriate imaging techniques is crucial.

CONCLUSION

Routine follow-ups should actively search for any uterine anomalies. The management of such cases requires individualized care tailored to each specific situation.

摘要

引言与重要性

双子宫是一种苗勒管畸形,有两个子宫和宫颈,可伴有或不伴有阴道纵隔。双子宫内双腔双胎妊娠较为罕见。

病例介绍

一名27岁女性,孕3产2,孕37周4天,因下坠感就诊。因胎儿心动过缓行子宫下段剖宫产术,术中意外发现第二个妊娠子宫,遂行另一次子宫下段剖宫产术。术后复查发现双宫颈,但无阴道纵隔。

临床讨论

双子宫是一种罕见的苗勒管畸形,有两个子宫和宫颈,常导致孕期并发症。这种畸形是由于苗勒管未融合所致,约占所有苗勒管畸形的5%-11%。双子宫女性妊娠面临的风险增加,尤其是双胎妊娠,发生率约为百万分之一。管理策略必须个体化,考虑胎儿先露和产妇偏好等因素,尽可能选择阴道分娩。通过适当的影像学技术早期发现至关重要。

结论

常规随访应积极排查子宫异常情况。此类病例的管理需要根据具体情况进行个体化护理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f94/11803255/445305c142b2/gr1.jpg

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