Unicornuate Uterus with Rudimentary Horn as a Rare Etiology of Secondary Dysmenorrhea: A Case Report
Congenital uterine anomalies are an uncommon type of female genital malformations caused by abnormal development of müllerian ducts during embryogenesis. Patients with an obstructive uterine anomaly have a higher risk of developing gynecological and obstetric complications that may present at menarc...
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Karger Publishers
2021
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oai:doaj.org-article:8f4ff738f5594517991d27c09f3427622021-12-02T12:40:24ZUnicornuate Uterus with Rudimentary Horn as a Rare Etiology of Secondary Dysmenorrhea: A Case Report2571-726X10.1159/000519872https://doaj.org/article/8f4ff738f5594517991d27c09f3427622021-11-01T00:00:00Zhttps://www.karger.com/Article/FullText/519872https://doaj.org/toc/2571-726XCongenital uterine anomalies are an uncommon type of female genital malformations caused by abnormal development of müllerian ducts during embryogenesis. Patients with an obstructive uterine anomaly have a higher risk of developing gynecological and obstetric complications that may present at menarche or later in life. We present a case of severe dysmenorrhea in a young teenager caused by obstructive hematometra in a noncommunicating horn of the unicornuate uterus. A differential diagnosis of a possible anomaly was made using 2-dimensional pelvic ultrasonography, which was later confirmed using MRI that revealed an anomalous uterine cavity with a single left-sided cornua communicating with the cervix and a distended right-sided rudimentary horn. She underwent a right salpingectomy with rudimentary horn excision, which was successfully managed laparoscopically. This case emphasizes the importance of physicians being cognizant in identifying patients with uterine anomaly to provide appropriate treatment and prevent adverse reproductive outcomes.Zuhdi Khalid NagshabandiBindu IsaacInshia BegumKarger Publishersarticleunicornuate uterusnoncommunicating rudimentary horncongenital uterine anomalymagnetic resonance imagingdysmenorrheaMedicineRENDubai Medical Journal, Pp 1-4 (2021) |
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unicornuate uterus noncommunicating rudimentary horn congenital uterine anomaly magnetic resonance imaging dysmenorrhea Medicine R |
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unicornuate uterus noncommunicating rudimentary horn congenital uterine anomaly magnetic resonance imaging dysmenorrhea Medicine R Zuhdi Khalid Nagshabandi Bindu Isaac Inshia Begum Unicornuate Uterus with Rudimentary Horn as a Rare Etiology of Secondary Dysmenorrhea: A Case Report |
description |
Congenital uterine anomalies are an uncommon type of female genital malformations caused by abnormal development of müllerian ducts during embryogenesis. Patients with an obstructive uterine anomaly have a higher risk of developing gynecological and obstetric complications that may present at menarche or later in life. We present a case of severe dysmenorrhea in a young teenager caused by obstructive hematometra in a noncommunicating horn of the unicornuate uterus. A differential diagnosis of a possible anomaly was made using 2-dimensional pelvic ultrasonography, which was later confirmed using MRI that revealed an anomalous uterine cavity with a single left-sided cornua communicating with the cervix and a distended right-sided rudimentary horn. She underwent a right salpingectomy with rudimentary horn excision, which was successfully managed laparoscopically. This case emphasizes the importance of physicians being cognizant in identifying patients with uterine anomaly to provide appropriate treatment and prevent adverse reproductive outcomes. |
format |
article |
author |
Zuhdi Khalid Nagshabandi Bindu Isaac Inshia Begum |
author_facet |
Zuhdi Khalid Nagshabandi Bindu Isaac Inshia Begum |
author_sort |
Zuhdi Khalid Nagshabandi |
title |
Unicornuate Uterus with Rudimentary Horn as a Rare Etiology of Secondary Dysmenorrhea: A Case Report |
title_short |
Unicornuate Uterus with Rudimentary Horn as a Rare Etiology of Secondary Dysmenorrhea: A Case Report |
title_full |
Unicornuate Uterus with Rudimentary Horn as a Rare Etiology of Secondary Dysmenorrhea: A Case Report |
title_fullStr |
Unicornuate Uterus with Rudimentary Horn as a Rare Etiology of Secondary Dysmenorrhea: A Case Report |
title_full_unstemmed |
Unicornuate Uterus with Rudimentary Horn as a Rare Etiology of Secondary Dysmenorrhea: A Case Report |
title_sort |
unicornuate uterus with rudimentary horn as a rare etiology of secondary dysmenorrhea: a case report |
publisher |
Karger Publishers |
publishDate |
2021 |
url |
https://doaj.org/article/8f4ff738f5594517991d27c09f342762 |
work_keys_str_mv |
AT zuhdikhalidnagshabandi unicornuateuteruswithrudimentaryhornasarareetiologyofsecondarydysmenorrheaacasereport AT binduisaac unicornuateuteruswithrudimentaryhornasarareetiologyofsecondarydysmenorrheaacasereport AT inshiabegum unicornuateuteruswithrudimentaryhornasarareetiologyofsecondarydysmenorrheaacasereport |
_version_ |
1718393751613734912 |