Total anomalous pulmonary venous connection is usually seen and treated in childhood or in neonatal period in his obstructive type. Sometime it can be detected beyond the first decade. The objective of this case report is to give prove of the fact that it can be seen and treated in a teenager. We present a rare case of 15 years old boy who was admitted for supraventricular tachycardia with hypotension. Emergency electrocardiography showed atrial Flutter with a frequency of 225 beats/min. He complained from dyspnea state 2 at New York Heart Association functional classification before. The echocardiography showed a dilated coronary sinus in cardiac-type total anomalous pulmonary venous connection associated with a large atrial septal defect. Cardiac rhythm was normal after administration of Amiodarone. In cardiopulmonary bypass, an incision was made from the atrial septal defect to unroof the coronary sinus; a large pericardial patch was put to close the unroofing coronary sinus and let it in the left atrium. A De Vega tricuspid annuloplasty was done to reduce the tricuspid valve leak. The patient’s postoperative course was uneventful and was discharged in day 9 after operation. Total pulmonary venous return can evolve until teenage if the atrial septal defect is large. Evolution is good after a complete repair.
| Published in | International Journal of Cardiovascular and Thoracic Surgery (Volume 5, Issue 4) |
| DOI | 10.11648/j.ijcts.20190504.12 |
| Page(s) | 69-71 |
| 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), 2019. Published by Science Publishing Group |
Atrial Septal Defect, Coronary Sinus, Total Anomalous Pulmonary Venous Connection, Unroofing Coronary Sinus, Pericardial Patch
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APA Style
Papa Salmane Ba, Momar Sokhna Diop, Papa Amath Diagne, Ndeye Fatou Sow, Papa Adama Dieng, et al. (2019). Total Anomalous Pulmonary Venous Connection in a Teenage Patient. International Journal of Cardiovascular and Thoracic Surgery, 5(4), 69-71. https://doi.org/10.11648/j.ijcts.20190504.12
ACS Style
Papa Salmane Ba; Momar Sokhna Diop; Papa Amath Diagne; Ndeye Fatou Sow; Papa Adama Dieng, et al. Total Anomalous Pulmonary Venous Connection in a Teenage Patient. Int. J. Cardiovasc. Thorac. Surg. 2019, 5(4), 69-71. doi: 10.11648/j.ijcts.20190504.12
AMA Style
Papa Salmane Ba, Momar Sokhna Diop, Papa Amath Diagne, Ndeye Fatou Sow, Papa Adama Dieng, et al. Total Anomalous Pulmonary Venous Connection in a Teenage Patient. Int J Cardiovasc Thorac Surg. 2019;5(4):69-71. doi: 10.11648/j.ijcts.20190504.12
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Download@article{10.11648/j.ijcts.20190504.12,
author = {Papa Salmane Ba and Momar Sokhna Diop and Papa Amath Diagne and Ndeye Fatou Sow and Papa Adama Dieng and Amadou Gabriel Ciss and Mouhamadou N’Diaye},
title = {Total Anomalous Pulmonary Venous Connection in a Teenage Patient},
journal = {International Journal of Cardiovascular and Thoracic Surgery},
volume = {5},
number = {4},
pages = {69-71},
doi = {10.11648/j.ijcts.20190504.12},
url = {https://doi.org/10.11648/j.ijcts.20190504.12},
eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ijcts.20190504.12},
abstract = {Total anomalous pulmonary venous connection is usually seen and treated in childhood or in neonatal period in his obstructive type. Sometime it can be detected beyond the first decade. The objective of this case report is to give prove of the fact that it can be seen and treated in a teenager. We present a rare case of 15 years old boy who was admitted for supraventricular tachycardia with hypotension. Emergency electrocardiography showed atrial Flutter with a frequency of 225 beats/min. He complained from dyspnea state 2 at New York Heart Association functional classification before. The echocardiography showed a dilated coronary sinus in cardiac-type total anomalous pulmonary venous connection associated with a large atrial septal defect. Cardiac rhythm was normal after administration of Amiodarone. In cardiopulmonary bypass, an incision was made from the atrial septal defect to unroof the coronary sinus; a large pericardial patch was put to close the unroofing coronary sinus and let it in the left atrium. A De Vega tricuspid annuloplasty was done to reduce the tricuspid valve leak. The patient’s postoperative course was uneventful and was discharged in day 9 after operation. Total pulmonary venous return can evolve until teenage if the atrial septal defect is large. Evolution is good after a complete repair.},
year = {2019}
}
TY - JOUR T1 - Total Anomalous Pulmonary Venous Connection in a Teenage Patient AU - Papa Salmane Ba AU - Momar Sokhna Diop AU - Papa Amath Diagne AU - Ndeye Fatou Sow AU - Papa Adama Dieng AU - Amadou Gabriel Ciss AU - Mouhamadou N’Diaye Y1 - 2019/10/09 PY - 2019 N1 - https://doi.org/10.11648/j.ijcts.20190504.12 DO - 10.11648/j.ijcts.20190504.12 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 - 69 EP - 71 PB - Science Publishing Group SN - 2575-4882 UR - https://doi.org/10.11648/j.ijcts.20190504.12 AB - Total anomalous pulmonary venous connection is usually seen and treated in childhood or in neonatal period in his obstructive type. Sometime it can be detected beyond the first decade. The objective of this case report is to give prove of the fact that it can be seen and treated in a teenager. We present a rare case of 15 years old boy who was admitted for supraventricular tachycardia with hypotension. Emergency electrocardiography showed atrial Flutter with a frequency of 225 beats/min. He complained from dyspnea state 2 at New York Heart Association functional classification before. The echocardiography showed a dilated coronary sinus in cardiac-type total anomalous pulmonary venous connection associated with a large atrial septal defect. Cardiac rhythm was normal after administration of Amiodarone. In cardiopulmonary bypass, an incision was made from the atrial septal defect to unroof the coronary sinus; a large pericardial patch was put to close the unroofing coronary sinus and let it in the left atrium. A De Vega tricuspid annuloplasty was done to reduce the tricuspid valve leak. The patient’s postoperative course was uneventful and was discharged in day 9 after operation. Total pulmonary venous return can evolve until teenage if the atrial septal defect is large. Evolution is good after a complete repair. VL - 5 IS - 4 ER -
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