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罗伯特子宫合并子宫横隔的诊断与治疗:一例病例报告及文献复习

Diagnosis and treatment of Robert's uterus combined with transverse uterine septum: a case report and review of the literature.

作者信息

Chen Mingqian, Yang Xiaoyu, Zhang Bin, Fu Jialiang, Lan Yi, Chi Yugang

机构信息

Department of Obstetrics and Gynecology, Women and Children's Hospital of Chongqing Medical University (Chongqing Health Center for Women and Children), Chongqing, China.

Department of Ultrasound, Women and Children's Hospital of Chongqing Medical University (Chongqing Health Center for Women and Children), Chongqing, China.

出版信息

Front Med (Lausanne). 2024 Aug 2;11:1434957. doi: 10.3389/fmed.2024.1434957. eCollection 2024.

Abstract

BACKGROUND

Robert's uterus combined with transverse uterine septum is a rare uterine malformation. Only one case has been reported to date, and it is challenging to diagnose and treat.

CASE PRESENTATION

Here we report the case of a 19-year-old female had undergone multiple treatments at a previous hospital for primary amenorrhea and periodic lower abdominal pain, with the cause remaining unclear. Ultrasonography and magnetic resonance imaging conducted at our hospital displayed the presence of uterine dysplasia with an incomplete septum. Following a multidisciplinary discussion, a preliminary diagnosis of Robert's uterus combined with transverse uterine septum was made. Following this, laparoscopic exploration and ultrasound-guided hysteroscopic metroplasty were performed. The patient experienced periodic menstruation postoperatively and did not manifest periodic lower abdominal pain.

CONCLUSION

Robert's uterus combined with transverse uterine septum is a very rare uterine malformation, with hysteroscopic metroplasty being the preferred surgical option. Nevertheless, preoperative diagnosis is extremely difficult, and there are also many difficulties in the surgical process. This case outlines the diagnostic and treatment process of a patient with Robert's uterus and transverse uterine septum. It is of great significance to fill the gap in clinical diagnosis and treatment of this special uterine malformation.

摘要

背景

罗伯特子宫合并子宫横隔是一种罕见的子宫畸形。迄今为止仅报道过一例,其诊断和治疗具有挑战性。

病例介绍

在此我们报告一名19岁女性的病例,该患者曾因原发性闭经和周期性下腹痛在之前的医院接受过多次治疗,病因仍不明确。我院进行的超声检查和磁共振成像显示存在子宫发育异常伴不完全纵隔。经过多学科讨论,初步诊断为罗伯特子宫合并子宫横隔。此后,进行了腹腔镜探查和超声引导下宫腔镜子宫成形术。患者术后出现周期性月经,未再表现出周期性下腹痛。

结论

罗伯特子宫合并子宫横隔是一种非常罕见的子宫畸形,宫腔镜子宫成形术是首选的手术方式。然而,术前诊断极其困难,手术过程中也存在诸多困难。本病例概述了一名罗伯特子宫合并子宫横隔患者的诊断和治疗过程。填补这种特殊子宫畸形临床诊断和治疗的空白具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37cc/11327016/32fb6d6dc037/fmed-11-1434957-g001.jpg

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