جمعه 8 فروردین 1404
دوره 8، شماره 2 - ( 1-1399 )
جلد 8 شماره 2 صفحات 132-127 |
برگشت به فهرست نسخه ها
Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
Ghaemi H R, Zamani H, Babazadeh K, Navaeifar M R. Anomalous Origin of Left Coronary Artery From Pulmonary Artery: A Case Series and Review of Literature. J. Pediatr. Rev 2020; 8 (2) :127-132
URL: http://jpr.mazums.ac.ir/article-1-246-fa.html
URL: http://jpr.mazums.ac.ir/article-1-246-fa.html
Anomalous Origin of Left Coronary Artery From Pulmonary Artery: A Case Series and Review of Literature. Journal of Pediatrics Review. 1399; 8 (2) :127-132
چکیده: (5134 مشاهده)
Introduction: Anomalous left coronary artery from the pulmonary artery (ALCAPA) is a rare cardiovascular disease presented with an incidence of 1 per 300000 live births.
Case Presentation: In this article, we present four cases of ALCAPA in infancy. Two infants presented with respiratory distress and two with a heart murmur. Their coronary arteries were derived from their pulmonary arteries. Two of them died, one after surgical procedure and one before surgical intervention. Of remained cases, one of them had a good surgical outcome, and another was missed in the follow-up.
A brief review was done on case reports of ALCAPA in children. Eighteen articles were found, including 201 pediatric cases.
Conclusions: The vast majority of affected children will die within the first year of life if ALCAPA is not diagnosed and treated appropriately.
Case Presentation: In this article, we present four cases of ALCAPA in infancy. Two infants presented with respiratory distress and two with a heart murmur. Their coronary arteries were derived from their pulmonary arteries. Two of them died, one after surgical procedure and one before surgical intervention. Of remained cases, one of them had a good surgical outcome, and another was missed in the follow-up.
A brief review was done on case reports of ALCAPA in children. Eighteen articles were found, including 201 pediatric cases.
Conclusions: The vast majority of affected children will die within the first year of life if ALCAPA is not diagnosed and treated appropriately.
نوع مطالعه: Case Report and Review of Literature |
دریافت: 1398/3/26 | پذیرش: 1398/6/16 | انتشار: 1399/1/13
دریافت: 1398/3/26 | پذیرش: 1398/6/16 | انتشار: 1399/1/13
| بازنشر اطلاعات | |
 |
این مقاله تحت شرایط Creative Commons Attribution-NonCommercial 4.0 International License قابل بازنشر است. |
