Laparoscopic Davydov’s Colpopoiesis for a Case of Mayer-Rokitansky-Kuster-Hauser (MRKH) Syndrome

Congenital absence of vagina and uterus has been eponymously called Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome. The vagina may appear as a dimple with the presence of rudimentary uterine primordia and normal functioning ovaries. Its incidence is 1 in 4500 to 5000 female. Patients present with pr...

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Autores principales: Samantray, Subha R, Mohapatra, Ipsita, Harshini, Nikku
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Obstetrics/Gynecology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8054835/
https://www.ncbi.nlm.nih.gov/pubmed/33884233
http://dx.doi.org/10.7759/cureus.13974
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author Samantray, Subha R
Mohapatra, Ipsita
Harshini, Nikku
author_facet Samantray, Subha R
Mohapatra, Ipsita
Harshini, Nikku
author_sort Samantray, Subha R
collection PubMed
description Congenital absence of vagina and uterus has been eponymously called Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome. The vagina may appear as a dimple with the presence of rudimentary uterine primordia and normal functioning ovaries. Its incidence is 1 in 4500 to 5000 female. Patients present with primary amenorrhea, normal external genitalia, and well-developed secondary sexual characteristics. Davydov’s colpopoiesis is one of the methods of vaginoplasty using the patient’s own peritoneum as a graft to line the neovagina. We present here a case of MRKH Syndrome where a laparoscopic Davydov procedure was chosen for vaginal reconstruction.
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spelling pubmed-80548352021-04-20 Laparoscopic Davydov’s Colpopoiesis for a Case of Mayer-Rokitansky-Kuster-Hauser (MRKH) Syndrome Samantray, Subha R Mohapatra, Ipsita Harshini, Nikku Cureus Obstetrics/Gynecology Congenital absence of vagina and uterus has been eponymously called Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome. The vagina may appear as a dimple with the presence of rudimentary uterine primordia and normal functioning ovaries. Its incidence is 1 in 4500 to 5000 female. Patients present with primary amenorrhea, normal external genitalia, and well-developed secondary sexual characteristics. Davydov’s colpopoiesis is one of the methods of vaginoplasty using the patient’s own peritoneum as a graft to line the neovagina. We present here a case of MRKH Syndrome where a laparoscopic Davydov procedure was chosen for vaginal reconstruction. Cureus 2021-03-18 /pmc/articles/PMC8054835/ /pubmed/33884233 http://dx.doi.org/10.7759/cureus.13974 Text en Copyright © 2021, Samantray et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Obstetrics/Gynecology
Samantray, Subha R
Mohapatra, Ipsita
Harshini, Nikku
Laparoscopic Davydov’s Colpopoiesis for a Case of Mayer-Rokitansky-Kuster-Hauser (MRKH) Syndrome
title Laparoscopic Davydov’s Colpopoiesis for a Case of Mayer-Rokitansky-Kuster-Hauser (MRKH) Syndrome
title_full Laparoscopic Davydov’s Colpopoiesis for a Case of Mayer-Rokitansky-Kuster-Hauser (MRKH) Syndrome
title_fullStr Laparoscopic Davydov’s Colpopoiesis for a Case of Mayer-Rokitansky-Kuster-Hauser (MRKH) Syndrome
title_full_unstemmed Laparoscopic Davydov’s Colpopoiesis for a Case of Mayer-Rokitansky-Kuster-Hauser (MRKH) Syndrome
title_short Laparoscopic Davydov’s Colpopoiesis for a Case of Mayer-Rokitansky-Kuster-Hauser (MRKH) Syndrome
title_sort laparoscopic davydov’s colpopoiesis for a case of mayer-rokitansky-kuster-hauser (mrkh) syndrome
topic Obstetrics/Gynecology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8054835/
https://www.ncbi.nlm.nih.gov/pubmed/33884233
http://dx.doi.org/10.7759/cureus.13974
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