ArticleJapanese journal of radiology2015
Rare case of truncus arteriosus with anomalous origin of the right coronary artery from the pulmonary artery (ARCAPA) and unilateral left pulmonary artery agenesis.
Article in Japanese journal of radiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed, 7 citations in OpenAlex.
- A rare complex association of truncus arteriosus with anomalous left coronary artery from the pulmonary artery: A case of rare congenital deformity.Radiology case reports · 2025Article
- Case report of rare congenital cardiovascular anomalies associated with truncus arteriosus type 2.Heliyon · 2022Article
- Thrombosis in the Surgically Corrected Anomalous Right Coronary Artery after Reimplantation in Aorta.Case reports in cardiology · 2017Article
- Persistent truncus arteriosus on dual source CT.Japanese journal of radiology · 2016Review
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Authors and funding
7 authors at 1 institution in 1 country.
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Abstract
The incidence of congenital heart disease (CHD) is 2.4-3.8/1000 live births. Up to 70.7 % of all cases of CHD are reported to be benign; complex heart anomalies are extremely rare. Our case is extremely rare, as we report three very rare findings-truncus arteriosus, anomalous origin of the right coronary artery from the pulmonary artery (ARCAPA), and unilateral left pulmonary artery agenesis-in a single patient. Congenital complex cardiac abnormalities are very rare, and two-dimensional echocardiography screening should be supported by cardiac computed tomography (CT). We report a case of truncus arteriosus associated with ARCAPA and left pulmonary artery agenesis diagnosed by cardiac computed tomography; we believe that such an unusual case with all three of these entities has never been reported before.
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