Skip to main content Accessibility help
×
Home
Hostname: page-component-65dc7cd545-8rn5k Total loading time: 0.15 Render date: 2021-07-26T05:57:51.495Z Has data issue: true Feature Flags: { "shouldUseShareProductTool": true, "shouldUseHypothesis": true, "isUnsiloEnabled": true, "metricsAbstractViews": false, "figures": true, "newCiteModal": false, "newCitedByModal": true, "newEcommerce": true, "newUsageEvents": true }

Aortopulmonary window with anomalous origin of the right coronary artery from the pulmonary trunk

Published online by Cambridge University Press:  11 January 2021

Atakan Atalay
Affiliation:
Ankara City Hospital, Department of Pediatric Cardiovascular Surgery, Ankara, Turkey
Başak Soran Turkcan
Affiliation:
Ankara City Hospital, Department of Pediatric Cardiovascular Surgery, Ankara, Turkey
Emre Kulahcioglu
Affiliation:
Ankara City Hospital, Department of Pediatric Cardiovascular Surgery, Ankara, Turkey
Deniz Eris
Affiliation:
Isparta City Hospital, Department of Pediatric Cardiology, Isparta, Turkey
İbrahim Ece
Affiliation:
Ankara City Hospital, Department of Neonatology, Ankara, Turkey
Hakan Aydın
Affiliation:
Ankara City Hospital, Department of Pediatric Cardiovascular Surgery, Ankara, Turkey
Corresponding
E-mail address:

Abstract

Anomalous origin of coronary artery originating from the pulmonary artery in conjunction with the aorticopulmonary window (APW) is a rare but a significant anomaly in the era of congenital cardiac diseases. The occurrence of anomalous origin of the right coronary artery from the pulmonary artery among the associated anomalies is less than 5%. The severity of the clinical condition of these patients depends on the degree of left–right shunt and compromise of the pulmonary blood flow. We report surgical management of a case of a 45-day-old infant with APW, ventricular septal defect, and anomalous origin of coronary artery originated from the pulmonary artery.

Type
Brief Report
Copyright
© The Author(s), 2021. Published by Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below.

References

Izumoto, H, Ishihara, K, Fujii, Y, Oyama, K, Kawazoe, K. AP window and anomalous origin of right coronary artery from the window. Ann Thorac Surg 1999; 68: 557559.Google ScholarPubMed
Kutcche, LM, Van Meirop, LH. Anatomy and pathogenesis of aorticopulmonary septal defect. Ann J Cardiol 1987; 59: 443447.Google Scholar
Kirklin, JW, Barratt-Boyes, BG. Coarctation of the aorta and interrupted aortic arch. In: Kirklin, JW, Barratt-Boyes, BG (eds). Cardiac Surgery, 2nd edn. Churchill Livingston, Inc; New York, 1993: 12631326.Google ScholarPubMed
Bockeria, LA, Berishvili, DO, Krupianko, SM, et al. Anomalous origin of the right coronary artery from the pulmonary artery with aortopulmonary window. World J Pediatr Congenit Heart Surg 2010; 1: 254258.Google ScholarPubMed
Morell, VO, Feccia, M, Cullen, S, Elliott, MJ Anomalous coronary artery with tetralogy of Fallot and aortopulmonary window. Ann Thorac Surg 1998;66:1403–5.Google ScholarPubMed
Jiten, S, Manpal, L, Alok, S, Manoranjan, S, Tek S, M. Aortopulmonary window with anomalous coronary arteries. J Card Surg 2015; 30: 846848.Google Scholar
Kumar, V, Singh, RS, Thingnam, SKS, Mishra, AK, Jaswal, V. Surgical outcome in aortopulmonary window beyond the neonatal period. J Card Surg 2019; 34: 300304.Google ScholarPubMed
Alakhfash, AA, Tagelden, M, Almesned, A, Alqwaiee, A. (2020) Aortopulmonary window with anomalous right coronary artery from the pulmonary artery. Case report and literature review. Cardiol Young 2020; 30: 4749.Google ScholarPubMed
Gabbieri, D, Guadalupi, M, Stefanelli, G. Aortopulmoner window and anomalous Origin of the right coronary artery from the pulmonary artery: long-term result after Takeuchi-Type repair. Heart Lung Circ 2008;17: 330351.Google Scholar
Dodge-Khatami, A, Mavroudis, C, Backer, CL. Anomalous origin of the left coronary artery from the pulmonary artery: collective review of surgical therapy. Ann Thorac Surg 2002; 74: 946955.Google ScholarPubMed

Send article to Kindle

To send this article to your Kindle, first ensure no-reply@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about sending to your Kindle. Find out more about sending to your Kindle.

Note you can select to send to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be sent to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Aortopulmonary window with anomalous origin of the right coronary artery from the pulmonary trunk
Available formats
×

Send article to Dropbox

To send this article to your Dropbox account, please select one or more formats and confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your <service> account. Find out more about sending content to Dropbox.

Aortopulmonary window with anomalous origin of the right coronary artery from the pulmonary trunk
Available formats
×

Send article to Google Drive

To send this article to your Google Drive account, please select one or more formats and confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your <service> account. Find out more about sending content to Google Drive.

Aortopulmonary window with anomalous origin of the right coronary artery from the pulmonary trunk
Available formats
×
×

Reply to: Submit a response

Please enter your response.

Your details

Please enter a valid email address.

Conflicting interests

Do you have any conflicting interests? *