CTICases304 ILD Cardiothoracic Imaging Cases
304 cardiothoracic imaging teaching cases categorised as ILD, each linked to the exact moment in its source webinar video.
- Trimethoprim-Sulfamethoxazole (Bactrim)-Induced Acute Eosinophilic Pneumonia Progressing to ARDS and Fibrosis
- Recurrent Interstitial Lung Disease Post-Transplant
- Radiation-Induced Organizing Pneumonia
- Respiratory Bronchiolitis
- Radiation-Induced Organizing Pneumonia
- Rheumatoid Lung Disease
- Bronchiolocentric Interstitial Pneumonia (BIP) in CVID
- Anti-Synthetase Syndrome (PL-12 Antibody)
- Smoking-Related Interstitial Lung Disease
- Mixed ILD/Silicosis
- Anti-MDA5 Positive Interstitial Lung Disease
- Pleuroparenchymal Fibroelastosis (PPFE)
- Recurrent Fibrotic NSIP in Scleroderma
- Possible Chronic Eosinophilic Pneumonia with Fibrosis
- Radiation-Induced Lung Injury
- Hot Tub Lung (MAC infection)
- Connective Tissue Disease (Limited Scleroderma) Presenting as Fibrotic DIP
- Organizing Pneumonia
- Lupus-Associated Lung Disease
- Pulmonary Langerhans Cell Histiocytosis (PLCH)
- Nitrofurantoin Toxicity
- Sjögren's Syndrome with Hypersensitivity Pneumonitis Features
- Cystic Lung Disease in Connective Tissue Disease
- Mixed Connective Tissue Disease with NSIP and Follicular Bronchiolitis
- Cystic Lung Disease (Differential)
- Airway-Centered Fibrosis
- Exuberant Honeycombing / Airspace Expansion
- Anti-Synthetase Syndrome
- Hypersensitivity Pneumonitis (HP) presenting with emphysema
- Fibrotic Lung Disease
- Mixed Sarcoidosis and UIP
- Anti-Synthetase Syndrome
- Interstitial Lung Abnormalities (ILA)
- Pulmonary Interstitial Emphysema / Cystic Lung Disease
- Acute Exacerbation of Fibrotic ILD
- Chronic Hypersensitivity Pneumonitis (Byssinosis)
- Fibrotic Hypersensitivity Pneumonitis
- Pulmonary Langerhans Cell Histiocytosis (PLCH)
- Expiratory Collapse of Lower Lobe Cystic Airspaces
- Idiopathic Airway-Centered Fibrosis
- Diffuse Panbronchiolitis
- Straight Edge Sign in CTD-ILD
- Antisynthetase Syndrome (Anti-EJ/glycyl-tRNA synthetase)
- Antisynthetase Syndrome (Anti-Jo-1)
- Familial Pulmonary Fibrosis (Genetic Anticipation)
- Lupus-Associated Interstitial Lung Disease (Fibrotic NSIP with Cystic Changes)
- Recurrent Lymphangioleiomyomatosis (LAM) Post-Lung Transplant
- Resolving Post-COVID Diffuse Alveolar Damage
- Non-Specific Interstitial Pneumonia (NSIP)
- Surfactant Protein C Mutation-Associated Pulmonary Fibrosis