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Spontaneous Rupture of an Adrenal Artery in Pregnancy: A Case Report
A spontaneous rupture of an adrenal artery is a rare cause of abdominal pain in pregnancy. We present a case of a pregnant woman who needed to be operated on because of a rupture of the right adrenal artery associated with a fetal bradycardia. An immediate caesarean section was performed. The intra-...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3546435/ https://www.ncbi.nlm.nih.gov/pubmed/23346435 http://dx.doi.org/10.1155/2012/859068 |
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author | Bolla, D. Schyrba, V. Drack, G. Dietler, S. Hornung, R. |
author_facet | Bolla, D. Schyrba, V. Drack, G. Dietler, S. Hornung, R. |
author_sort | Bolla, D. |
collection | PubMed |
description | A spontaneous rupture of an adrenal artery is a rare cause of abdominal pain in pregnancy. We present a case of a pregnant woman who needed to be operated on because of a rupture of the right adrenal artery associated with a fetal bradycardia. An immediate caesarean section was performed. The intra-abdominal palpation identified an extensive retroperitoneal mass near the right kidney and a postoperative computer tomography confirmed an active bleeding near the kidney. For this reason our interventional radiology team, using a right femoral artery approach, performed a flush aortogram and identified the source of bleeding in the right adrenal artery. After two attempts, a coiling of the artery stopped the haemorrhage. The pathogenesis of arterial haemorrhage is still poorly understood although a possible cause could be the excess of hormones during pregnancy, which can lead to a significant arterial wall degeneration. In case of a retroperitoneal bleeding and if the patient is still haemodynamically stable, a transcatheter embolization using microcoils must be considered. This technique is nowadays safe and effective and can be performed within a short time with a lower risk of complications. |
format | Online Article Text |
id | pubmed-3546435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-35464352013-01-23 Spontaneous Rupture of an Adrenal Artery in Pregnancy: A Case Report Bolla, D. Schyrba, V. Drack, G. Dietler, S. Hornung, R. Case Rep Obstet Gynecol Case Report A spontaneous rupture of an adrenal artery is a rare cause of abdominal pain in pregnancy. We present a case of a pregnant woman who needed to be operated on because of a rupture of the right adrenal artery associated with a fetal bradycardia. An immediate caesarean section was performed. The intra-abdominal palpation identified an extensive retroperitoneal mass near the right kidney and a postoperative computer tomography confirmed an active bleeding near the kidney. For this reason our interventional radiology team, using a right femoral artery approach, performed a flush aortogram and identified the source of bleeding in the right adrenal artery. After two attempts, a coiling of the artery stopped the haemorrhage. The pathogenesis of arterial haemorrhage is still poorly understood although a possible cause could be the excess of hormones during pregnancy, which can lead to a significant arterial wall degeneration. In case of a retroperitoneal bleeding and if the patient is still haemodynamically stable, a transcatheter embolization using microcoils must be considered. This technique is nowadays safe and effective and can be performed within a short time with a lower risk of complications. Hindawi Publishing Corporation 2012 2012-12-30 /pmc/articles/PMC3546435/ /pubmed/23346435 http://dx.doi.org/10.1155/2012/859068 Text en Copyright © 2012 D. Bolla et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Bolla, D. Schyrba, V. Drack, G. Dietler, S. Hornung, R. Spontaneous Rupture of an Adrenal Artery in Pregnancy: A Case Report |
title | Spontaneous Rupture of an Adrenal Artery in Pregnancy: A Case Report |
title_full | Spontaneous Rupture of an Adrenal Artery in Pregnancy: A Case Report |
title_fullStr | Spontaneous Rupture of an Adrenal Artery in Pregnancy: A Case Report |
title_full_unstemmed | Spontaneous Rupture of an Adrenal Artery in Pregnancy: A Case Report |
title_short | Spontaneous Rupture of an Adrenal Artery in Pregnancy: A Case Report |
title_sort | spontaneous rupture of an adrenal artery in pregnancy: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3546435/ https://www.ncbi.nlm.nih.gov/pubmed/23346435 http://dx.doi.org/10.1155/2012/859068 |
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