Mid-aortic syndrome presented as dilated cardiomyopathy

Mid-aortic syndrome (MAS) is a rare vascular disease that usually leads to renovascular hypertension. With the predominant manifestations being intractable arterial hypertension and lower extremity arterial insufficiency, it has rarely been associated with dilated cardiomyopathy. We report a young g...

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Main Authors: Kah, Yit Pang, Yubbu, Putri, Ali, Norliza, Ghee, Tiong Koh
Format: Article
Published: BMJ Publishing Group 2024
Online Access:http://psasir.upm.edu.my/id/eprint/119303/
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author Kah, Yit Pang
Yubbu, Putri
Ali, Norliza
Ghee, Tiong Koh
author_facet Kah, Yit Pang
Yubbu, Putri
Ali, Norliza
Ghee, Tiong Koh
author_sort Kah, Yit Pang
building UPM Institutional Repository
collection Online Access
description Mid-aortic syndrome (MAS) is a rare vascular disease that usually leads to renovascular hypertension. With the predominant manifestations being intractable arterial hypertension and lower extremity arterial insufficiency, it has rarely been associated with dilated cardiomyopathy. We report a young girl with congestive heart failure, where the cause was initially attributed to dilated cardiomyopathy. A repeated echocardiogram 6 months later brought the physician's suspicion of MAS because of the abnormal colour of Doppler from the subcostal view. Further assessment using CT angiography revealed discrete thoracic coarctation at the level of T10, with the narrowest diameter of 2.1 mm, thus confirming the diagnosis. Her inflammatory markers and connective tissue screening were negative. She underwent successful stenting of coarctation of the aorta, which later caused improvement in her cardiac function. We highlighted the importance of looking for treatable causes of dilated cardiomyopathy and vigilant clinical and echocardiogram assessment with high suspicion to diagnose MAS.
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spelling upm-1193032025-08-14T00:38:35Z http://psasir.upm.edu.my/id/eprint/119303/ Mid-aortic syndrome presented as dilated cardiomyopathy Kah, Yit Pang Yubbu, Putri Ali, Norliza Ghee, Tiong Koh Mid-aortic syndrome (MAS) is a rare vascular disease that usually leads to renovascular hypertension. With the predominant manifestations being intractable arterial hypertension and lower extremity arterial insufficiency, it has rarely been associated with dilated cardiomyopathy. We report a young girl with congestive heart failure, where the cause was initially attributed to dilated cardiomyopathy. A repeated echocardiogram 6 months later brought the physician's suspicion of MAS because of the abnormal colour of Doppler from the subcostal view. Further assessment using CT angiography revealed discrete thoracic coarctation at the level of T10, with the narrowest diameter of 2.1 mm, thus confirming the diagnosis. Her inflammatory markers and connective tissue screening were negative. She underwent successful stenting of coarctation of the aorta, which later caused improvement in her cardiac function. We highlighted the importance of looking for treatable causes of dilated cardiomyopathy and vigilant clinical and echocardiogram assessment with high suspicion to diagnose MAS. BMJ Publishing Group 2024 Article PeerReviewed Kah, Yit Pang and Yubbu, Putri and Ali, Norliza and Ghee, Tiong Koh (2024) Mid-aortic syndrome presented as dilated cardiomyopathy. BMJ Case Reports, 17 (6). art. no. e259981. ISSN 1757-790X https://casereports.bmj.com/lookup/doi/10.1136/bcr-2024-259981 10.1136/bcr-2024-259981
spellingShingle Kah, Yit Pang
Yubbu, Putri
Ali, Norliza
Ghee, Tiong Koh
Mid-aortic syndrome presented as dilated cardiomyopathy
title Mid-aortic syndrome presented as dilated cardiomyopathy
title_full Mid-aortic syndrome presented as dilated cardiomyopathy
title_fullStr Mid-aortic syndrome presented as dilated cardiomyopathy
title_full_unstemmed Mid-aortic syndrome presented as dilated cardiomyopathy
title_short Mid-aortic syndrome presented as dilated cardiomyopathy
title_sort mid-aortic syndrome presented as dilated cardiomyopathy
url http://psasir.upm.edu.my/id/eprint/119303/
http://psasir.upm.edu.my/id/eprint/119303/
http://psasir.upm.edu.my/id/eprint/119303/