Congenital Cardiothoracic Imaging Cases (continued)
987 cardiothoracic imaging teaching cases categorised as Congenital, each linked to the exact moment in its source webinar video.
- Unicuspid Aortic Valve with Mixed Stenosis and Regurgitation
- Left Pulmonary Agenesis
- Tetralogy of Fallot with Pulmonary Atresia ("Super Tet") and Right Aortic Arch
- High-Flow Mediastinal Vascular Malformation
- Low-Flow (Venous) Mediastinal Vascular Malformation
- Bronchopulmonary Dysplasia with Mosaic Attenuation and Air Trapping
- Congenital Lobar Overinflation (Congenital Lobar Emphysema)
- Retroaortic (Circumaortic) Left Brachiocephalic Vein
- Tracheobronchomegaly (Mounier-Kuhn Syndrome)
- Outflow Tract Ventricular Septal Defect with Anomalous Pulmonary Artery Branch
- Congenital Heart Disease with Hypoplastic Aortic Arch and Diffuse Iliac Artery Hypoplasia
- Patent Ductus Arteriosus Communicating with the False Lumen in a Type B Aortic Dissection
- Recurrent Infected Intralobar Pulmonary Sequestration
- Second Incidentally Discovered Patent Ductus Arteriosus in a Type B Aortic Dissection
- DiGeorge Syndrome with Right Cervical Aortic Arch and Patent Ductus Arteriosus
- Pseudocoarctation of the Aorta with Bicuspid Aortic Valve
- Aortic Coarctation with Disproportionately Dilated Descending Aorta
- Dynamic Free-Breathing CT Airway Evaluation Demonstrating Severe Tracheomalacia
- DiGeorge Syndrome with Absent Thymus and a Cervical Aortic Arch Variant
- Hypoplastic Left Heart Syndrome with a Hypoplastic Ascending Aorta
- Double Aortic Arch with Complete Vascular Ring
- Incidental Pseudocoarctation with a High, Kinked Aortic Arch
- Double Aortic Arch with Atretic Segment Reclassified from Presumed Aberrant Subclavian
- Bronchopulmonary Sequestration with Bronchial Atresia
- Loeys-Dietz Syndrome
- Cervical Aortic Arch with Aberrant Subclavian Artery in DiGeorge Syndrome
- Anomalous Bronchial Artery Origin from the Left Subclavian Artery
- Cervical Aortic Arch with Aberrant Left Subclavian Artery in DiGeorge Syndrome
- Azygos Continuation of the IVC with Bilateral Hyparterial Bronchi and Polysplenia-like Anatomy
- Proximal Interruption of the Right Pulmonary Artery with Severe Pulmonary Hypertension
- Primary Ciliary Dyskinesia (Kartagener Syndrome) with Situs Inversus and Bronchiectasis
- Tuberous Sclerosis with Cardiac Lipomas, Renal/Hepatic Angiomyolipomas, and Pulmonary LAM
- Isolated Main Pulmonary Artery Aneurysm from a Quadricuspid Pulmonic Valve
- Left Pre-hyparterial Accessory Bronchus
- Anomalous Systemic Arterial Supply to the Right Lower Lobe
- Cor Triatriatum Sinister with Levoatrial Cardinal Vein
- Non-Obstructive Cor Triatriatum Sinister
- Left Upper Lobe Partial Anomalous Pulmonary Venous Return
- Mixed Total Anomalous Pulmonary Venous Return
- Mounier-Kuhn Syndrome
- Pulmonary Arteriovenous Malformation with Brain Abscess
- Congenital Absence of the Left Pericardium
- Congenitally Corrected Transposition of the Great Arteries
- Lymphangioleiomyomatosis in Tuberous Sclerosis
- Birt-Hogg-Dube Syndrome
- Diaphragmatic Eventration
- Double Aortic Arch
- Hereditary Hemorrhagic Telangiectasia-Associated Pulmonary Hypertension
- Congenital Pulmonary Airway Malformation
- Total Anomalous Pulmonary Venous Return