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A young girl with right ovarian torsion and left ovarian ectopy

BACKGROUND: Mayer-Rokitansky-Küster-Hauser (MRKHS) syndrome refers to congenital hypoplasia/aplasia of the uterus, the cervix and the upper 2/3 of the vagina, in females with normal ovaries and fallopian tubes, secondary sexual characteristics and 46 XX karyotype. This condition originates from abno...

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Autores principales: Morabito, Giuliana, Daidone, Alessandro, Murru, Flora, Iaquinto, Marianna, Faleschini, Elena, Barbi, Egidio, Cozzi, Giorgio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7181485/
https://www.ncbi.nlm.nih.gov/pubmed/32326964
http://dx.doi.org/10.1186/s13052-020-0811-y
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author Morabito, Giuliana
Daidone, Alessandro
Murru, Flora
Iaquinto, Marianna
Faleschini, Elena
Barbi, Egidio
Cozzi, Giorgio
author_facet Morabito, Giuliana
Daidone, Alessandro
Murru, Flora
Iaquinto, Marianna
Faleschini, Elena
Barbi, Egidio
Cozzi, Giorgio
author_sort Morabito, Giuliana
collection PubMed
description BACKGROUND: Mayer-Rokitansky-Küster-Hauser (MRKHS) syndrome refers to congenital hypoplasia/aplasia of the uterus, the cervix and the upper 2/3 of the vagina, in females with normal ovaries and fallopian tubes, secondary sexual characteristics and 46 XX karyotype. This condition originates from abnormal development of Müller’s paramesonephric ducts in the early stages of embryonic development. Kidney agenesis or malformations are the most commonly associated with unilateral kidney agenesis. Ovaries may be ectopic in 16–19% of MRKHS patients. Primary amenorrhoea, due to the absence of the uterus, is the most common presentation. Female karyotype confirmation is mandatory to differentiate it from complete androgen insensitivity syndrome and 17-alpha-hydroxylase deficiency. The management of MRKHS is multidisciplinary in order to encompass psychological, medical and surgical issues. CASE PRESENTATION: A four-year-old girl, presented to the emergency department complaining of left groin swelling noted 2 days earlier. The patient had recently been evaluated for an episode of acute abdominal pain and vomiting, with a final diagnosis of right ovarian torsion. At that time, the ultrasound imaging was not able to identify the left kidney, the left ovary and uterus. Surgical abdominal exploration confirmed the right ovarian torsion and was not able to identify the left kidney and the left ovary. Only a remnant of the uterus was present. Therefore, the right ovary was removed, and a diagnosis of MRKHS was made. Ultrasound imaging showed a left inguinal hernia. The hernial sac consisted of a solid oval vascularized formation suggestive of an annexe. The patient underwent a surgical procedure to correct the left inguinal hernia. In the operating setting, the presence of a vascularized, ectopic ovary carrying the tuba inside the hernial sac was observed. CONCLUSIONS: In front of a patient with ovarian torsion and anatomical features suggestive of MRKHS, both the ovaries should always be searched for, with a high suspicion threshold for extrapelvic ovary. Identifying the ectopic ovary, in this case, helped to preserve patient fertility, avoiding a possible torsion.
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spelling pubmed-71814852020-04-28 A young girl with right ovarian torsion and left ovarian ectopy Morabito, Giuliana Daidone, Alessandro Murru, Flora Iaquinto, Marianna Faleschini, Elena Barbi, Egidio Cozzi, Giorgio Ital J Pediatr Case Report BACKGROUND: Mayer-Rokitansky-Küster-Hauser (MRKHS) syndrome refers to congenital hypoplasia/aplasia of the uterus, the cervix and the upper 2/3 of the vagina, in females with normal ovaries and fallopian tubes, secondary sexual characteristics and 46 XX karyotype. This condition originates from abnormal development of Müller’s paramesonephric ducts in the early stages of embryonic development. Kidney agenesis or malformations are the most commonly associated with unilateral kidney agenesis. Ovaries may be ectopic in 16–19% of MRKHS patients. Primary amenorrhoea, due to the absence of the uterus, is the most common presentation. Female karyotype confirmation is mandatory to differentiate it from complete androgen insensitivity syndrome and 17-alpha-hydroxylase deficiency. The management of MRKHS is multidisciplinary in order to encompass psychological, medical and surgical issues. CASE PRESENTATION: A four-year-old girl, presented to the emergency department complaining of left groin swelling noted 2 days earlier. The patient had recently been evaluated for an episode of acute abdominal pain and vomiting, with a final diagnosis of right ovarian torsion. At that time, the ultrasound imaging was not able to identify the left kidney, the left ovary and uterus. Surgical abdominal exploration confirmed the right ovarian torsion and was not able to identify the left kidney and the left ovary. Only a remnant of the uterus was present. Therefore, the right ovary was removed, and a diagnosis of MRKHS was made. Ultrasound imaging showed a left inguinal hernia. The hernial sac consisted of a solid oval vascularized formation suggestive of an annexe. The patient underwent a surgical procedure to correct the left inguinal hernia. In the operating setting, the presence of a vascularized, ectopic ovary carrying the tuba inside the hernial sac was observed. CONCLUSIONS: In front of a patient with ovarian torsion and anatomical features suggestive of MRKHS, both the ovaries should always be searched for, with a high suspicion threshold for extrapelvic ovary. Identifying the ectopic ovary, in this case, helped to preserve patient fertility, avoiding a possible torsion. BioMed Central 2020-04-23 /pmc/articles/PMC7181485/ /pubmed/32326964 http://dx.doi.org/10.1186/s13052-020-0811-y Text en © The Author(s). 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Morabito, Giuliana
Daidone, Alessandro
Murru, Flora
Iaquinto, Marianna
Faleschini, Elena
Barbi, Egidio
Cozzi, Giorgio
A young girl with right ovarian torsion and left ovarian ectopy
title A young girl with right ovarian torsion and left ovarian ectopy
title_full A young girl with right ovarian torsion and left ovarian ectopy
title_fullStr A young girl with right ovarian torsion and left ovarian ectopy
title_full_unstemmed A young girl with right ovarian torsion and left ovarian ectopy
title_short A young girl with right ovarian torsion and left ovarian ectopy
title_sort young girl with right ovarian torsion and left ovarian ectopy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7181485/
https://www.ncbi.nlm.nih.gov/pubmed/32326964
http://dx.doi.org/10.1186/s13052-020-0811-y
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