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Yeungnam Univ J Med > Volume 24(2 Suppl); 2007 > Article
Yeungnam University Journal of Medicine 2007;24(2 Suppl):S710-718.
DOI: https://doi.org/10.12701/yujm.2007.24.2S.S710    Published online December 31, 2007.
Two Cases of Congenital Vaginal Absence
Sung Chul Park1, Hyun Jin Shin2, Hyo Hyun Kim3, Tae Hyung Lee1, Sung Ho Lee1, Doo Jin Lee1
1Department of Obstetrics and Gynecology, College of Medicine, Yeungnam University, Daegu, Korea
2Institute of Biomedical Engineering, Yeungnam University, Daegu, Korea
3Department of Plastic and Reconstructive Surgery, College of Medicine, Yeungnam University, Daegu, Korea
선천성 질 무발생 환자 2 예
박성철1, 신현진2, 김효헌3, 이태형1, 이승호1, 이두진1
1영남대학교 의과대학 산부인과학교실
2영남대학교 의료공학연구소
3영남대학교 의과대학 성형외과학교실
Correspondence:  Doo Jin Lee, Tel: (053) 620-3435, Fax: (053) 654-0676, 
Email: djlee@med.yu.ac.kr
Abstract
Congenital absence of vagina(Mayer-Rokitansky-Küster-Hauser syndrome) is found between 1 in 4,000 and 20,000 female births, and is frequently associated with various urinary tract and skeletal anomalies. As the patients have normal ovarian functions, they appear as normal female phenotype and have normal female karyotype 46, XX. Inability of coitus is one of the main problems they have, so the goal of treatment is to create a vagina adequate to allow sexual activity. Both surgical and nonsurgical approaches have been utilized. The authors experienced two cases of congenital absence of vagina successfully treated by surgical and nonsurgical method.
Key Words: Congenital absence of vagina, Ingram method, McIndoe operation


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