An Unusual Congenital Heart Disease: Giant Left Atrial Appendage

A 52-year-old female was admitted to our hospital in April 2021 with dyspnea. She was discharged from the hospital 3 weeks ago due to the diagnosis of pneumonia caused by coronavirus disease 2019 (COVID-19). Physical examination revealed an oxygen desaturation of 82%. The patient underwent computed...

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Main Authors: Julio C. Sauza-Sosa, Erika L. De la Cruz-Reyna, Carlos N. Velazquez-Gutierrez
Format: Article
Language:English
Published: Houston Methodist DeBakey Heart & Vascular Center 2022-03-01
Series:Methodist DeBakey Cardiovascular Journal
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Online Access:https://account.journal.houstonmethodist.org/index.php/up-j-mdbcj/article/view/1059
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author Julio C. Sauza-Sosa
Erika L. De la Cruz-Reyna
Carlos N. Velazquez-Gutierrez
author_facet Julio C. Sauza-Sosa
Erika L. De la Cruz-Reyna
Carlos N. Velazquez-Gutierrez
author_sort Julio C. Sauza-Sosa
collection DOAJ
description A 52-year-old female was admitted to our hospital in April 2021 with dyspnea. She was discharged from the hospital 3 weeks ago due to the diagnosis of pneumonia caused by coronavirus disease 2019 (COVID-19). Physical examination revealed an oxygen desaturation of 82%. The patient underwent computed tomography angiography (CTA) that showed a ground-glass pattern and a giant left atrial appendage (Figure 1A). Film array respiratory panel was negative, and pulmonary aspergillosis was diagnosed after bronchoscopy. Cardiac magnetic resonance corroborated the huge left atrial appendage (Figure 1B). No other structural or functional heart abnormalities were diagnosed. A giant left atrial appendage is a rare cardiac anomaly that can be congenital or acquired. In the literature, it is called a left atrial appendage aneurysm. The dilatation can be generalized or focused. Although it can occur in all age groups, it is predominant in patients in their 30s to 50s and most common in females.1 Patients can be asymptomatic or present with symptoms such as palpitations, chest pain, or dyspnea. A number of recent cases in the literature have highlighted the diagnostic utility of CTA.2 While there is no standard treatment for this condition, surgical resection is the most frequent therapy. Another option reported in the literature is anticoagulant treatment for select cases.3 Closure of the left atrial appendage is a more recent and emerging intervention that can be considered. In our patient, we initiated anticoagulant therapy to reduce the risk of thromboembolic events; however, we recommended left atrial appendage occlusion or surgical resection after completing the treatment for pulmonary aspergillosis.
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spelling doaj-art-ca1e694122ce44bb9b06a851328ab6d22025-08-20T02:33:23ZengHouston Methodist DeBakey Heart & Vascular CenterMethodist DeBakey Cardiovascular Journal1947-61082022-03-0118210610710.14797/mdcvj.1059812An Unusual Congenital Heart Disease: Giant Left Atrial AppendageJulio C. Sauza-Sosa0https://orcid.org/0000-0002-8708-7254Erika L. De la Cruz-Reyna1https://orcid.org/0000-0003-4246-7840Carlos N. Velazquez-Gutierrez2https://orcid.org/0000-0002-5628-7413Centro Hospitalario MAC Periferico Sur, Mexico CityCentro Hospitalario MAC Periferico Sur, Mexico CityCentro Hospitalario MAC Periferico Sur, Mexico CityA 52-year-old female was admitted to our hospital in April 2021 with dyspnea. She was discharged from the hospital 3 weeks ago due to the diagnosis of pneumonia caused by coronavirus disease 2019 (COVID-19). Physical examination revealed an oxygen desaturation of 82%. The patient underwent computed tomography angiography (CTA) that showed a ground-glass pattern and a giant left atrial appendage (Figure 1A). Film array respiratory panel was negative, and pulmonary aspergillosis was diagnosed after bronchoscopy. Cardiac magnetic resonance corroborated the huge left atrial appendage (Figure 1B). No other structural or functional heart abnormalities were diagnosed. A giant left atrial appendage is a rare cardiac anomaly that can be congenital or acquired. In the literature, it is called a left atrial appendage aneurysm. The dilatation can be generalized or focused. Although it can occur in all age groups, it is predominant in patients in their 30s to 50s and most common in females.1 Patients can be asymptomatic or present with symptoms such as palpitations, chest pain, or dyspnea. A number of recent cases in the literature have highlighted the diagnostic utility of CTA.2 While there is no standard treatment for this condition, surgical resection is the most frequent therapy. Another option reported in the literature is anticoagulant treatment for select cases.3 Closure of the left atrial appendage is a more recent and emerging intervention that can be considered. In our patient, we initiated anticoagulant therapy to reduce the risk of thromboembolic events; however, we recommended left atrial appendage occlusion or surgical resection after completing the treatment for pulmonary aspergillosis.https://account.journal.houstonmethodist.org/index.php/up-j-mdbcj/article/view/1059congenital heart diseaseleft atrial appendage
spellingShingle Julio C. Sauza-Sosa
Erika L. De la Cruz-Reyna
Carlos N. Velazquez-Gutierrez
An Unusual Congenital Heart Disease: Giant Left Atrial Appendage
Methodist DeBakey Cardiovascular Journal
congenital heart disease
left atrial appendage
title An Unusual Congenital Heart Disease: Giant Left Atrial Appendage
title_full An Unusual Congenital Heart Disease: Giant Left Atrial Appendage
title_fullStr An Unusual Congenital Heart Disease: Giant Left Atrial Appendage
title_full_unstemmed An Unusual Congenital Heart Disease: Giant Left Atrial Appendage
title_short An Unusual Congenital Heart Disease: Giant Left Atrial Appendage
title_sort unusual congenital heart disease giant left atrial appendage
topic congenital heart disease
left atrial appendage
url https://account.journal.houstonmethodist.org/index.php/up-j-mdbcj/article/view/1059
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