中国医药科学2024，Vol.14Issue(14)：191-194,4.DOI:10.20116/j.issn2095-0616.2024.14.46
先天性双子宫合并子宫内膜异位性疾病1例并文献复习
Congenital double uterus complicated with endometriosis disease:a case report and literature review
张滔 1何丝思 1杨永刚2
作者信息
- 1. 四川省绵阳市中医医院妇产科,四川绵阳 621000
- 2. 四川省宜宾市中医院儿科,四川宜宾 610000
- 折叠
摘要
Abstract
Abnormal uterine development,namely congenital uterine anomaly(CUA),is a congenital abnormality of uterine morphology and function caused by the abnormal development,fusion and/or absorption of bilateral Müllerian duct in female reproductive system during 6-20 weeks of embryo.Most patients have symptoms such as infertility,repeated abortion,premature delivery or abnormal fetal position.Endometriosis disease(ED)includes endometriosis(EMT)and adenomyosis(AM),which often coexist.When endometrial glands and stroma appear outside the uterine body,it is called EMT.When endometrial glands and stroma invade the muscle layer,it is called AM.Double uterus complicated with ED is rare in clinic,which can cause menstrual abnormalities,dysmenorrhea,infertility,etc.A case of congenital double uterine malformation complicated with ED is reviewed and analyzed in this paper,and the relevant literatures are searched to analyze and summarize the common clinical problems related to uterus didelphys and ED.关键词
子宫畸形/双子宫/子宫内膜异位症/子宫腺肌病Key words
Uterine anomaly/Double uterus/Endometriosis/Adenomyosis分类
医药卫生引用本文复制引用
张滔,何丝思,杨永刚..先天性双子宫合并子宫内膜异位性疾病1例并文献复习[J].中国医药科学,2024,14(14):191-194,4.
