Primary Amenorrhea, Aplastic Uterus, and a Functional Vagina: A Rare Case of Mayer-Rokitansky-Küster-Hauser Syndrome

Background. Müllerian agenesis, also known as Mayer-Rokitansky-Küster-Hauser syndrome (MRKHS), a failure of female urogenital development, typically results in a completely stenotic or rudimentary dimple vagina, both of which are generally nonfunctional in adulthood without mechanical dilation or su...

Full description

Bibliographic Details
Main Authors: Gregory W. Kirschen, Natalie Semenyuk
Format: Article
Language:English
Published: Hindawi Limited 2019-01-01
Series:Case Reports in Obstetrics and Gynecology
Online Access:http://dx.doi.org/10.1155/2019/3409548
id doaj-df660b7b9e194ab28d88615b5e57303c
record_format Article
spelling doaj-df660b7b9e194ab28d88615b5e57303c2020-11-24T21:29:03ZengHindawi LimitedCase Reports in Obstetrics and Gynecology2090-66842090-66922019-01-01201910.1155/2019/34095483409548Primary Amenorrhea, Aplastic Uterus, and a Functional Vagina: A Rare Case of Mayer-Rokitansky-Küster-Hauser SyndromeGregory W. Kirschen0Natalie Semenyuk1Medical Scientist Training Program, Stony Brook Medicine, USAAlbert Einstein College of Medicine, Montefiore Medical Center, USABackground. Müllerian agenesis, also known as Mayer-Rokitansky-Küster-Hauser syndrome (MRKHS), a failure of female urogenital development, typically results in a completely stenotic or rudimentary dimple vagina, both of which are generally nonfunctional in adulthood without mechanical dilation or surgical reconstruction. Case. A 20-year-old Tanner stage V heterosexual woman with normal sexual function since coitarche presented with a chief complaint of primary amenorrhea. She was found to have aplastic uterine buds, absent endometrium/cervix, normal ovaries, and an unusually well-developed lower vagina, a rare presentation of MRKHS. We discuss mechanisms by which the anomaly may have arisen. Summary & Conclusion. This case thus expands the clinical presentation of MRKHS to include a normal appearing vagina with intact sexual function from first sexual encounter, raising interesting questions about the basic underlying embryology.http://dx.doi.org/10.1155/2019/3409548
collection DOAJ
language English
format Article
sources DOAJ
author Gregory W. Kirschen
Natalie Semenyuk
spellingShingle Gregory W. Kirschen
Natalie Semenyuk
Primary Amenorrhea, Aplastic Uterus, and a Functional Vagina: A Rare Case of Mayer-Rokitansky-Küster-Hauser Syndrome
Case Reports in Obstetrics and Gynecology
author_facet Gregory W. Kirschen
Natalie Semenyuk
author_sort Gregory W. Kirschen
title Primary Amenorrhea, Aplastic Uterus, and a Functional Vagina: A Rare Case of Mayer-Rokitansky-Küster-Hauser Syndrome
title_short Primary Amenorrhea, Aplastic Uterus, and a Functional Vagina: A Rare Case of Mayer-Rokitansky-Küster-Hauser Syndrome
title_full Primary Amenorrhea, Aplastic Uterus, and a Functional Vagina: A Rare Case of Mayer-Rokitansky-Küster-Hauser Syndrome
title_fullStr Primary Amenorrhea, Aplastic Uterus, and a Functional Vagina: A Rare Case of Mayer-Rokitansky-Küster-Hauser Syndrome
title_full_unstemmed Primary Amenorrhea, Aplastic Uterus, and a Functional Vagina: A Rare Case of Mayer-Rokitansky-Küster-Hauser Syndrome
title_sort primary amenorrhea, aplastic uterus, and a functional vagina: a rare case of mayer-rokitansky-küster-hauser syndrome
publisher Hindawi Limited
series Case Reports in Obstetrics and Gynecology
issn 2090-6684
2090-6692
publishDate 2019-01-01
description Background. Müllerian agenesis, also known as Mayer-Rokitansky-Küster-Hauser syndrome (MRKHS), a failure of female urogenital development, typically results in a completely stenotic or rudimentary dimple vagina, both of which are generally nonfunctional in adulthood without mechanical dilation or surgical reconstruction. Case. A 20-year-old Tanner stage V heterosexual woman with normal sexual function since coitarche presented with a chief complaint of primary amenorrhea. She was found to have aplastic uterine buds, absent endometrium/cervix, normal ovaries, and an unusually well-developed lower vagina, a rare presentation of MRKHS. We discuss mechanisms by which the anomaly may have arisen. Summary & Conclusion. This case thus expands the clinical presentation of MRKHS to include a normal appearing vagina with intact sexual function from first sexual encounter, raising interesting questions about the basic underlying embryology.
url http://dx.doi.org/10.1155/2019/3409548
work_keys_str_mv AT gregorywkirschen primaryamenorrheaaplasticuterusandafunctionalvaginaararecaseofmayerrokitanskykusterhausersyndrome
AT nataliesemenyuk primaryamenorrheaaplasticuterusandafunctionalvaginaararecaseofmayerrokitanskykusterhausersyndrome
_version_ 1725967745392050176