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Anomalous origin of the right coronary artery from the pulmonary artery associated with an aortopulmonary window
Anomalous origin of the right coronary artery (RCA) from the pulmonary artery is a rare entity that causes chronic left-to-right shunting of blood from the RCA, through the coronary collaterals into the pulmonary artery. This results in persistent myocardial ischemia and ventricular dysfunction. Ass...
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Published in: | Annals of pediatric cardiology 2018-09, Vol.11 (3), p.325-327 |
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creator | Bhat, Padebettu Chandrashekar, Chandana Mallikarjun, Divya Girish Gowda, S |
description | Anomalous origin of the right coronary artery (RCA) from the pulmonary artery is a rare entity that causes chronic left-to-right shunting of blood from the RCA, through the coronary collaterals into the pulmonary artery. This results in persistent myocardial ischemia and ventricular dysfunction. Association of this anomaly with an aortopulmonary window worsens the condition further due to an additional shunt. We encountered a combination of these two anomalies along with an ostium secundum atrial septal defect in a 10-month-old baby who presented with excessive crying and failure to thrive. Evaluation by transthoracic echocardiography and cardiac computed tomography scan confirmed the diagnosis. Intrapulmonary baffle was done using a pericardial patch to connect the RCA origin to ascending aorta through the aortopulmonary window, similar to Takeuchi procedure. Concomitantly, ostium secundum atrial septal defect was also closed. |
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This results in persistent myocardial ischemia and ventricular dysfunction. Association of this anomaly with an aortopulmonary window worsens the condition further due to an additional shunt. We encountered a combination of these two anomalies along with an ostium secundum atrial septal defect in a 10-month-old baby who presented with excessive crying and failure to thrive. Evaluation by transthoracic echocardiography and cardiac computed tomography scan confirmed the diagnosis. Intrapulmonary baffle was done using a pericardial patch to connect the RCA origin to ascending aorta through the aortopulmonary window, similar to Takeuchi procedure. Concomitantly, ostium secundum atrial septal defect was also closed.</description><identifier>ISSN: 0974-2069</identifier><identifier>EISSN: 0974-5149</identifier><identifier>DOI: 10.4103/apc.APC_65_18</identifier><identifier>PMID: 30271028</identifier><language>eng</language><publisher>India: Wolters Kluwer India Pvt. Ltd</publisher><subject>Abnormalities ; Anomalous origin of the right coronary artery from the pulmonary artery ; aortopulmonary window ; Atrial septal defects ; Care and treatment ; Case studies ; Coronary arteries ; Coronary vessels ; Defects ; Electrocardiography ; intrapulmonary baffle ; Ischemia ; Pediatric cardiology ; Pulmonary arteries ; Pulmonary artery</subject><ispartof>Annals of pediatric cardiology, 2018-09, Vol.11 (3), p.325-327</ispartof><rights>COPYRIGHT 2018 Medknow Publications and Media Pvt. Ltd.</rights><rights>2018. This work is published under https://creativecommons.org/licenses/by-nc-sa/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright: © 2018 Annals of Pediatric Cardiology 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c568u-a164bb3bd357bc21b4ccc8aa918a8b9df584db9c7341c39741bbed7bdb2927e23</citedby><cites>FETCH-LOGICAL-c568u-a164bb3bd357bc21b4ccc8aa918a8b9df584db9c7341c39741bbed7bdb2927e23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6146862/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2102425296?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25730,27900,27901,36988,36989,44565,53765,53767</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30271028$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bhat, Padebettu</creatorcontrib><creatorcontrib>Chandrashekar, Chandana</creatorcontrib><creatorcontrib>Mallikarjun, Divya</creatorcontrib><creatorcontrib>Girish Gowda, S</creatorcontrib><title>Anomalous origin of the right coronary artery from the pulmonary artery associated with an aortopulmonary window</title><title>Annals of pediatric cardiology</title><addtitle>Ann Pediatr Cardiol</addtitle><description>Anomalous origin of the right coronary artery (RCA) from the pulmonary artery is a rare entity that causes chronic left-to-right shunting of blood from the RCA, through the coronary collaterals into the pulmonary artery. This results in persistent myocardial ischemia and ventricular dysfunction. Association of this anomaly with an aortopulmonary window worsens the condition further due to an additional shunt. We encountered a combination of these two anomalies along with an ostium secundum atrial septal defect in a 10-month-old baby who presented with excessive crying and failure to thrive. Evaluation by transthoracic echocardiography and cardiac computed tomography scan confirmed the diagnosis. Intrapulmonary baffle was done using a pericardial patch to connect the RCA origin to ascending aorta through the aortopulmonary window, similar to Takeuchi procedure. Concomitantly, ostium secundum atrial septal defect was also closed.</description><subject>Abnormalities</subject><subject>Anomalous origin of the right coronary artery from the pulmonary artery</subject><subject>aortopulmonary window</subject><subject>Atrial septal defects</subject><subject>Care and treatment</subject><subject>Case studies</subject><subject>Coronary arteries</subject><subject>Coronary vessels</subject><subject>Defects</subject><subject>Electrocardiography</subject><subject>intrapulmonary baffle</subject><subject>Ischemia</subject><subject>Pediatric cardiology</subject><subject>Pulmonary arteries</subject><subject>Pulmonary artery</subject><issn>0974-2069</issn><issn>0974-5149</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkktvEzEUhUcIREthyRaNhITYpPg1tmdDFUU8KlWCBayt60cyk3rsYM8w4t_jNGmgiJUf99Pxudenql5idMkwou9gZy6XX1eKNwrLR9U5agVbNJi1j497gnh7Vj3LeYsQZ4Swp9UZRURgROR5tVuGOICPU65j6jd9qOO6HjtXl0M31iamGCD9qiGNrizrFIe78m7yw4MK5BxND6Oz9dyPXQ2hhpjG-Aec-2Dj_Lx6sgaf3YvjelF9__jh2-rz4ubLp-vV8mZhGi6nBWDOtKba0kZoQ7BmxhgJ0GIJUrd23UhmdWsEZdjQ0ifW2lmhrSYtEY7Qi-r6oGsjbNUu9UPxoCL06u4ipo0qznvjnSo6mIIQ1nLCNHcapARnNefFQ3mnaL0_aO0mPThrXBgT-AeiDyuh79Qm_lQcMy753szbo0CKPyaXRzX02TjvIbgyekUwboigiPOCvv4H3cYphTKqQiHCSEPaPfXmQG2gNNA58GOXo5_GPoaslk1DpRCM4QIuDqBJMefk1ifXGKl9gFQJkDoFqPCv_m71RN8npgBXB2COvnx8vvXT7JIq7G2I8_9VFSWNug8a_Q2US9sZ</recordid><startdate>20180901</startdate><enddate>20180901</enddate><creator>Bhat, Padebettu</creator><creator>Chandrashekar, Chandana</creator><creator>Mallikarjun, Divya</creator><creator>Girish Gowda, S</creator><general>Wolters Kluwer India Pvt. 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This results in persistent myocardial ischemia and ventricular dysfunction. Association of this anomaly with an aortopulmonary window worsens the condition further due to an additional shunt. We encountered a combination of these two anomalies along with an ostium secundum atrial septal defect in a 10-month-old baby who presented with excessive crying and failure to thrive. Evaluation by transthoracic echocardiography and cardiac computed tomography scan confirmed the diagnosis. Intrapulmonary baffle was done using a pericardial patch to connect the RCA origin to ascending aorta through the aortopulmonary window, similar to Takeuchi procedure. Concomitantly, ostium secundum atrial septal defect was also closed.</abstract><cop>India</cop><pub>Wolters Kluwer India Pvt. Ltd</pub><pmid>30271028</pmid><doi>10.4103/apc.APC_65_18</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Abnormalities Anomalous origin of the right coronary artery from the pulmonary artery aortopulmonary window Atrial septal defects Care and treatment Case studies Coronary arteries Coronary vessels Defects Electrocardiography intrapulmonary baffle Ischemia Pediatric cardiology Pulmonary arteries Pulmonary artery |
title | Anomalous origin of the right coronary artery from the pulmonary artery associated with an aortopulmonary window |
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