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A Rare Presentation of Fibromuscular Dysplasia: Postpartum Vascular Catastrophe and Brief Literature Review

Spontaneous coronary artery dissection is a very rare cause of acute coronary syndromes and can be life threatening given the rarity of the condition. It should be part of differentials in young females presenting with acute coronary syndromes without routine risk factors for coronary artery disease...

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Autores principales: Khan, Fatima, Ghani, Ali Raza, Mackenzie, Larami, Matthew, Ashwin, Sarwar, Usman, Klugherz, Bruce
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5542092/
https://www.ncbi.nlm.nih.gov/pubmed/28815187
http://dx.doi.org/10.1177/2324709617719917
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author Khan, Fatima
Ghani, Ali Raza
Mackenzie, Larami
Matthew, Ashwin
Sarwar, Usman
Klugherz, Bruce
author_facet Khan, Fatima
Ghani, Ali Raza
Mackenzie, Larami
Matthew, Ashwin
Sarwar, Usman
Klugherz, Bruce
author_sort Khan, Fatima
collection PubMed
description Spontaneous coronary artery dissection is a very rare cause of acute coronary syndromes and can be life threatening given the rarity of the condition. It should be part of differentials in young females presenting with acute coronary syndromes without routine risk factors for coronary artery disease, especially before, during, and after pregnancy. It is closely associated with fibromuscular dysplasia and management can be very challenging at times. We present a case of spontaneous coronary artery dissection presenting with recurrent ST segment elevation myocardial infarction in association with fibromuscular dysplasia.
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spelling pubmed-55420922017-08-16 A Rare Presentation of Fibromuscular Dysplasia: Postpartum Vascular Catastrophe and Brief Literature Review Khan, Fatima Ghani, Ali Raza Mackenzie, Larami Matthew, Ashwin Sarwar, Usman Klugherz, Bruce J Investig Med High Impact Case Rep Case Report Spontaneous coronary artery dissection is a very rare cause of acute coronary syndromes and can be life threatening given the rarity of the condition. It should be part of differentials in young females presenting with acute coronary syndromes without routine risk factors for coronary artery disease, especially before, during, and after pregnancy. It is closely associated with fibromuscular dysplasia and management can be very challenging at times. We present a case of spontaneous coronary artery dissection presenting with recurrent ST segment elevation myocardial infarction in association with fibromuscular dysplasia. SAGE Publications 2017-07-31 /pmc/articles/PMC5542092/ /pubmed/28815187 http://dx.doi.org/10.1177/2324709617719917 Text en © 2017 American Federation for Medical Research http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution 4.0 License (http://www.creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Khan, Fatima
Ghani, Ali Raza
Mackenzie, Larami
Matthew, Ashwin
Sarwar, Usman
Klugherz, Bruce
A Rare Presentation of Fibromuscular Dysplasia: Postpartum Vascular Catastrophe and Brief Literature Review
title A Rare Presentation of Fibromuscular Dysplasia: Postpartum Vascular Catastrophe and Brief Literature Review
title_full A Rare Presentation of Fibromuscular Dysplasia: Postpartum Vascular Catastrophe and Brief Literature Review
title_fullStr A Rare Presentation of Fibromuscular Dysplasia: Postpartum Vascular Catastrophe and Brief Literature Review
title_full_unstemmed A Rare Presentation of Fibromuscular Dysplasia: Postpartum Vascular Catastrophe and Brief Literature Review
title_short A Rare Presentation of Fibromuscular Dysplasia: Postpartum Vascular Catastrophe and Brief Literature Review
title_sort rare presentation of fibromuscular dysplasia: postpartum vascular catastrophe and brief literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5542092/
https://www.ncbi.nlm.nih.gov/pubmed/28815187
http://dx.doi.org/10.1177/2324709617719917
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