Pulmonary Agenesis and Persistent Left Superior Vena Cava with Aberrant Drainage
▶ Watch on YouTube — age-restricted, cannot embed here
Imaging findings
Unilateral pulmonary agenesis (absent left pulmonary artery, with the left lung supplied by bronchial collaterals) in a patient with repaired congenital heart disease (RV to conduit, VSD patch repair). A persistent left superior vena cava (PLSVC) was observed with an abnormal course, descending lateral to the aortic arch, then coursing medially to drain into the right atrium, rather than into the coronary sinus or anterior to the left pulmonary artery.
Key takeaways
Persistent left superior vena cava can present with anomalous courses, especially in conjunction with other congenital heart defects like pulmonary agenesis. The aberrant course of the PLSVC in this case was likely influenced by the absence of the left pulmonary artery, highlighting embryological variations.
AI-assisted summary — may contain errors. Verify against the source video. Learn more
More from this webinar
- Acute Pneumocystis jirovecii Pneumonia (PJP)Infection
- Rheumatoid Arthritis with Necrobiotic Nodules complicated by Hydro/Pyopneumothorax and Bronchopleural FistulaAutoimmune
- MALT Lymphoma of the LungNeoplastic
- Hepatopulmonary Syndrome in Dyskeratosis CongenitaMetabolic
- Pulmonary Artery Sarcoma with Pulmonary Vein Involvement and Pulmonary InfarctionNeoplastic
- Post-Operative Unilateral Pulmonary Edema from Left Pulmonary Venous ThrombosisVascular
- Post-Lobectomy Unilateral Pulmonary Edema from Kinked Pulmonary ArteryIatrogenic
- Unilateral Pulmonary Edema in Massive Bilateral Pulmonary Embolism with Lobe SparingVascular
See all cases from October 24, 2014 →
Related Congenital cases
- Lateral Costal Artery Anatomic Variant
- Anomalous Coronary Arteries from the Right Coronary Cusp
- Anomalous Right Coronary Artery from the Left Coronary Cusp with Intramural Course
- Anomalous Left Main Coronary Artery from the Right Coronary Cusp with Retroaortic Course
- Mounier-Kuhn Syndrome
- Williams-Campbell Syndrome