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Spontaneous dichorionic-diamniotic twins in a noncommunicating uterine horn: A case report

BACKGROUND: We present a rare case of a dichorionic-diamniotic twin pregnancy in a noncommunicating rudimentary uterine horn diagnosed prior to rupture at 12 weeks of gestation. CASE: A 33-year-old woman with history of two prior spontaneous abortions presented with a spontaneously conceived dichori...

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Autores principales: Ross, Megan E., Scott, Stephen, Behbakht, Kian, Harper, Teresa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005551/
https://www.ncbi.nlm.nih.gov/pubmed/32055454
http://dx.doi.org/10.1016/j.crwh.2020.e00177
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author Ross, Megan E.
Scott, Stephen
Behbakht, Kian
Harper, Teresa
author_facet Ross, Megan E.
Scott, Stephen
Behbakht, Kian
Harper, Teresa
author_sort Ross, Megan E.
collection PubMed
description BACKGROUND: We present a rare case of a dichorionic-diamniotic twin pregnancy in a noncommunicating rudimentary uterine horn diagnosed prior to rupture at 12 weeks of gestation. CASE: A 33-year-old woman with history of two prior spontaneous abortions presented with a spontaneously conceived dichorionic-diamniotic twin pregnancy. Routine first-trimester screening ultrasound detected an extrauterine twin pregnancy. The patient was admitted for observation and treatment planning. Magnetic resonance imaging (MRI) of the pelvis led to the radiologic diagnosis of suspected abdominal ectopic pregnancy. Exploratory laparotomy led to an intraoperative diagnosis of twin pregnancy within a rudimentary uterine horn, which was removed without incident. CONCLUSION: This is a rare case of a twin pregnancy contained in a noncommunicating rudimentary uterine horn. The presence of this horn was not detected on ultrasonography or MRI.
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spelling pubmed-70055512020-02-13 Spontaneous dichorionic-diamniotic twins in a noncommunicating uterine horn: A case report Ross, Megan E. Scott, Stephen Behbakht, Kian Harper, Teresa Case Rep Womens Health Article BACKGROUND: We present a rare case of a dichorionic-diamniotic twin pregnancy in a noncommunicating rudimentary uterine horn diagnosed prior to rupture at 12 weeks of gestation. CASE: A 33-year-old woman with history of two prior spontaneous abortions presented with a spontaneously conceived dichorionic-diamniotic twin pregnancy. Routine first-trimester screening ultrasound detected an extrauterine twin pregnancy. The patient was admitted for observation and treatment planning. Magnetic resonance imaging (MRI) of the pelvis led to the radiologic diagnosis of suspected abdominal ectopic pregnancy. Exploratory laparotomy led to an intraoperative diagnosis of twin pregnancy within a rudimentary uterine horn, which was removed without incident. CONCLUSION: This is a rare case of a twin pregnancy contained in a noncommunicating rudimentary uterine horn. The presence of this horn was not detected on ultrasonography or MRI. Elsevier 2020-01-30 /pmc/articles/PMC7005551/ /pubmed/32055454 http://dx.doi.org/10.1016/j.crwh.2020.e00177 Text en © 2020 Published by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Ross, Megan E.
Scott, Stephen
Behbakht, Kian
Harper, Teresa
Spontaneous dichorionic-diamniotic twins in a noncommunicating uterine horn: A case report
title Spontaneous dichorionic-diamniotic twins in a noncommunicating uterine horn: A case report
title_full Spontaneous dichorionic-diamniotic twins in a noncommunicating uterine horn: A case report
title_fullStr Spontaneous dichorionic-diamniotic twins in a noncommunicating uterine horn: A case report
title_full_unstemmed Spontaneous dichorionic-diamniotic twins in a noncommunicating uterine horn: A case report
title_short Spontaneous dichorionic-diamniotic twins in a noncommunicating uterine horn: A case report
title_sort spontaneous dichorionic-diamniotic twins in a noncommunicating uterine horn: a case report
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005551/
https://www.ncbi.nlm.nih.gov/pubmed/32055454
http://dx.doi.org/10.1016/j.crwh.2020.e00177
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