Patent ductus arteriosus associated with congenital anomaly of coronary artery
Majid Maleki1, Nassrin Azizian1, Maryam Esmaeilzadeh1
1Echocardiography Research Center, Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, IR Iran.
Insights
This case report details a patient with patent ductus arteriosus (PDA) and anomalous coronary arteries. Surgical closure of the PDA was successful, resolving symptoms.
Area of Science:
- Cardiology
- Congenital Heart Disease
- Cardiac Surgery
Background:
- Patent ductus arteriosus (PDA) is a common congenital heart defect.
- Congenital anomalies of the coronary arteries, such as anomalous origin, can present with varied clinical manifestations.
- The coexistence of PDA and coronary anomalies requires careful diagnostic evaluation.
Observation:
- A 21-year-old male presented with a cardiac murmur, palpitations, and atypical chest pain.
- Physical examination revealed a continuous murmur.
- Transthoracic echocardiography demonstrated a PDA with dilated pulmonary arteries and normal ventricular function, alongside an abnormal origin of both right and left coronary arteries from a single ostium.
Findings:
- The patient had a patent ductus arteriosus (PDA) combined with a rare congenital anomaly: the abnormal origin of both the right coronary artery (RCA) and left coronary artery (LCA) from a single ostium in the right coronary sinus.
- Despite the coronary anomaly, there was evidence of normal coronary flow and no clinical signs of myocardial ischemia.
- Surgical closure of the PDA was performed successfully.
Implications:
- This case highlights the importance of comprehensive cardiac evaluation in patients presenting with PDA, especially when accompanied by atypical symptoms.
- The successful surgical management of PDA in the presence of coronary anomalies underscores the feasibility of intervention even in complex congenital heart disease.
- Further research into the long-term outcomes and management strategies for combined PDA and coronary artery anomalies is warranted.
Abstract:
We reported a case of patent ductus arteriosus (PDA) with congenital anomaly of coronary arteries as abnormal origin of right coronary artery (RCA) and left coronary artery (LCA) from a single ostium of the right coronary sinus. A 21-year-old man referred to our institution for evaluation of cardiac murmur. He has suffered from palpitation and atypical chest pain for three months. On physical examination, a continuous murmur was heard in the second left parasternal space. Transthoracic echocardiography showed normal left and right ventricular size and systolic function (LVEF = 55%). Main pulmonary artery (PA) and left pulmonary artery (LPA) branch were considerably dilated. Considering normal coronary flow, lack of clinical evidence of myocardial ischemia and echocardiography findings, patient underwent surgical closure of PDA via left thoracotomy and after five days discharged uneventfully.
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