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...
Main Authors: | , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
SAGE Publishing
2017-07-01
|
Series: | Journal of Investigative Medicine High Impact Case Reports |
Online Access: | https://doi.org/10.1177/2324709617719917 |
id |
doaj-6fa90fbd443f45d190dcb6e3e510cc9e |
---|---|
record_format |
Article |
spelling |
doaj-6fa90fbd443f45d190dcb6e3e510cc9e2020-11-25T04:02:52ZengSAGE PublishingJournal of Investigative Medicine High Impact Case Reports2324-70962017-07-01510.1177/2324709617719917A Rare Presentation of Fibromuscular Dysplasia: Postpartum Vascular Catastrophe and Brief Literature ReviewFatima Khan MD0Ali Raza Ghani MD1Larami Mackenzie MD2Ashwin Matthew MD3Usman Sarwar MD4Bruce Klugherz MD5Department of Internal Medicine Abington Jefferson, PA, USADepartment of Internal Medicine Abington Jefferson, PA, USADepartment of Neurovascular, Abington Jefferson Jefferson Health, PA, USADrexel University Hospital, PA, USADepartment of Internal Medicine Abington Jefferson, PA, USACardiology Abington Jefferson Jefferson Health, PA, USASpontaneous 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.https://doi.org/10.1177/2324709617719917 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Fatima Khan MD Ali Raza Ghani MD Larami Mackenzie MD Ashwin Matthew MD Usman Sarwar MD Bruce Klugherz MD |
spellingShingle |
Fatima Khan MD Ali Raza Ghani MD Larami Mackenzie MD Ashwin Matthew MD Usman Sarwar MD Bruce Klugherz MD A Rare Presentation of Fibromuscular Dysplasia: Postpartum Vascular Catastrophe and Brief Literature Review Journal of Investigative Medicine High Impact Case Reports |
author_facet |
Fatima Khan MD Ali Raza Ghani MD Larami Mackenzie MD Ashwin Matthew MD Usman Sarwar MD Bruce Klugherz MD |
author_sort |
Fatima Khan MD |
title |
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_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_sort |
rare presentation of fibromuscular dysplasia: postpartum vascular catastrophe and brief literature review |
publisher |
SAGE Publishing |
series |
Journal of Investigative Medicine High Impact Case Reports |
issn |
2324-7096 |
publishDate |
2017-07-01 |
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. |
url |
https://doi.org/10.1177/2324709617719917 |
work_keys_str_mv |
AT fatimakhanmd ararepresentationoffibromusculardysplasiapostpartumvascularcatastropheandbriefliteraturereview AT alirazaghanimd ararepresentationoffibromusculardysplasiapostpartumvascularcatastropheandbriefliteraturereview AT laramimackenziemd ararepresentationoffibromusculardysplasiapostpartumvascularcatastropheandbriefliteraturereview AT ashwinmatthewmd ararepresentationoffibromusculardysplasiapostpartumvascularcatastropheandbriefliteraturereview AT usmansarwarmd ararepresentationoffibromusculardysplasiapostpartumvascularcatastropheandbriefliteraturereview AT bruceklugherzmd ararepresentationoffibromusculardysplasiapostpartumvascularcatastropheandbriefliteraturereview AT fatimakhanmd rarepresentationoffibromusculardysplasiapostpartumvascularcatastropheandbriefliteraturereview AT alirazaghanimd rarepresentationoffibromusculardysplasiapostpartumvascularcatastropheandbriefliteraturereview AT laramimackenziemd rarepresentationoffibromusculardysplasiapostpartumvascularcatastropheandbriefliteraturereview AT ashwinmatthewmd rarepresentationoffibromusculardysplasiapostpartumvascularcatastropheandbriefliteraturereview AT usmansarwarmd rarepresentationoffibromusculardysplasiapostpartumvascularcatastropheandbriefliteraturereview AT bruceklugherzmd rarepresentationoffibromusculardysplasiapostpartumvascularcatastropheandbriefliteraturereview |
_version_ |
1724441865370992640 |