摘要
先天性无阴道患者大多数为MRKH综合征,无阴道同时子宫缺如,表现原发性无月经或性交困难。本病应与阴道闭锁、雄激素不敏感综合征等鉴别。治疗可取保守顶压的Frank法,但多数手术行阴道成形术。当今,以开腹或腹腔镜行乙状结肠阴道成形术、腹膜阴道成形术或Vechietti阴道成形术等为主流手术。
Congenital absence of the vagina is usually associated with the Mayer-Rokitansky-Kuster-I-Iauser (MRKH) syndrome, which characterized by absence of vagina and uterus. Patients presenting with primary amenorrhea and dyspareunia should be distin- guished from other defects of genital tract development such as vaginal atresia and androgen insensitivity syndrome. Treatment could be surgical (vaginoplasty) and nonsurgical ( Frank's technique). Currently, the most widely used remedies are laparotomy or laparoscopic Vecchietti procedure and vaginoplasty with sigmoid or peritoneum. Keywords:
出处
《中国实用妇科与产科杂志》
CAS
CSCD
北大核心
2009年第12期895-898,共4页
Chinese Journal of Practical Gynecology and Obstetrics
关键词
先天性无阴道
阴道成形术
移植
congenital absenoe of the vagina
vaginoplasty
transplant