Cardiac leiomyomatosis misdiagnosed initially as submissive pulmonary embolism: a rare case report

This case report presents a rare case of cardiac leiomyomatosis misdiagnosed initially as submassive pulmonary embolism in a 39-year-old woman. The patient presented with syncope and hypotension, leading to an initial diagnosis of submassive pulmonary embolism. However, further investigations reveal...

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Main Author: Abdulmajeed Faleh Alosail
Format: Article
Language:English
Published: SMC MEDIA SRL 2023-11-01
Series:European Journal of Case Reports in Internal Medicine
Subjects:
Online Access:https://www.ejcrim.com/index.php/EJCRIM/article/view/4173
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author Abdulmajeed Faleh Alosail
author_facet Abdulmajeed Faleh Alosail
author_sort Abdulmajeed Faleh Alosail
collection DOAJ
description This case report presents a rare case of cardiac leiomyomatosis misdiagnosed initially as submassive pulmonary embolism in a 39-year-old woman. The patient presented with syncope and hypotension, leading to an initial diagnosis of submassive pulmonary embolism. However, further investigations revealed a right-sided heart mass on echocardiogram. Surgical intervention was carried out, and the patient’s condition was successfully managed. This case emphasizes the importance of considering rare cardiac tumours in the differential diagnosis of pulmonary embolism.
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spelling doaj.art-c492cc850cc2487cb950ecd37ccdb26d2023-12-05T10:10:16ZengSMC MEDIA SRLEuropean Journal of Case Reports in Internal Medicine2284-25942023-11-0110.12890/2023_0041733708Cardiac leiomyomatosis misdiagnosed initially as submissive pulmonary embolism: a rare case reportAbdulmajeed Faleh Alosail0Department of Internal Medicine, College of Medicine, King Faisal University, Al-Hasa, Saudi Arabia; Department of Cardiology, University of British Columbia, Vancouver, CanadaThis case report presents a rare case of cardiac leiomyomatosis misdiagnosed initially as submassive pulmonary embolism in a 39-year-old woman. The patient presented with syncope and hypotension, leading to an initial diagnosis of submassive pulmonary embolism. However, further investigations revealed a right-sided heart mass on echocardiogram. Surgical intervention was carried out, and the patient’s condition was successfully managed. This case emphasizes the importance of considering rare cardiac tumours in the differential diagnosis of pulmonary embolism.https://www.ejcrim.com/index.php/EJCRIM/article/view/4173type a aortic dissectionbentall procedureatypical symptoms
spellingShingle Abdulmajeed Faleh Alosail
Cardiac leiomyomatosis misdiagnosed initially as submissive pulmonary embolism: a rare case report
European Journal of Case Reports in Internal Medicine
type a aortic dissection
bentall procedure
atypical symptoms
title Cardiac leiomyomatosis misdiagnosed initially as submissive pulmonary embolism: a rare case report
title_full Cardiac leiomyomatosis misdiagnosed initially as submissive pulmonary embolism: a rare case report
title_fullStr Cardiac leiomyomatosis misdiagnosed initially as submissive pulmonary embolism: a rare case report
title_full_unstemmed Cardiac leiomyomatosis misdiagnosed initially as submissive pulmonary embolism: a rare case report
title_short Cardiac leiomyomatosis misdiagnosed initially as submissive pulmonary embolism: a rare case report
title_sort cardiac leiomyomatosis misdiagnosed initially as submissive pulmonary embolism a rare case report
topic type a aortic dissection
bentall procedure
atypical symptoms
url https://www.ejcrim.com/index.php/EJCRIM/article/view/4173
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