Anomalous origin of one pulmonary artery from aorta: Evaluation on computed tomography angiography
Mansi Verma1, Niraj Nirmal Pandey1, Sivasubramanian Ramakrishnan2
1Department of Cardiovascular Radiology and Endovascular Interventions, All India Institute of Medical Sciences, New Delhi, India.
Insights
Anomalous origin of pulmonary artery from aorta (AOPA) is rare and often linked to other heart defects. CT angiography is crucial for precise diagnosis and surgical planning in these complex cases.
Area of Science:
- Cardiovascular Imaging and Diagnostics
- Pediatric Cardiology
- Congenital Heart Disease
Background:
- Anomalous origin of the pulmonary artery from aorta (AOPA) is a rare congenital heart defect.
- It necessitates detailed anatomical assessment due to frequent associations with other cardiovascular anomalies.
Purpose of the Study:
- To evaluate the morphological characteristics of AOPA.
- To identify associated cardiovascular anomalies in patients with AOPA using CT angiography.
Main Methods:
- Retrospective analysis of CT angiography data from January 2014 to September 2021.
- Inclusion of patients diagnosed with AOPA.
- Assessment of AOPA subtype, origin, and coexisting cardiac abnormalities.
Main Results:
- AOPA was identified in 27 patients, with anomalous origin of the right pulmonary artery (AORPA) in 63% and anomalous origin of the left pulmonary artery (AOLPA) in 37%.
- The proximal subtype of AOPA was more common (88.9%).
- AOPA was associated with other cardiac anomalies in 92.6% of patients, including patent arterial duct (with AORPA) and tetralogy of Fallot (with AOLPA). Right-sided aortic arch was observed in 80% of AOLPA cases.
Conclusions:
- AOPA is a rare condition frequently accompanied by significant cardiovascular anomalies.
- CT angiography provides essential anatomical detail for surgical planning.
- Early and accurate diagnosis aids in managing patients with AOPA and associated defects.
Aim:
The present study sought to evaluate the morphology and associated cardiovascular anomalies in patients with anomalous origin of one pulmonary artery from aorta (AOPA) on CT angiography.
Materials And Methods:
A retrospective search of the departmental database from January 2014 to September 2021 was conducted to identify patients diagnosed with AOPA on CT angiography. The subtype of AOPA, site of origin, and associated cardiovascular abnormalities were assessed.
Results:
AOPA was identified in 27 patients (19 males, mean age: 8.8 years). Anomalous origin of the right pulmonary artery from aorta (AORPA) was observed in 17/27 (63%) patients, while anomalous origin of the left pulmonary artery (AOLPA) was seen in 10/27 (37%) patients. The proximal and distal subtypes were observed in 24/27 (88.9%) and 3/27 (11.1%) patients respectively. AOPA was associated with other cardiac anomalies in 92.6% (25/27) patients. Patent arterial duct (11/17; 64.7%) was the most frequently anomaly associated with AORPA, while tetralogy of Fallot (10/10; 100%) was the most commonly anomaly associated with AOLPA. The anomalous pulmonary artery was contralateral to the aortic arch in 23/27 (85.2%) patients. Right-sided aortic arch was observed in only 2/17 (11.8%) patients with AORPA and 8/10 (80%) patients with AOLPA. In 2/10 (20%) patients, AORPA was associated with aortopulmonary window and aortic arch anomaly.
Conclusion:
AOPA is rare and frequently associated with other cardiovascular anomalies like patent arterial duct, tetralogy of Fallot, and right-sided aortic arch. CT angiography helps in providing exact anatomical delineation and identifying associated anomalies, thus aiding preoperative planning of surgical management.
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