Cargando…

An aortopathy dilemma in pregnancy: A rare case report

BACKGROUND: The most dramatic diseases in the aorta are aortic dissection and aneurysm, which both of them are common in pregnant women with Marfan syndrome (MFS). According to recommendations in existing guidelines, pregnancy is not recommended in patients with severe dilation of the aorta and pati...

Descripción completa

Detalles Bibliográficos
Autores principales: Saeidi, Mahmoud, Movahedi, Minoo, Bahrami, Parvin, Shokrani-Foroushani, Reza, Sheikhbahaei, Erfan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Isfahan Cardiovascular Research Center, Isfahan University of Medical Sciences 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635720/
https://www.ncbi.nlm.nih.gov/pubmed/36338528
http://dx.doi.org/10.22122/arya.v17i0.2110
_version_ 1784824770424995840
author Saeidi, Mahmoud
Movahedi, Minoo
Bahrami, Parvin
Shokrani-Foroushani, Reza
Sheikhbahaei, Erfan
author_facet Saeidi, Mahmoud
Movahedi, Minoo
Bahrami, Parvin
Shokrani-Foroushani, Reza
Sheikhbahaei, Erfan
author_sort Saeidi, Mahmoud
collection PubMed
description BACKGROUND: The most dramatic diseases in the aorta are aortic dissection and aneurysm, which both of them are common in pregnant women with Marfan syndrome (MFS). According to recommendations in existing guidelines, pregnancy is not recommended in patients with severe dilation of the aorta and patients with MFS with aortic dilation > 45 mm should have prophylactic aortic repair before pregnancy. CASE REPORT: In this rare and unique report, we described a 34-year-old pregnant woman with marfanoid feature who had an approximate aortic root of 60 mm and severe aortic insufficiency. She denied terminating the pregnancy at her first prenatal visit and continued it until 30 weeks of gestation and the pregnancy terminated in the cardiac operating room due to multiple episodes of chest pain. No complication occurred during her close observation before surgery. The aortic repair was performed for her after the cesarean section. CONCLUSION: Pregnancy with severe aortic root dilation is high-risk for all patients; however, if it occurs, when the mother denies an abortion, inform the patient about its risk and continue the pregnancy with close observation and tight blood pressure (BP) control until the fetus becomes viable.
format Online
Article
Text
id pubmed-9635720
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Isfahan Cardiovascular Research Center, Isfahan University of Medical Sciences
record_format MEDLINE/PubMed
spelling pubmed-96357202022-11-04 An aortopathy dilemma in pregnancy: A rare case report Saeidi, Mahmoud Movahedi, Minoo Bahrami, Parvin Shokrani-Foroushani, Reza Sheikhbahaei, Erfan ARYA Atheroscler Case Report BACKGROUND: The most dramatic diseases in the aorta are aortic dissection and aneurysm, which both of them are common in pregnant women with Marfan syndrome (MFS). According to recommendations in existing guidelines, pregnancy is not recommended in patients with severe dilation of the aorta and patients with MFS with aortic dilation > 45 mm should have prophylactic aortic repair before pregnancy. CASE REPORT: In this rare and unique report, we described a 34-year-old pregnant woman with marfanoid feature who had an approximate aortic root of 60 mm and severe aortic insufficiency. She denied terminating the pregnancy at her first prenatal visit and continued it until 30 weeks of gestation and the pregnancy terminated in the cardiac operating room due to multiple episodes of chest pain. No complication occurred during her close observation before surgery. The aortic repair was performed for her after the cesarean section. CONCLUSION: Pregnancy with severe aortic root dilation is high-risk for all patients; however, if it occurs, when the mother denies an abortion, inform the patient about its risk and continue the pregnancy with close observation and tight blood pressure (BP) control until the fetus becomes viable. Isfahan Cardiovascular Research Center, Isfahan University of Medical Sciences 2021-03 /pmc/articles/PMC9635720/ /pubmed/36338528 http://dx.doi.org/10.22122/arya.v17i0.2110 Text en © 2021 Isfahan Cardiovascular Research Center & Isfahan University of Medical Sciences https://creativecommons.org/licenses/by-nc/3.0/This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.
spellingShingle Case Report
Saeidi, Mahmoud
Movahedi, Minoo
Bahrami, Parvin
Shokrani-Foroushani, Reza
Sheikhbahaei, Erfan
An aortopathy dilemma in pregnancy: A rare case report
title An aortopathy dilemma in pregnancy: A rare case report
title_full An aortopathy dilemma in pregnancy: A rare case report
title_fullStr An aortopathy dilemma in pregnancy: A rare case report
title_full_unstemmed An aortopathy dilemma in pregnancy: A rare case report
title_short An aortopathy dilemma in pregnancy: A rare case report
title_sort aortopathy dilemma in pregnancy: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635720/
https://www.ncbi.nlm.nih.gov/pubmed/36338528
http://dx.doi.org/10.22122/arya.v17i0.2110
work_keys_str_mv AT saeidimahmoud anaortopathydilemmainpregnancyararecasereport
AT movahediminoo anaortopathydilemmainpregnancyararecasereport
AT bahramiparvin anaortopathydilemmainpregnancyararecasereport
AT shokraniforoushanireza anaortopathydilemmainpregnancyararecasereport
AT sheikhbahaeierfan anaortopathydilemmainpregnancyararecasereport
AT saeidimahmoud aortopathydilemmainpregnancyararecasereport
AT movahediminoo aortopathydilemmainpregnancyararecasereport
AT bahramiparvin aortopathydilemmainpregnancyararecasereport
AT shokraniforoushanireza aortopathydilemmainpregnancyararecasereport
AT sheikhbahaeierfan aortopathydilemmainpregnancyararecasereport