2020
DOI: 10.1111/jocs.15238
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Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) in adults: Collateral circulation does not preclude direct reimplantation

Abstract: Background: The adult type of anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is characterized by late presentation due to collateral coronary flow. Patients often present with long time recurrent angina or dyspnea. Surgical correction can be a challenge due to the vast collateral coronary circulation. Case presentation: A previously healthy 41-year-old male presented in the emergency room referring typical angina and dyspnea. Coronary angiography revealed ALCAPA. Surgical corre… Show more

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Cited by 7 publications
(7 citation statements)
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“…In this study, no significant differences in the recovery of ventricular function existed among the three groups. After ALCAPA repair, the left ventricular function of most patients returned to normal regardless of concomitant mitral valve intervention, which is similar to that reported in most literature ( 19 21 ). In addition, we found that the left ventricular diameter of most patients improved significantly before discharge, and the LVEF did not improve immediately.…”
Section: Discussionsupporting
confidence: 87%
“…In this study, no significant differences in the recovery of ventricular function existed among the three groups. After ALCAPA repair, the left ventricular function of most patients returned to normal regardless of concomitant mitral valve intervention, which is similar to that reported in most literature ( 19 21 ). In addition, we found that the left ventricular diameter of most patients improved significantly before discharge, and the LVEF did not improve immediately.…”
Section: Discussionsupporting
confidence: 87%
“…ALCAPA classically presents with symptoms of heart failure secondary to ischemia in an extensive myocardial territory (5,6). The age of presentation depends on the number and quality of collaterals from the right coronary system to meet myocardial demands (7).…”
Section: Discussionmentioning
confidence: 99%
“…The arising of the left common coronary artery (LCCA) from the PA (ALCAPA), known as Bland-White-Garland syndrome, was first described in 1933 [5][6][7]. This disease represents 0.24-0.46% of all congenital heart malformations, which represents an incidence of 1 in 300,000 [1,4,[8][9][10].…”
Section: Introductionmentioning
confidence: 99%
“…The incidence of anomalous origin of the right coronary artery (RCA) from the pulmonary artery (PA) (ARCAPA) is 1 in 500,000 and was first described in 1882 by John Brook [1]. It represents 0.12% of all congenital heart diseases [1][2][3][4][5][6][7][8][9][10][11][12][13][14]. The lower incidence of ARCAPA in comparison with ALCAPA is caused by the higher intimacy of the left common coronary artery (LCCA) origin to the PA sinus [6].…”
Section: Introductionmentioning
confidence: 99%