CTICases679 Congenital Cardiothoracic Imaging Cases
679 cardiothoracic imaging teaching cases categorised as Congenital, each linked to the exact moment in its source webinar video.
- Infundibular Pulmonary Stenosis with Selective Left Pulmonary Artery Enlargement
- Morgagni Hernia Containing Omental Fat
- Poland Syndrome
- Infected Congenital Pulmonary Airway Malformation
- Hybrid CPAM with Bronchial Atresia
- Patent Ductus Arteriosus with Severe Pulmonary Hypertension
- Patent ductus arteriosus (PDA) with massive pulmonary artery aneurysm
- Right Hemi-diaphragm Eventration and Phrenic Nerve Dysfunction
- Persistent Patent Ductus Arteriosus (PDA)
- Persistent Levoatrial Cardinal Vein
- Mixed Type Total Anomalous Pulmonary Venous Return (TAPVR)
- Large Morgagni Hernia
- Esophageal Duplication Cyst
- Total Anomalous Pulmonary Venous Return (TAPVR)
- Double Outlet Right Ventricle (DORV)
- Failed Scimitar Syndrome Repair
- Esophageal Lung
- Warden Procedure for PAPVR
- Tetralogy of Fallot with Systemic Arterial Supply
- Congenital Bronchial Atresia
- Hybrid CPAM/Bronchial Atresia
- Thoracic Duct Lymphatic Malformation/Cyst
- Anatomical Variation: Medial Basal Segment Origin
- Bronchopulmonary Dysplasia
- Total Anomalous Pulmonary Venous Return (TAPVR) - Mixed Type
- Partial Partial Anomalous Pulmonary Venous Return
- Repaired Scimitar Syndrome with Horseshoe Lung
- Scimitar Syndrome
- Hemitruncus Arteriosus
- Accessory Hemidiaphragm
- Williams-Campbell Syndrome
- Anomalous Pulmonary Venous Drainage
- Complicated Scimitar Syndrome Repair
- Cystic Hygroma (Lymphatic Malformation)
- Spontaneous Pneumothorax in Marfan Syndrome
- SMAD4-Associated HHT
- Slow-Flow Vascular Malformation
- Left SVC Draining to Left Atrium
- Venous Malformation of the Chest Wall
- Complex Congenital Heart Disease - Norwood Procedure
- Infracardiac TAPVR
- Eisenmenger Syndrome
- Cystic Fibrosis (Post-Trikafta Therapy)
- Lymphangiectasia vs. Lymphangiomatosis
- Birt-Hogg-Dubé Syndrome
- Alpha-1 Antitrypsin Deficiency
- Aborted Tracheal Bronchus
- Hereditary Parsonage-Turner Syndrome
- Hepatic/Renal Polycystic Disease and Eventration
- Systemic Arterialization to the Left Lower Lobe