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Amniocele associated with placental abruption: a case report
Amniocele is a rare condition involving herniation of the amniotic sac through a uterine breach. Our case is of a 29-year-old pregnant woman at 31 weeks of pregnancy who presented to the maternity triage of the Mirebalais Teaching Hospital for abdominal pain and the passage of blood through the vagi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10587749/ https://www.ncbi.nlm.nih.gov/pubmed/37868822 http://dx.doi.org/10.1016/j.xagr.2023.100270 |
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author | Gilles, Bernard Robergeau, Fridjof G.S. Massena, Larry M. Nazaire, Maky-Kenson Millien, Christophe |
author_facet | Gilles, Bernard Robergeau, Fridjof G.S. Massena, Larry M. Nazaire, Maky-Kenson Millien, Christophe |
author_sort | Gilles, Bernard |
collection | PubMed |
description | Amniocele is a rare condition involving herniation of the amniotic sac through a uterine breach. Our case is of a 29-year-old pregnant woman at 31 weeks of pregnancy who presented to the maternity triage of the Mirebalais Teaching Hospital for abdominal pain and the passage of blood through the vagina. After an ultrasonographic evaluation, the diagnosis of amniocele was made. In practice, for a third-trimester, nonlaboring pregnant woman with this symptomatology, the most common diagnoses that come to mind are placenta previa and placental abruption. This case highlights that a diagnosis of silent uterine rupture should also be kept in mind knowing that a uterine rupture is a life-threatening event for both the mother and the fetus, therefore, early diagnosis is very important to improve the maternal-fetal prognosis. |
format | Online Article Text |
id | pubmed-10587749 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-105877492023-10-21 Amniocele associated with placental abruption: a case report Gilles, Bernard Robergeau, Fridjof G.S. Massena, Larry M. Nazaire, Maky-Kenson Millien, Christophe AJOG Glob Rep Case Report Amniocele is a rare condition involving herniation of the amniotic sac through a uterine breach. Our case is of a 29-year-old pregnant woman at 31 weeks of pregnancy who presented to the maternity triage of the Mirebalais Teaching Hospital for abdominal pain and the passage of blood through the vagina. After an ultrasonographic evaluation, the diagnosis of amniocele was made. In practice, for a third-trimester, nonlaboring pregnant woman with this symptomatology, the most common diagnoses that come to mind are placenta previa and placental abruption. This case highlights that a diagnosis of silent uterine rupture should also be kept in mind knowing that a uterine rupture is a life-threatening event for both the mother and the fetus, therefore, early diagnosis is very important to improve the maternal-fetal prognosis. Elsevier 2023-09-24 /pmc/articles/PMC10587749/ /pubmed/37868822 http://dx.doi.org/10.1016/j.xagr.2023.100270 Text en © 2023 The Authors https://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 | Case Report Gilles, Bernard Robergeau, Fridjof G.S. Massena, Larry M. Nazaire, Maky-Kenson Millien, Christophe Amniocele associated with placental abruption: a case report |
title | Amniocele associated with placental abruption: a case report |
title_full | Amniocele associated with placental abruption: a case report |
title_fullStr | Amniocele associated with placental abruption: a case report |
title_full_unstemmed | Amniocele associated with placental abruption: a case report |
title_short | Amniocele associated with placental abruption: a case report |
title_sort | amniocele associated with placental abruption: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10587749/ https://www.ncbi.nlm.nih.gov/pubmed/37868822 http://dx.doi.org/10.1016/j.xagr.2023.100270 |
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