The Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA) in Senegal

Mohamed Leye; Fatou Aw; Adama Sawadogo; Maria Helena Diame; Momar Dioum; Désiré Alain Affangla; Simon Manga; Abdoulaye Ndoye Diop; Bassirou Bah; Magalie Kaya Samba; Alassane Aliou Ngaide; Alassane Mbaye; Modibo Doumbia; Djibril Marie Ba; Rosette Godonou; Abdoul Kane

doi:doi:10.11648/j.ijcts.20170302.12

The Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA) in Senegal

Mohamed Leye, Fatou Aw, Adama Sawadogo, Maria Helena Diame, Momar Dioum, Désiré Alain Affangla, Simon Manga, Abdoulaye Ndoye Diop, Bassirou Bah, Magalie Kaya Samba, Alassane Aliou Ngaide, Alassane Mbaye, Modibo Doumbia, Djibril Marie Ba, Rosette Godonou, Abdoul Kane

Published in International Journal of Cardiovascular and Thoracic Surgery (Volume 3, Issue 2)

Received: 21 May 2017 Accepted: 19 June 2017 Published: 25 July 2017

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Abstract

The anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare malformation that represents less than 0.5% of the congenital heart diseases. The common clinical feature is congestive heart failure. The treatment is strictly a surgical repair. The authors report the first 3 cases of ALCAPA diagnosed in Senegal in infants under the age of 1 year old. Two were successfully treated by surgical repair; the 3^rd child is still waiting for surgical repair to be performed abroad.

Published in	International Journal of Cardiovascular and Thoracic Surgery (Volume 3, Issue 2)
DOI	10.11648/j.ijcts.20170302.12
Page(s)	9-13
Creative Commons	This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.
Copyright	Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

ALCAPA, Africa, Dilated Cardiomyopathy, Coronary Artery Re-implantation, Infant, Ischemic Heart

References

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[2]	Keith JD. The anomalous origin of the left coronary artery from the pulmonary artery. Brit Heart J. 1959, 21:149-61.
[3]	Kumar RV, Krishna LSR, Ramachandran G. Anomalous origin of the left coronary artery arising from the pulmonary artery: Reverse remodeling of coronary arteries following translocation operation. Indian J Thorac Cardiovasc Surg 2012; 28 (2):151–2.
[4]	Levin SE, Dansky R, Kinsley RH. Origin of left coronary artery from right pulmonary artery co-existing with coarctation of the aorta. Int J Cardiol 1990; 27:31-6.
[5]	Michielon G, Di Carlo D, Brancaccio G. et al. Anomalous coronary artery origin from the pulmonary artery: correlation between surgical timing and left ventricular function recovering. Ann Thor Surg 2003; 76:581-8.
[6]	Nakle N, Biscardi S, Lambert V, Sigal-Cinqualbre A, Epaud R, Madhi F. Anomalie de naissance de la coronaire gauche à partir de l’artère pulmonaire révélée par une Bronchiolite. Rev Mal Resp 2012; 29: 912-15.
[7]	Pena E, Nguyen TE, Merchant N, Dennie C. ALCAPA Syndrome: not just a pediatric disease. RadioGraphics 2009; 29:553–65.
[8]	Shivalkar B, Borgers M, Daenen W, et al. ALCAPA syndrome: an example of chronic myocardial hypoperfusion? J Am Coll Cardiol 1994; 23:772-8.
[9]	Toumpourleka M, Belitsis G, Alonso R, Rubens M, Moat N, Gatzoulis M. Late presentation and surgical repair of ALCAPA. Int J Cardiol 2015; 186:207-209.
[10]	Toussaint M, Goube P, Kuoch V, Defrance C, Amrar-Venier F, Nicollet E, Gonin S, Busy F, Lardoux H. Origine anormale de la coronaire ga uche à partir de l’artère pulmonaire: place du scanner 64 coupes. J Radiol 2011; 92:1124-7.
[11]	Trabelsi Sahnoun I, Abid L, Abid D, Triki F, Sahnoun M, Krichene S, Hentati M, Kammoun S. la naissance anormale du tronc coronaire gauche à partir de l’artere pulmonaire : etiologie de defaillance cardiaque chez le nourrisson. J. I. M. Sfax 2008; 15 (16):23 – 5.
[12]	Uysal F, Bostan OM, Semizel E, Signak IS, Asut E, Cil E. Congenital anomalies of coronary arteries in children:the evaluation of 22 patients. Pediatr Cardiol 2013;
[13]	Wang S S, Chen X X, M D, Chen J M, Zhang Z W, MaY, Huang M P, Zhuang J. Echocardiographic findings of an anomalous origin of the left coronary artery in children and adolescents. Real or fake? J Ultrasound Med 2016; 35:59–66.

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APA Style

Mohamed Leye, Fatou Aw, Adama Sawadogo, Maria Helena Diame, Momar Dioum, et al. (2017). The Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA) in Senegal. International Journal of Cardiovascular and Thoracic Surgery, 3(2), 9-13. https://doi.org/10.11648/j.ijcts.20170302.12

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ACS Style

Mohamed Leye; Fatou Aw; Adama Sawadogo; Maria Helena Diame; Momar Dioum, et al. The Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA) in Senegal. Int. J. Cardiovasc. Thorac. Surg. 2017, 3(2), 9-13. doi: 10.11648/j.ijcts.20170302.12

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AMA Style

Mohamed Leye, Fatou Aw, Adama Sawadogo, Maria Helena Diame, Momar Dioum, et al. The Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA) in Senegal. Int J Cardiovasc Thorac Surg. 2017;3(2):9-13. doi: 10.11648/j.ijcts.20170302.12

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@article{10.11648/j.ijcts.20170302.12,
  author = {Mohamed Leye and Fatou Aw and Adama Sawadogo and Maria Helena Diame and Momar Dioum and Désiré Alain Affangla and Simon Manga and Abdoulaye Ndoye Diop and Bassirou Bah and Magalie Kaya Samba and Alassane Aliou Ngaide and Alassane Mbaye and Modibo Doumbia and Djibril Marie Ba and Rosette Godonou and Abdoul Kane},
  title = {The Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA) in Senegal},
  journal = {International Journal of Cardiovascular and Thoracic Surgery},
  volume = {3},
  number = {2},
  pages = {9-13},
  doi = {10.11648/j.ijcts.20170302.12},
  url = {https://doi.org/10.11648/j.ijcts.20170302.12},
  eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ijcts.20170302.12},
  abstract = {The anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare malformation that represents less than 0.5% of the congenital heart diseases. The common clinical feature is congestive heart failure. The treatment is strictly a surgical repair. The authors report the first 3 cases of ALCAPA diagnosed in Senegal in infants under the age of 1 year old. Two were successfully treated by surgical repair; the 3rd child is still waiting for surgical repair to be performed abroad.},
 year = {2017}
}

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TY  - JOUR
T1  - The Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA) in Senegal
AU  - Mohamed Leye
AU  - Fatou Aw
AU  - Adama Sawadogo
AU  - Maria Helena Diame
AU  - Momar Dioum
AU  - Désiré Alain Affangla
AU  - Simon Manga
AU  - Abdoulaye Ndoye Diop
AU  - Bassirou Bah
AU  - Magalie Kaya Samba
AU  - Alassane Aliou Ngaide
AU  - Alassane Mbaye
AU  - Modibo Doumbia
AU  - Djibril Marie Ba
AU  - Rosette Godonou
AU  - Abdoul Kane
Y1  - 2017/07/25
PY  - 2017
N1  - https://doi.org/10.11648/j.ijcts.20170302.12
DO  - 10.11648/j.ijcts.20170302.12
T2  - International Journal of Cardiovascular and Thoracic Surgery
JF  - International Journal of Cardiovascular and Thoracic Surgery
JO  - International Journal of Cardiovascular and Thoracic Surgery
SP  - 9
EP  - 13
PB  - Science Publishing Group
SN  - 2575-4882
UR  - https://doi.org/10.11648/j.ijcts.20170302.12
AB  - The anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare malformation that represents less than 0.5% of the congenital heart diseases. The common clinical feature is congestive heart failure. The treatment is strictly a surgical repair. The authors report the first 3 cases of ALCAPA diagnosed in Senegal in infants under the age of 1 year old. Two were successfully treated by surgical repair; the 3rd child is still waiting for surgical repair to be performed abroad.
VL  - 3
IS  - 2
ER  -

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Author Information

Mohamed Leye

Unit of Training and Research in Medical Sciences, University of Thies, Thies, Senegal
Fatou Aw

Department of Cardiology, Cheikh Anta Diop University, Dakar, Senegal
Adama Sawadogo

Department of Cardiovascular and Thoracic Surgery, Cheikh Anta Diop University, Dakar, Senegal
Maria Helena Diame

Unit of Training and Research in Medical Sciences, University of Thies, Thies, Senegal
Momar Dioum

Department of Cardiology, Cheikh Anta Diop University, Dakar, Senegal
Désiré Alain Affangla

Unit of Training and Research in Medical Sciences, University of Thies, Thies, Senegal
Simon Manga

Department of Cardiology, University of Ziguinchor, Ziguinchor, Senagal
Abdoulaye Ndoye Diop

Department of Radiology, University of Saint Louis, Saint Louis, Senegal
Bassirou Bah

Unit of Training and Research in Medical Sciences, University of Thies, Thies, Senegal
Magalie Kaya Samba

Department of Cardiology, Cheikh Anta Diop University, Dakar, Senegal
Alassane Aliou Ngaide

Department of Cardiology, Cheikh Anta Diop University, Dakar, Senegal
Alassane Mbaye

Department of Cardiology, Cheikh Anta Diop University, Dakar, Senegal
Modibo Doumbia

Department of Cardiovascular and Thoracic Surgery, Cheikh Anta Diop University, Dakar, Senegal
Djibril Marie Ba

Unit of Training and Research in Medical Sciences, University of Thies, Thies, Senegal
Rosette Godonou

Unit of Training and Research in Medical Sciences, University of Thies, Thies, Senegal
Abdoul Kane

Department of Cardiology, Cheikh Anta Diop University, Dakar, Senegal

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Plain Text BibTeX RIS

APA Style

Mohamed Leye, Fatou Aw, Adama Sawadogo, Maria Helena Diame, Momar Dioum, et al. (2017). The Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA) in Senegal. International Journal of Cardiovascular and Thoracic Surgery, 3(2), 9-13. https://doi.org/10.11648/j.ijcts.20170302.12

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ACS Style

Mohamed Leye; Fatou Aw; Adama Sawadogo; Maria Helena Diame; Momar Dioum, et al. The Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA) in Senegal. Int. J. Cardiovasc. Thorac. Surg. 2017, 3(2), 9-13. doi: 10.11648/j.ijcts.20170302.12

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AMA Style

Mohamed Leye, Fatou Aw, Adama Sawadogo, Maria Helena Diame, Momar Dioum, et al. The Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA) in Senegal. Int J Cardiovasc Thorac Surg. 2017;3(2):9-13. doi: 10.11648/j.ijcts.20170302.12

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@article{10.11648/j.ijcts.20170302.12,
  author = {Mohamed Leye and Fatou Aw and Adama Sawadogo and Maria Helena Diame and Momar Dioum and Désiré Alain Affangla and Simon Manga and Abdoulaye Ndoye Diop and Bassirou Bah and Magalie Kaya Samba and Alassane Aliou Ngaide and Alassane Mbaye and Modibo Doumbia and Djibril Marie Ba and Rosette Godonou and Abdoul Kane},
  title = {The Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA) in Senegal},
  journal = {International Journal of Cardiovascular and Thoracic Surgery},
  volume = {3},
  number = {2},
  pages = {9-13},
  doi = {10.11648/j.ijcts.20170302.12},
  url = {https://doi.org/10.11648/j.ijcts.20170302.12},
  eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ijcts.20170302.12},
  abstract = {The anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare malformation that represents less than 0.5% of the congenital heart diseases. The common clinical feature is congestive heart failure. The treatment is strictly a surgical repair. The authors report the first 3 cases of ALCAPA diagnosed in Senegal in infants under the age of 1 year old. Two were successfully treated by surgical repair; the 3rd child is still waiting for surgical repair to be performed abroad.},
 year = {2017}
}

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TY  - JOUR
T1  - The Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA) in Senegal
AU  - Mohamed Leye
AU  - Fatou Aw
AU  - Adama Sawadogo
AU  - Maria Helena Diame
AU  - Momar Dioum
AU  - Désiré Alain Affangla
AU  - Simon Manga
AU  - Abdoulaye Ndoye Diop
AU  - Bassirou Bah
AU  - Magalie Kaya Samba
AU  - Alassane Aliou Ngaide
AU  - Alassane Mbaye
AU  - Modibo Doumbia
AU  - Djibril Marie Ba
AU  - Rosette Godonou
AU  - Abdoul Kane
Y1  - 2017/07/25
PY  - 2017
N1  - https://doi.org/10.11648/j.ijcts.20170302.12
DO  - 10.11648/j.ijcts.20170302.12
T2  - International Journal of Cardiovascular and Thoracic Surgery
JF  - International Journal of Cardiovascular and Thoracic Surgery
JO  - International Journal of Cardiovascular and Thoracic Surgery
SP  - 9
EP  - 13
PB  - Science Publishing Group
SN  - 2575-4882
UR  - https://doi.org/10.11648/j.ijcts.20170302.12
AB  - The anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare malformation that represents less than 0.5% of the congenital heart diseases. The common clinical feature is congestive heart failure. The treatment is strictly a surgical repair. The authors report the first 3 cases of ALCAPA diagnosed in Senegal in infants under the age of 1 year old. Two were successfully treated by surgical repair; the 3rd child is still waiting for surgical repair to be performed abroad.
VL  - 3
IS  - 2
ER  -

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