One case of pregnancy and congenital vesicovaginal fistula.
10.3969/j.issn.1672-7347.2011.04.017
- Author:
Fenghua ZHANG
1
;
Lijuan ZHANG
Author Information
1. Department of Obstetrics and Gynecology, Second Xiangya Hospital, Central South University, Changsha 410011, China.
- Publication Type:Case Reports
- MeSH:
Adult;
Female;
Humans;
Pregnancy;
Pregnancy Complications;
diagnosis;
Vesicovaginal Fistula;
congenital;
diagnosis
- From:
Journal of Central South University(Medical Sciences)
2011;36(4):367-1 p folowing 368
- CountryChina
- Language:Chinese
-
Abstract:
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.
