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Updated: Jan 26, 2026

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Published on: November 18, 2018
Partial anomalous pulmonary venous return: A case series with management approach
Karim El-Kersh1, Elie Homsy2, Curt J Daniels3,4
1Department of Internal Medicine, Division of Pulmonary, Critical Care and Sleep Disorders Medicine, University of Louisville, Louisville, KY, USA.
Partial anomalous pulmonary venous return (PAPVR) can lead to pulmonary arterial hypertension and Eisenmenger's syndrome if unrepaired. This study highlights varied PAPVR presentations and tailored treatments, including observation, surgery, and vasodilator therapies.
Area of Science:
- Cardiology
- Congenital Heart Disease
- Pulmonology
Background:
- Partial anomalous pulmonary venous return (PAPVR) is a rare congenital heart defect characterized by abnormal pulmonary venous connection.
- It leads to a left-to-right shunt, with clinical presentation varying based on shunt volume.
Observation:
- Unrepaired significant shunts can cause pulmonary vascular remodeling and pulmonary arterial hypertension (PAH).
- Co-occurrence with atrial septal defects (ASD) may precipitate shunt reversal and Eisenmenger's syndrome in severe PAH cases.
Findings:
- This study presents diverse clinical cases of PAPVR.
- Individualized management strategies are crucial for optimal outcomes.
Implications:
- Early recognition and management of PAPVR are vital to prevent progression to PAH and Eisenmenger's syndrome.
- Treatment approaches, including observation, surgical correction, and pharmacotherapy, should be tailored to each patient's specific presentation and shunt severity.
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