{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["7(5)"],"submitter":["Alghamdi FA"],"pubmed_abstract":["<h4>Background</h4>Anomalous origin of the coronary artery from the pulmonary artery (ALCAPA) is a rare congenital disease. Surgical re-implantation of the left main coronary artery (LMCA) to the aorta is a definitive treatment with a good prognosis.<h4>Case summary</h4>A 9-year-old boy was admitted with a complaint of exertional chest pain and dyspnoea. At 13 months of age, he was diagnosed to have ALCAPA as a workup of severe left ventricular systolic dysfunction and underwent coronary re-implantation of ALCAPA. Coronary angiogram displayed the high takeoff of re-implanted LMCA with significant ostial stenosis, and echocardiogram showed significant supravalvular pulmonary stenosis (SVPS) with a peak gradient of 74 mmHg. After a multidisciplinary team discussion, he underwent percutaneous"],"journal":["European heart journal. Case reports"],"pagination":["ytad230"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC10180372"],"repository":["biostudies-literature"],"pubmed_title":["Ostial stenosis of reimplanted left main coronary artery and supravalvular pulmonary stenosis: a case report of two complications of surgery for anomalous left coronary artery from the pulmonary artery."],"pmcid":["PMC10180372"],"pubmed_authors":["Alghamdi FA","Alkhodair AM","Alshalash S","Shah MA"],"additional_accession":[]},"is_claimable":false,"name":"Ostial stenosis of reimplanted left main coronary artery and supravalvular pulmonary stenosis: a case report of two complications of surgery for anomalous left coronary artery from the pulmonary artery.","description":"<h4>Background</h4>Anomalous origin of the coronary artery from the pulmonary artery (ALCAPA) is a rare congenital disease. Surgical re-implantation of the left main coronary artery (LMCA) to the aorta is a definitive treatment with a good prognosis.<h4>Case summary</h4>A 9-year-old boy was admitted with a complaint of exertional chest pain and dyspnoea. At 13 months of age, he was diagnosed to have ALCAPA as a workup of severe left ventricular systolic dysfunction and underwent coronary re-implantation of ALCAPA. Coronary angiogram displayed the high takeoff of re-implanted LMCA with significant ostial stenosis, and echocardiogram showed significant supravalvular pulmonary stenosis (SVPS) with a peak gradient of 74 mmHg. After a multidisciplinary team discussion, he underwent percutaneous","dates":{"release":"2023-01-01T00:00:00Z","publication":"2023 May","modification":"2025-04-25T22:31:01.622Z","creation":"2025-04-06T09:03:24.74Z"},"accession":"S-EPMC10180372","cross_references":{"pubmed":["37187973"],"doi":["10.1093/ehjcr/ytad230"]}}