Zhang Fenghua, Zhang Lijuan
Department of Obstetrics and Gynecology, Second Xiangya Hospital, Central South University, Changsha 410011, China.
Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2011 Apr;36(4):367-8, 1 p folowing 368. doi: 10.3969/j.issn.1672-7347.2011.04.017.
To discuss the diagnosis and therapy of congenital vesicovaginal fistula (VVF). We reported 1 case of pregnancy and congenital VVF and summarized the pathogenesis and characters. Congenital VVF is extremely rare and characterised by continuous urinary leakage,cyclical hematuria with severe suprapubic pain. It is always associated with other urinary tract abnormalities, urinary tract infection and stone. The pathogenesis is related with genetic, environment, drugs, radiation and incomplete fusion of mullerian. The diagnosis relies on clinical manifestation and radiological examinations.Surgical resection is the key to treatment. Pregnancy and congenital VVF is extremely rare and always misdiagnosised associated with other urinary tract abnormalities. Early diagnosis and making sure the location, size and relationship with other tissues are important. Reasonable preoperative preparation, surgical and postoperative surgical care are the key for treatment.
探讨先天性膀胱阴道瘘(VVF)的诊断与治疗。我们报告了1例妊娠合并先天性VVF病例,并总结了其发病机制和特点。先天性VVF极为罕见,其特征为持续性漏尿、周期性血尿伴严重耻骨上区疼痛。它常与其他泌尿系统异常、泌尿系统感染及结石相关。发病机制与遗传、环境、药物、辐射及苗勒管融合不全有关。诊断依赖临床表现及影像学检查。手术切除是治疗的关键。妊娠合并先天性VVF极为罕见,常因合并其他泌尿系统异常而被误诊。早期诊断并明确其位置、大小及与其他组织的关系很重要。合理的术前准备、手术及术后护理是治疗的关键。