Volume 10, Issue 1 (Winter 2021)                   aumj 2021, 10(1): 1-5 | Back to browse issues page


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Delshad S, Mardi P. Successful Surgical Treatment for Vaginal Agenesis: Report of Two Cases of Mayer–Rokitansky–Küster–Hauser (MRKH) Syndrome. aumj 2021; 10 (1) :1-5
URL: http://aums.abzums.ac.ir/article-1-1242-en.html
1- , salaheddin.delshad1@gmail.com
2- Student Research Committee, Alborz University of Medical Sciences, Karaj, Iran
Abstract:   (2226 Views)
Introduction: Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome is a rare disorder in women which identified as agenesis of vagina and hypoplasia or agenesis of uterine.
Case presentation: in this study, two female cases (17, and 19 years old) diagnosed with MRKH (first one type 2, and second one type 1) are described. Both patients were presented with amenorrhea, and absence of vagina orifice. One of the patients also had abdominal pain. MRI and sonography revealed agenesis of vagina and hypoplasia of uterine in first patient and agenesis of vagina and uterine in second patient. Both patients underwent creation of neovagina using sigmoid colon.
Conclusion: intestinal vaginoplasty using sigmoid colon could be a suitable choice for replacement of vagina in vaginal agenesis patients.
Full-Text [PDF 234 kb]   (1179 Downloads)    
Type of Study: Research | Subject: Special
Received: 2021/01/29 | Accepted: 2021/01/29 | Published: 2021/01/29

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