摘要
先天性阴道闭锁(congenital atresia of vagina)是由泌尿生殖窦及苗勒管末端发育异常而未形成贯通的阴道所致,发病率较低。阴道完全闭锁也称为Ⅱ型阴道闭锁,多合并宫颈的发育不良,子宫体发育不良或子宫畸形,在临床上更为罕见。本文对2018年10月吉林大学第二医院妇产科收治后又转诊至北京协和医院的1例Ⅱ型阴道闭锁病例进行临床分析并复习相关文献,总结目前国内外诊断、分型和治疗的进展,以期医生能更好地认识这种生殖道畸形,患者得到个体化治疗,实现更佳预后。
The congenital atresia of vagina is caused by abnormal development of the urogenital sinuses and the ends of the Mullerian tubes and does not form a normalvagina, which is less common. Complete vaginal atresia, also known as type Ⅱ vaginal atresia, is associated with dysplasia of the cervix, dysplasia of the uterine body, or uterine deformity, and is more rare clinically. In this paper, one case of type Ⅱ vaginal atresia who was admitted to the Second Hospital of Jilin University and then transferred to Peking Union Medical College Hospital in October 2018 was clinically analyzed, we also reviewed related literature and summarized the progress of the diagnosis, classification and treatment at home and abroad, in the hope of a doctor to better understand the genital tract malformation, patients to receive individualized treatment and achieve a better prognosis.
作者
张国伟
付美琦
姜颖显
郑玉
向梅
ZHANG Guo-wei;FU Mei-qi;JIANG Ying-xian;ZHENG Yu;XIANG Mei(Department of Obstetrics and Gynecology,The Second Hospital of Jilin University,Changchun 130041,China)
出处
《国际妇产科学杂志》
CAS
2021年第3期318-321,I0002,共5页
Journal of International Obstetrics and Gynecology
关键词
阴道闭锁
诊断
分型
治疗
病例报告
Gynatresia
Diagnosis
Classification
Therapy
Case reports
