CTICasesILD Cardiothoracic Imaging Cases (continued)
303 cardiothoracic imaging teaching cases categorised as ILD, each linked to the exact moment in its source webinar video.
- Langerhans Cell Histiocytosis and Desquamative Interstitial Pneumonia
- Fibrotic Hypersensitivity Pneumonitis
- Granulomatous-Lymphocytic Interstitial Lung Disease (GLILD) in CVID
- Non-Fibrotic Hypersensitivity Pneumonitis
- Pulmonary Interstitial Emphysema in Dermatomyositis-Associated Interstitial Lung Disease and Diffuse Alveolar Damage
- E-cigarette or Vaping Product Use-Associated Lung Injury presenting as Acute Eosinophilic Pneumonia
- Fish Antigen Hypersensitivity Pneumonitis
- Chronic Eosinophilic Pneumonia with Residual Fibrosis
- Combined Pulmonary Fibrosis and Emphysema (CPFE) in a Never-Smoker
- Rheumatoid Arthritis-Associated Interstitial Lung Disease (UIP with Exuberant Honeycombing)
- Progressive Systemic Sclerosis with Pulmonary Ossification
- Anti-MDA5 and PL-7 Positive Amyopathic Dermatomyositis Presenting as Acute Lung Injury
- Atezolizumab-Induced Organizing Pneumonia
- Durvalumab-Induced Pneumonitis
- Reversible Smoking-Related Respiratory Bronchiolitis
- Pulmonary Langerhans Cell Histiocytosis
- Desquamative Interstitial Pneumonia in Scleroderma
- Nitrofurantoin-Induced Organizing Pneumonia
- Chronic Hypersensitivity Pneumonitis
- Autoimmune Interstitial Lung Disease (IPAF / UIP Pattern)
- GATA2 Deficiency with Follicular Bronchiolitis and Cystic Lung Destruction
- Anti-MDA5 ILD (Rapidly Progressive Interstitial Lung Disease)
- Radiation Pneumonitis post-SABR
- Fibrotic Hypersensitivity Pneumonitis
- Fibrotic Hypersensitivity Pneumonitis with Granulomas
- Immunotherapy-Induced Organizing Pneumonia Evolving to NSIP
- Pleuroparenchymal Fibroelastosis
- Anti-MDA5 Antibody-Associated Interstitial Lung Disease
- Pulmonary Alveolar Proteinosis Progressing to Fibrosis
- Rapidly Progressive Hypersensitivity Pneumonitis
- Pulmonary Alveolar Proteinosis Progressing to Fibrosis
- Chronic Pulmonary Alveolar Proteinosis with Atypical and Fibrotic Patterns
- Progressive NSIP-Pattern Fibrosis Suspecting Connective Tissue Disease
- Granulomatous-Lymphocytic Interstitial Lung Disease in CVID
- Cellular NSIP in IPAF
- Rheumatoid Arthritis Associated UIP with NSIP-like CT Pattern
- Rheumatoid Arthritis Associated Advanced Cystic Fibrotic Lung Disease
- Bronchiolocentric Fibrosis in Connective Tissue Disease
- Antisynthetase Syndrome mimicking COVID-19
- Scleroderma-Associated UIP with Exuberant Honeycombing
- Young-Onset Pleuroparenchymal Fibroelastosis
- Dynamic Expiratory Air Trapping post-Lung Transplant
- Pleuroparenchymal Fibroelastosis
- Unclassifiable Interstitial Lung Disease
- Acute Exacerbation of Idiopathic Pulmonary Fibrosis
- Airway-Centric Hypersensitivity Pneumonitis
- Desquamative Interstitial Pneumonia
- Combined Pulmonary Fibrosis and Emphysema with Spontaneous Pneumothorax
- Stage-Stage NSIP with Transient PA filling defects
- Dendriform Pulmonary Ossification in UIP