Skip to main content
Top

07-11-2023 | Congenital Heart Anomaly | Case Report Free for a limited time

Aorta Without Coronary Arteries: Anatomic Variants of a Rare Malformation

Authors: Julie Karila-Cohen, Daniela Laux, Lucile Houyel, Damien Bonnet

Published in: Pediatric Cardiology

Login to get access

Abstract

Absence of connection of both coronary arteries to the aorta is an extremely rare congenital malformation. Most cases reported are anatomic variants of anomalous left coronary artery to pulmonary artery, found in isolation or in association with other congenital heart defects. We describe here four cases of patients born without any coronary artery connected to the aorta, including two with an almost complete absence of epicardial coronary arteries, one with single coronary artery to the right pulmonary artery, and one with left ventricular connection of a single coronary artery. Those exceptional coronary malformations have a poor prognosis and are often diagnosed at autopsy. Total absence of epicardial coronary arteries, present in two of our patients and described only once in the literature, leads us to reconsider current knowledge of human coronary artery development.
Literature
1.
go back to reference Ganta S, Artrip J, Schuchardt EL, Lai W, Ryan J, Nigro JJ (2022) Repair of anomalous single coronary artery from the pulmonary artery (ASCAPA). World J Pediatr Congenit Heart Surg 13(4):511–514 CrossRefPubMed Ganta S, Artrip J, Schuchardt EL, Lai W, Ryan J, Nigro JJ (2022) Repair of anomalous single coronary artery from the pulmonary artery (ASCAPA). World J Pediatr Congenit Heart Surg 13(4):511–514 CrossRefPubMed
2.
go back to reference Ochoa-Ramírez E, Valdez-Garza HE, Reyes-González R, Mateos-Corral D, Sánchez-Sigel D, González-López V (2005) Double anomalous coronary origin from the pulmonary artery: successful surgical correction in an infant. Tex Heart Inst J 32(3):348–350 PubMedPubMedCentral Ochoa-Ramírez E, Valdez-Garza HE, Reyes-González R, Mateos-Corral D, Sánchez-Sigel D, González-López V (2005) Double anomalous coronary origin from the pulmonary artery: successful surgical correction in an infant. Tex Heart Inst J 32(3):348–350 PubMedPubMedCentral
3.
go back to reference Santoro G, di Carlo D, Carotti A, Formigari R, Boldrini R, Bosman C et al (1995) Origin of both coronary arteries from the pulmonary artery and aortic coarctation. Ann Thorac Surg 60(3):706–708 CrossRefPubMed Santoro G, di Carlo D, Carotti A, Formigari R, Boldrini R, Bosman C et al (1995) Origin of both coronary arteries from the pulmonary artery and aortic coarctation. Ann Thorac Surg 60(3):706–708 CrossRefPubMed
4.
go back to reference Legendre A, Houyel L, Serraf A (2006) Severe anomaly of coronary-artery development. N Engl J Med 355(6):631–633 CrossRefPubMed Legendre A, Houyel L, Serraf A (2006) Severe anomaly of coronary-artery development. N Engl J Med 355(6):631–633 CrossRefPubMed
5.
go back to reference Bogers AJJC, Gittenberger-de Groot AC, Poelmann RE, Peault BM, Huysmans HA (1989) Development of the origin of the coronary arteries, a matter of ingrowth or outgrowth? Anat Embryol 180(5):437–441 CrossRef Bogers AJJC, Gittenberger-de Groot AC, Poelmann RE, Peault BM, Huysmans HA (1989) Development of the origin of the coronary arteries, a matter of ingrowth or outgrowth? Anat Embryol 180(5):437–441 CrossRef
6.
go back to reference Laux D, Bertail C, Bajolle F, Houyel L, Boudjemline Y, Bonnet D (2014) Anomalous left coronary artery connected to the pulmonary artery associated with other cardiac defects: a difficult joint diagnosis. Pediatr Cardiol 35(7):1198–1205 CrossRefPubMed Laux D, Bertail C, Bajolle F, Houyel L, Boudjemline Y, Bonnet D (2014) Anomalous left coronary artery connected to the pulmonary artery associated with other cardiac defects: a difficult joint diagnosis. Pediatr Cardiol 35(7):1198–1205 CrossRefPubMed
7.
go back to reference Callaghan MA, O’Hare B, Casey W (2012) What other anomalies? Failure to wean post ventricular septal defect repair secondary to anomalous origin of the left coronary artery from the pulmonary artery: failure to wean post VSD repair secondary to ALCAPA. Pediatr Anesth 22(5):487–489 CrossRef Callaghan MA, O’Hare B, Casey W (2012) What other anomalies? Failure to wean post ventricular septal defect repair secondary to anomalous origin of the left coronary artery from the pulmonary artery: failure to wean post VSD repair secondary to ALCAPA. Pediatr Anesth 22(5):487–489 CrossRef
8.
go back to reference Celik L, Becker V, Hammel D, Nürnberg JH (2010) Early detection of anomalous origin of left coronary artery from the right pulmonary artery after successful repair of critical coarctation of the aorta. Pediatr Cardiol 31(2):294–296 CrossRefPubMed Celik L, Becker V, Hammel D, Nürnberg JH (2010) Early detection of anomalous origin of left coronary artery from the right pulmonary artery after successful repair of critical coarctation of the aorta. Pediatr Cardiol 31(2):294–296 CrossRefPubMed
9.
go back to reference Pregowski J, Kaczmarska E, Kepka C, Kruk M, Dzielinska Z, Demkow M et al (2012) Single coronary artery with anomalous origin from the pulmonary trunk: congenital lack of coronary arteries originating from the aortic bulb. J Thorac Imaging 27(3):W44–W45 CrossRefPubMed Pregowski J, Kaczmarska E, Kepka C, Kruk M, Dzielinska Z, Demkow M et al (2012) Single coronary artery with anomalous origin from the pulmonary trunk: congenital lack of coronary arteries originating from the aortic bulb. J Thorac Imaging 27(3):W44–W45 CrossRefPubMed
10.
go back to reference Maskari SNA, Cochrane AD, Penny DJ (2005) Unusual cause of persistent impairment of ventricular function after repair of coarctation of the aorta. Pediatr Cardiol 26(6):836–838 CrossRefPubMed Maskari SNA, Cochrane AD, Penny DJ (2005) Unusual cause of persistent impairment of ventricular function after repair of coarctation of the aorta. Pediatr Cardiol 26(6):836–838 CrossRefPubMed
11.
go back to reference Tavora F, Burke A, Kutys R, Li L, Virmani R (2008) Total anomalous origin of the coronary circulation from the right pulmonary artery. Cardiovasc Pathol Off J Soc Cardiovasc Pathol 17(4):246–249 CrossRef Tavora F, Burke A, Kutys R, Li L, Virmani R (2008) Total anomalous origin of the coronary circulation from the right pulmonary artery. Cardiovasc Pathol Off J Soc Cardiovasc Pathol 17(4):246–249 CrossRef
12.
go back to reference Song L, Jin J, Tao L (2015) Surgical correction of an aortico-left ventricular tunnel originating from the left aortic sinus with a left coronary artery anomaly: a rare congenital heart disease. J Card Surg 30(1):108–110 CrossRefPubMed Song L, Jin J, Tao L (2015) Surgical correction of an aortico-left ventricular tunnel originating from the left aortic sinus with a left coronary artery anomaly: a rare congenital heart disease. J Card Surg 30(1):108–110 CrossRefPubMed
13.
go back to reference Wang TKM, Muniandy A, Gabriel R, van Pelt N, Harrison W, Voss J (2019) Anomalous left coronary artery originating from the left ventricular outflow tract. JACC Cardiovasc Interv 12(22):e193–e196 CrossRefPubMed Wang TKM, Muniandy A, Gabriel R, van Pelt N, Harrison W, Voss J (2019) Anomalous left coronary artery originating from the left ventricular outflow tract. JACC Cardiovasc Interv 12(22):e193–e196 CrossRefPubMed
14.
go back to reference Pirelli L, Yu PJ, Srichai MB, Khvilivitzky K, Angelini P, Grau JB (2008) Ectopic origin of left coronary ostium from left ventricle, with occlusive membrane: a previously unreported anomaly, with an embryologic interpretation. Tex Heart Inst J 35(2):162–165 PubMedPubMedCentral Pirelli L, Yu PJ, Srichai MB, Khvilivitzky K, Angelini P, Grau JB (2008) Ectopic origin of left coronary ostium from left ventricle, with occlusive membrane: a previously unreported anomaly, with an embryologic interpretation. Tex Heart Inst J 35(2):162–165 PubMedPubMedCentral
15.
go back to reference Sharma B, Chang A, Red-Horse K (2017) Coronary artery development: progenitor cells and differentiation pathways. Annu Rev Physiol 79(1):1–19 CrossRefPubMed Sharma B, Chang A, Red-Horse K (2017) Coronary artery development: progenitor cells and differentiation pathways. Annu Rev Physiol 79(1):1–19 CrossRefPubMed
16.
go back to reference Tomanek R, Angelini P (2019) Embryology of coronary arteries and anatomy/pathophysiology of coronary anomalies. A comprehensive update. Int J Cardiol 281:28–34 CrossRefPubMed Tomanek R, Angelini P (2019) Embryology of coronary arteries and anatomy/pathophysiology of coronary anomalies. A comprehensive update. Int J Cardiol 281:28–34 CrossRefPubMed
17.
18.
go back to reference Cano E, Carmona R, Ruiz-Villalba A, Rojas A, Chau YY, Wagner KD et al (2016) Extracardiac septum transversum/proepicardial endothelial cells pattern embryonic coronary arterio–venous connections. Proc Natl Acad Sci 113(3):656–661 CrossRefPubMedPubMedCentral Cano E, Carmona R, Ruiz-Villalba A, Rojas A, Chau YY, Wagner KD et al (2016) Extracardiac septum transversum/proepicardial endothelial cells pattern embryonic coronary arterio–venous connections. Proc Natl Acad Sci 113(3):656–661 CrossRefPubMedPubMedCentral
19.
go back to reference Chen HI, Poduri A, Numi H, Kivela R, Saharinen P, McKay AS et al (2014) VEGF-C and aortic cardiomyocytes guide coronary artery stem development. J Clin Invest 124(11):4899–4914 CrossRefPubMedPubMedCentral Chen HI, Poduri A, Numi H, Kivela R, Saharinen P, McKay AS et al (2014) VEGF-C and aortic cardiomyocytes guide coronary artery stem development. J Clin Invest 124(11):4899–4914 CrossRefPubMedPubMedCentral
20.
go back to reference Ivins S, Chappell J, Vernay B, Suntharalingham J, Martineau A, Mohun TJ et al (2015) The CXCL12/CXCR4 axis plays a critical role in coronary artery development. Dev Cell 33(4):455–468 CrossRefPubMedPubMedCentral Ivins S, Chappell J, Vernay B, Suntharalingham J, Martineau A, Mohun TJ et al (2015) The CXCL12/CXCR4 axis plays a critical role in coronary artery development. Dev Cell 33(4):455–468 CrossRefPubMedPubMedCentral
21.
22.
go back to reference Wessels A, Pérez-Pomares JM (2004) The epicardium and epicardially derived cells (EPDCs) as cardiac stem cells: epicardially derived cells as cardiac stem cells. Anat Rec A Discov Mol Cell Evol Biol 276A(1):43–57 CrossRef Wessels A, Pérez-Pomares JM (2004) The epicardium and epicardially derived cells (EPDCs) as cardiac stem cells: epicardially derived cells as cardiac stem cells. Anat Rec A Discov Mol Cell Evol Biol 276A(1):43–57 CrossRef
23.
go back to reference Théveniau-Ruissy M, Pérez-Pomares JM, Parisot P, Baldini A, Miquerol L, Kelly RG (2016) Coronary stem development in wild-type and Tbx1 null mouse hearts: coronary stem development in mouse hearts. Dev Dyn 245(4):445–459 CrossRefPubMed Théveniau-Ruissy M, Pérez-Pomares JM, Parisot P, Baldini A, Miquerol L, Kelly RG (2016) Coronary stem development in wild-type and Tbx1 null mouse hearts: coronary stem development in mouse hearts. Dev Dyn 245(4):445–459 CrossRefPubMed
24.
go back to reference Pérez-Pomares JM, de la Pompa JL, Franco D, Henderson D, Ho SY, Houyel L et al (2016) Congenital coronary artery anomalies: a bridge from embryology to anatomy and pathophysiology—a position statement of the development, anatomy, and pathology ESC Working Group. Cardiovasc Res 109(2):204–216 CrossRefPubMed Pérez-Pomares JM, de la Pompa JL, Franco D, Henderson D, Ho SY, Houyel L et al (2016) Congenital coronary artery anomalies: a bridge from embryology to anatomy and pathophysiology—a position statement of the development, anatomy, and pathology ESC Working Group. Cardiovasc Res 109(2):204–216 CrossRefPubMed
25.
go back to reference Bulkley BH, D’Amico B, Taylor AL (1983) Extensive myocardial fiber disarray in aortic and pulmonary atresia. Relevance to hypertrophic cardiomyopathy. Circulation 67(1):191–198 CrossRefPubMed Bulkley BH, D’Amico B, Taylor AL (1983) Extensive myocardial fiber disarray in aortic and pulmonary atresia. Relevance to hypertrophic cardiomyopathy. Circulation 67(1):191–198 CrossRefPubMed
26.
go back to reference Sakurai H, Sakurai T, Ohashi N, Nishikawa H (2018) Aortic to right ventricular shunt for pulmonary atresia with intact ventricular septum and bilateral coronary ostial atresia. J Thorac Cardiovasc Surg 156(1):e17-20 CrossRefPubMed Sakurai H, Sakurai T, Ohashi N, Nishikawa H (2018) Aortic to right ventricular shunt for pulmonary atresia with intact ventricular septum and bilateral coronary ostial atresia. J Thorac Cardiovasc Surg 156(1):e17-20 CrossRefPubMed
27.
go back to reference Wald RM, Juraszek AL, Pigula FA, Geva T (2006) Echocardiographic diagnosis and management of bilateral coronary ostial atresia in a patient with pulmonary atresia and intact ventricular septum. J Am Soc Echocardiogr 19(7):939.e1-939.e3 CrossRefPubMed Wald RM, Juraszek AL, Pigula FA, Geva T (2006) Echocardiographic diagnosis and management of bilateral coronary ostial atresia in a patient with pulmonary atresia and intact ventricular septum. J Am Soc Echocardiogr 19(7):939.e1-939.e3 CrossRefPubMed
Metadata
Title
Aorta Without Coronary Arteries: Anatomic Variants of a Rare Malformation
Authors
Julie Karila-Cohen
Daniela Laux
Lucile Houyel
Damien Bonnet
Publication date
07-11-2023