Orozco CRJ, Ramírez SA, Zaragoza TRM

Language: Spanish
References: 3
Page: 173-175
PDF size: 138.33 Kb.

ABSTRACT

Introduction: the Mayer-Rokitansky-Küster-Hauser syndrome is a congenital disorder characterized by vaginal agenesia, variable uterine development, and functional ovaries. There have been described conservative and surgical techniques to create a space that allows penetration. Case report: a 18-year-old woman with primary amenorrhea and vaginal agenesis that desires to initiate an active sexual life. We create a neovagina with McIndoe's technique using a biological porcine graft. Conclusion: the vaginoplasties with xenografts decrease the morbidity associated with autologous grafts.

REFERENCES

1. Fontana L, Gentilin B, Fedele L, Gervasini C, Miozzo M. Genetics of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome. Clin Genet. 2017; 91 (2): 233-246.

2. Herlin MK, Petersen MB, Brannstrom M. Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a comprehensive update. Orphanet J Rare Dis. 2020; 15 (1): 214.

3. Linder BJ, Gebhart JB. McIndoe neovagina creation for the management of vaginal agenesis. Int Urogynecol J. 2021; 32 (2): 453-455.