摘要
先天性子宫阴道缺如(Mayer-Rokitansky-Küster-Hauser,MRKH)综合征的发生可能与多种基因有关,并有家族遗传性及聚集性。该病的主要治疗方法是人工阴道成形术。随着腹腔镜技术和组织工程技术的应用和发展,研究者均尝试着对手术方式进行改进和创新,并对患者进行长期随访以评价各种术式的治疗效果。综述MRKH综合征的病因和主要手术治疗方式及随访评价结果。
The hypothesis of polygenic/multifactorial causes for MRKH syndrome(congenital utero-vaginal aplasia) has been reinforced,as well as familial heredity and aggregation.Vaginoplasty is the main treatment method.With the application and improvement of laparoscopic operation and tissue engineering technique,researchers have been trying to continuously develop and innovate vaginoplasty,then evaluate the effectiveness of different procedure by long-term follow-up.The article below will overview the causes,the main methods of operation of MRKH and their follow-up results.
出处
《国际妇产科学杂志》
CAS
2011年第3期227-230,共4页
Journal of International Obstetrics and Gynecology
关键词
阴道
腹腔镜
组织工程
随访研究
治疗
MRKH综合征
Vagina
Laparoscopes
Tissue engineering
Follow-up studies
Therapy
MRKH syndrome