Large isolated major aortopulmonary collateral artery causing dilated left ventricle
Isolated major aortopulmonary collateral artery (MAPCA), in the absence of evidence of structural heart disease, is a very rare observation. This anomaly usually appears in preterm newborns. In the majority of babies, isolated MAPCAs cause no symptoms and regress spontaneously after birth and their...
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Format: | Article |
Language: | English |
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Elsevier
2023-04-01
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Series: | Radiology Case Reports |
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Online Access: | http://www.sciencedirect.com/science/article/pii/S1930043323000638 |
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author | Le Xuan Hoang, MD Le Kim Tuyen, MD Tran Minh Gia, MD Ngo-Thi Kim Anh, MD Do-Van Buu Dan, MD Phan Kim Phuong, MD Do Nguyen Tin, MD Tran Hoa, MD Nguyen Minh Duc, MD |
author_facet | Le Xuan Hoang, MD Le Kim Tuyen, MD Tran Minh Gia, MD Ngo-Thi Kim Anh, MD Do-Van Buu Dan, MD Phan Kim Phuong, MD Do Nguyen Tin, MD Tran Hoa, MD Nguyen Minh Duc, MD |
author_sort | Le Xuan Hoang, MD |
collection | DOAJ |
description | Isolated major aortopulmonary collateral artery (MAPCA), in the absence of evidence of structural heart disease, is a very rare observation. This anomaly usually appears in preterm newborns. In the majority of babies, isolated MAPCAs cause no symptoms and regress spontaneously after birth and their conservative management is usually sufficient. We report a case of an asymptomatic full-term 5-month-old infant presenting with heart murmur as the only sign during clinical evaluation. Echocardiography revealed a dilated left ventricle, with no pulmonary hypertension. Computed tomography angiogram showed a large MAPCA arising from the descending thoracic aorta and supplying blood to the left lower lobe. The condition was managed successfully by percutaneous obliteration with Amplatzer vascular plugs. Isolated MAPCA is usually a benign anomaly, presenting no clinical finding and requiring no specific treatment. However, in a small minority of infants, this congenital disorder may progress, with detrimental impacts on cardiac structure before clinical symptoms appear. Early intervention may be required to prevent irreversible sequelae. |
first_indexed | 2024-04-10T07:17:41Z |
format | Article |
id | doaj.art-a0d1c78f63e745a4a5057e34f6175bf0 |
institution | Directory Open Access Journal |
issn | 1930-0433 |
language | English |
last_indexed | 2024-04-10T07:17:41Z |
publishDate | 2023-04-01 |
publisher | Elsevier |
record_format | Article |
series | Radiology Case Reports |
spelling | doaj.art-a0d1c78f63e745a4a5057e34f6175bf02023-02-25T04:09:49ZengElsevierRadiology Case Reports1930-04332023-04-0118415301535Large isolated major aortopulmonary collateral artery causing dilated left ventricleLe Xuan Hoang, MD0Le Kim Tuyen, MD1Tran Minh Gia, MD2Ngo-Thi Kim Anh, MD3Do-Van Buu Dan, MD4Phan Kim Phuong, MD5Do Nguyen Tin, MD6Tran Hoa, MD7Nguyen Minh Duc, MD8Tam Duc Heart Hospital, Ho Chi Minh City, VietnamTam Duc Heart Hospital, Ho Chi Minh City, Vietnam; Pham Ngoc Thach University of Medicine, 2 Duong Quang Trung Ward 12 District 10, Ho Chi Minh City, VietnamTam Duc Heart Hospital, Ho Chi Minh City, VietnamTam Duc Heart Hospital, Ho Chi Minh City, VietnamTam Duc Heart Hospital, Ho Chi Minh City, VietnamTam Duc Heart Hospital, Ho Chi Minh City, VietnamChildren's Hospital 1, Ho Chi Minh City, Vietnam; University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City, VietnamUniversity of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City, VietnamPham Ngoc Thach University of Medicine, 2 Duong Quang Trung Ward 12 District 10, Ho Chi Minh City, Vietnam; Corresponding author.Isolated major aortopulmonary collateral artery (MAPCA), in the absence of evidence of structural heart disease, is a very rare observation. This anomaly usually appears in preterm newborns. In the majority of babies, isolated MAPCAs cause no symptoms and regress spontaneously after birth and their conservative management is usually sufficient. We report a case of an asymptomatic full-term 5-month-old infant presenting with heart murmur as the only sign during clinical evaluation. Echocardiography revealed a dilated left ventricle, with no pulmonary hypertension. Computed tomography angiogram showed a large MAPCA arising from the descending thoracic aorta and supplying blood to the left lower lobe. The condition was managed successfully by percutaneous obliteration with Amplatzer vascular plugs. Isolated MAPCA is usually a benign anomaly, presenting no clinical finding and requiring no specific treatment. However, in a small minority of infants, this congenital disorder may progress, with detrimental impacts on cardiac structure before clinical symptoms appear. Early intervention may be required to prevent irreversible sequelae.http://www.sciencedirect.com/science/article/pii/S1930043323000638Isolated major aortopulmonary collateral arteryAmplatzer vascular plugsClosureAsymptomatic |
spellingShingle | Le Xuan Hoang, MD Le Kim Tuyen, MD Tran Minh Gia, MD Ngo-Thi Kim Anh, MD Do-Van Buu Dan, MD Phan Kim Phuong, MD Do Nguyen Tin, MD Tran Hoa, MD Nguyen Minh Duc, MD Large isolated major aortopulmonary collateral artery causing dilated left ventricle Radiology Case Reports Isolated major aortopulmonary collateral artery Amplatzer vascular plugs Closure Asymptomatic |
title | Large isolated major aortopulmonary collateral artery causing dilated left ventricle |
title_full | Large isolated major aortopulmonary collateral artery causing dilated left ventricle |
title_fullStr | Large isolated major aortopulmonary collateral artery causing dilated left ventricle |
title_full_unstemmed | Large isolated major aortopulmonary collateral artery causing dilated left ventricle |
title_short | Large isolated major aortopulmonary collateral artery causing dilated left ventricle |
title_sort | large isolated major aortopulmonary collateral artery causing dilated left ventricle |
topic | Isolated major aortopulmonary collateral artery Amplatzer vascular plugs Closure Asymptomatic |
url | http://www.sciencedirect.com/science/article/pii/S1930043323000638 |
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