Suppr超能文献

一种针对复杂U4a型子宫畸形的内镜与超声联合检查方法。

A combined endoscopic and ultrasonographic approach to a complex U4a uterine anomaly.

作者信息

Moawad Gaby, Zizolfi Brunella, Borrelli Danilo, D'Angelo Giuseppe, Nardelli Fabiola, Guerra Serena, Di Spiezio Sardo Attilio

机构信息

Department of Obstetrics and Gynecology, The George Washington University, Washington; Center for Endometriosis and Advanced Pelvic Surgery, Washington, DC, USA.

Department of Public Health, University of Naples Federico II, Naples, Italy.

出版信息

Facts Views Vis Obgyn. 2025 Jun 27;17(2):204-207. doi: 10.52054/FVVO.2025.13. Epub 2025 May 27.

Abstract

BACKGROUND

Uterine malformations are congenital anomalies arising from abnormal Müllerian duct development during embryogenesis. These can be linked to vaginal cysts, resulting in complex malformations. One rare form is the unicornuate uterus, where only one duct develops, leading to complications like severe pain due to a rudimentary, non-communicating horn.

OBJECTIVES

To describe a combined approach using ultrasound, hysteroscopy, and robotic-assisted laparoscopy for complex uterine anomalies.

PARTICIPANT

A 30-year-old nulliparous woman with unilateral kidney agenesis and acute pelvic pain referred to our centre.

INTERVENTION

2D ultrasound suggested a complex malformation. 3D ultrasound and magnetic resonance imaging confirmed a U4a uterus. Hysteroscopy revealed a hemicavity with one tubal ostium. Robotic-assisted laparoscopy enabled right salpingectomy and removal of the rudimentary horn while preserving the ovary. Intraoperative ultrasonography guided the drainage of vaginal cysts. As a result, vaginal cysts were drained, and the rudimentary horn was removed with ovarian preservation. The patient was discharged without complications and spontaneously conceived a healthy pregnancy 8 months later.

CONCLUSIONS

Unicornuate uterus with non-communicating horn and renal agenesis is a rare condition. A combined approach using ultrasound, hysteroscopy, and robotic-assisted laparoscopy allows comprehensive evaluation and treatment.

WHAT IS NEW?: This is the first reported case of simultaneous and synergistic use of hysteroscopy and robotic-assisted laparoscopy for complex genital malformations under ultrasonographic guidance.

摘要

背景

子宫畸形是胚胎发育过程中苗勒管异常发育引起的先天性异常。这些畸形可能与阴道囊肿有关,导致复杂的畸形。一种罕见的形式是单角子宫,只有一条管道发育,会导致诸如因残角、不通的子宫角引起的剧烈疼痛等并发症。

目的

描述一种联合使用超声、宫腔镜和机器人辅助腹腔镜检查来处理复杂子宫畸形的方法。

参与者

一名30岁未生育的女性,有单侧肾缺如和急性盆腔疼痛,转诊至我们中心。

干预措施

二维超声提示复杂畸形。三维超声和磁共振成像证实为U4a型子宫。宫腔镜检查发现一个半宫腔和一个输卵管开口。机器人辅助腹腔镜检查实现了右侧输卵管切除术和残角子宫切除,同时保留了卵巢。术中超声引导下对阴道囊肿进行引流。结果,阴道囊肿得以引流,残角子宫被切除且保留了卵巢。患者出院时无并发症,8个月后自然受孕并孕育了一个健康的胎儿。

结论

伴有不通子宫角和肾缺如的单角子宫是一种罕见的情况。联合使用超声、宫腔镜和机器人辅助腹腔镜检查可进行全面评估和治疗。

新进展

这是首例在超声引导下同时且协同使用宫腔镜和机器人辅助腹腔镜检查治疗复杂生殖器畸形的报道病例。

相似文献

2
The presentation and management of complex female genital malformations.复杂女性生殖器官畸形的表现与处理。
Hum Reprod Update. 2016 Jan-Feb;22(1):48-69. doi: 10.1093/humupd/dmv048. Epub 2015 Nov 3.
9
Uterine distension media for outpatient hysteroscopy.门诊宫腔镜用子宫扩张介质。
Cochrane Database Syst Rev. 2021 Nov 26;11(11):CD006604. doi: 10.1002/14651858.CD006604.pub2.

本文引用的文献

3
Gartner's Duct Cyst of the Vagina: A Case Report.加特纳氏阴道管囊肿:一例报告。
JNMA J Nepal Med Assoc. 2020 Jul 31;58(227):505-507. doi: 10.31729/jnma.5009.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验