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Erschienen in: Pediatric Cardiology 1/2024

07.11.2023 | Case Report

Aorta Without Coronary Arteries: Anatomic Variants of a Rare Malformation

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

Erschienen in: Pediatric Cardiology | Ausgabe 1/2024

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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.
Literatur
1.
Zurück zum Zitat 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):511–514CrossRefPubMed 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):511–514CrossRefPubMed
2.
Zurück zum Zitat 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):348–350PubMedPubMedCentral 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):348–350PubMedPubMedCentral
3.
Zurück zum Zitat 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):706–708CrossRefPubMed 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):706–708CrossRefPubMed
4.
Zurück zum Zitat Legendre A, Houyel L, Serraf A (2006) Severe anomaly of coronary-artery development. N Engl J Med 355(6):631–633CrossRefPubMed Legendre A, Houyel L, Serraf A (2006) Severe anomaly of coronary-artery development. N Engl J Med 355(6):631–633CrossRefPubMed
5.
Zurück zum Zitat 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):437–441CrossRef 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):437–441CrossRef
6.
Zurück zum Zitat 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):1198–1205CrossRefPubMed 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):1198–1205CrossRefPubMed
7.
Zurück zum Zitat 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):487–489CrossRef 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):487–489CrossRef
8.
Zurück zum Zitat 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):294–296CrossRefPubMed 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):294–296CrossRefPubMed
9.
Zurück zum Zitat 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–W45CrossRefPubMed 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–W45CrossRefPubMed
10.
Zurück zum Zitat 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):836–838CrossRefPubMed 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):836–838CrossRefPubMed
11.
Zurück zum Zitat 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):246–249CrossRef 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):246–249CrossRef
12.
Zurück zum Zitat 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):108–110CrossRefPubMed 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):108–110CrossRefPubMed
13.
Zurück zum Zitat 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–e196CrossRefPubMed 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–e196CrossRefPubMed
14.
Zurück zum Zitat 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):162–165PubMedPubMedCentral 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):162–165PubMedPubMedCentral
15.
Zurück zum Zitat Sharma B, Chang A, Red-Horse K (2017) Coronary artery development: progenitor cells and differentiation pathways. Annu Rev Physiol 79(1):1–19CrossRefPubMed Sharma B, Chang A, Red-Horse K (2017) Coronary artery development: progenitor cells and differentiation pathways. Annu Rev Physiol 79(1):1–19CrossRefPubMed
16.
Zurück zum Zitat Tomanek R, Angelini P (2019) Embryology of coronary arteries and anatomy/pathophysiology of coronary anomalies. A comprehensive update. Int J Cardiol 281:28–34CrossRefPubMed Tomanek R, Angelini P (2019) Embryology of coronary arteries and anatomy/pathophysiology of coronary anomalies. A comprehensive update. Int J Cardiol 281:28–34CrossRefPubMed
17.
Zurück zum Zitat Red-Horse K, Ueno H, Weissman IL, Krasnow MA (2010) Coronary arteries form by developmental reprogramming of venous cells. Nature 464(7288):549–553CrossRefPubMedPubMedCentral Red-Horse K, Ueno H, Weissman IL, Krasnow MA (2010) Coronary arteries form by developmental reprogramming of venous cells. Nature 464(7288):549–553CrossRefPubMedPubMedCentral
18.
Zurück zum Zitat 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):656–661CrossRefPubMedPubMedCentral 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):656–661CrossRefPubMedPubMedCentral
19.
Zurück zum Zitat 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):4899–4914CrossRefPubMedPubMedCentral 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):4899–4914CrossRefPubMedPubMedCentral
20.
Zurück zum Zitat 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):455–468CrossRefPubMedPubMedCentral 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):455–468CrossRefPubMedPubMedCentral
21.
22.
Zurück zum Zitat 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):43–57CrossRef 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):43–57CrossRef
23.
Zurück zum Zitat 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):445–459CrossRefPubMed 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):445–459CrossRefPubMed
24.
Zurück zum Zitat 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):204–216CrossRefPubMed 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):204–216CrossRefPubMed
25.
Zurück zum Zitat Bulkley BH, D’Amico B, Taylor AL (1983) Extensive myocardial fiber disarray in aortic and pulmonary atresia. Relevance to hypertrophic cardiomyopathy. Circulation 67(1):191–198CrossRefPubMed Bulkley BH, D’Amico B, Taylor AL (1983) Extensive myocardial fiber disarray in aortic and pulmonary atresia. Relevance to hypertrophic cardiomyopathy. Circulation 67(1):191–198CrossRefPubMed
26.
Zurück zum Zitat 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):e17-20CrossRefPubMed 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):e17-20CrossRefPubMed
27.
Zurück zum Zitat 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.e3CrossRefPubMed 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.e3CrossRefPubMed
Metadaten
Titel
Aorta Without Coronary Arteries: Anatomic Variants of a Rare Malformation
verfasst von
Julie Karila-Cohen
Daniela Laux
Lucile Houyel
Damien Bonnet
Publikationsdatum
07.11.2023
Verlag
Springer US
Erschienen in
Pediatric Cardiology / Ausgabe 1/2024
Print ISSN: 0172-0643
Elektronische ISSN: 1432-1971
DOI
https://doi.org/10.1007/s00246-023-03330-7

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