<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(5)</volume><submitter>Alghamdi FA</submitter><pubmed_abstract>&lt;h4>Background&lt;/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.&lt;h4>Case summary&lt;/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</pubmed_abstract><journal>European heart journal. Case reports</journal><pagination>ytad230</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10180372</full_dataset_link><repository>biostudies-literature</repository><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.</pubmed_title><pmcid>PMC10180372</pmcid><pubmed_authors>Alghamdi FA</pubmed_authors><pubmed_authors>Alkhodair AM</pubmed_authors><pubmed_authors>Alshalash S</pubmed_authors><pubmed_authors>Shah MA</pubmed_authors></additional><is_claimable>false</is_claimable><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.</name><description>&lt;h4>Background&lt;/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.&lt;h4>Case summary&lt;/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</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 May</publication><modification>2025-04-25T22:31:01.622Z</modification><creation>2025-04-06T09:03:24.74Z</creation></dates><accession>S-EPMC10180372</accession><cross_references><pubmed>37187973</pubmed><doi>10.1093/ehjcr/ytad230</doi></cross_references></HashMap>