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ILD Sessions

Bridging Rheumatology and Pulmonology: Advances in the Management of Connective Tissue Diseases (CTD)-Associated ILD
  • Imaging and Biomarkers in CTD-ILD: From Pattern Recognition to Precision Diagnosis
  • Early Detection for Better Outcomes: Who, When, and How to Screen
  • From Inflammation to Fibrosis: Insights into the Immunopathogenesis of CTD-ILD
  • CTD-ILD: What Truly Drives Outcomes – The Underlying Disease, Clinical Presentation, or Imaging Pattern?
  • Therapeutic Evolution in CTD-ILD: Integrating Immunomodulation and Antifibrotic Strategies
  • Systemic sclerosis-associated interstitial lung disease: a conceptual framework for subclinical, clinical and progressive disease
  • The Many Faces of Myositis-Associated Interstitial Lung Disease: From Autoantibodies to Phenotypes
Advances and Challenges in Hypersensitivity Pneumonitis
  • From Immune Response to Recognition: Decoding Diagnostic Clues in HP
  • Integrating Serology and Environmental Assessment in HP Evaluation
  • Current HP Guidelines: Strengths, Shortcomings, and the Path Forward
  • Tailoring Treatment: Determinants of Effective HP Management
  • Fibrotic HP Phenotypes: Implications for Personalized Treatment
Idiopathic Pulmonary Fibrosis (IPF): From Mechanisms to Management
  • Understanding the Roots: Mechanisms Driving Fibrosis in IPF
  • Early and Accurate Diagnosis: Challenges and Opportunities
  • Imaging Insights: HRCT Patterns and the Evolving Role of Quantitative Tools
  • Optimizing Antifibrotic Use and Emerging Therapies in IPF
Controversial entities in Interstitial Lung Diseases
  • Bronchiolocentric Interstitial Pneumonia: A Distinct Entity? – Pro & Con
  • Rare Interstitial Pneumonias (AFOP, ACIF): Do They Deserve Separate Recognition? – Pro & Con
  • Interstitial Pneumonia with Autoimmune Features (IPAF): Still a Useful Concept? – Pro & Con
  • Management of Acute Exacerbations in Non-IPF ILD: Should the Approach Differ? – Pro & Con
  • New ERS/ATS International Multidisciplinary Classification of the Interstitial Pneumonias – Pro & Con
Detecting, Defining, and Managing Progression in Fibrotic Interstitial Lung Disease
  • Are We Getting It Right? The Challenge of Diagnosing Disease Progression in Fibrotic ILDs
  • From Pattern Recognition to Progression Assessment: Imaging Challenges in Fibrosis
  • The Many Faces of Progression: Phenotypic Diversity in Fibrotic ILDs
  • Can Histopathology Predict the Course of Fibrotic Lung Disease?
  • Slowing the Course: Current Approaches to Treating Progressive Fibrosis
Genetic and Familial Interstitial Lung Disorders
  • Familial Pulmonary Fibrosis: Clinical Implications and Therapeutic Options
  • Telomere-Related Genes: Can Pathogenic Variants Guide Prognosis?
  • No Genetic Variants Found — Should Our Approach to Familial Pulmonary Fibrosis Change?
  • Screening Family Members: Who, When, and How?
Rare and Challenging Diffuse Lung Disorders: New Trends and Novel Insights
  • Targeting the mTOR Pathway in Lymphangioleiomyomatosis: From Sirolimus to Next-Generation Therapeutics
  • Redefining Pulmonary Langerhans Cell Histiocytosis: From a Smoking-Related Disorder to a MAPK-Driven Neoplasia
  • Harnessing the GM-CSF Axis in Pulmonary Alveolar Proteinosis: From Whole-Lung Lavage to Targeted Immunotherapy
  • Beyond Corticosteroids: Precision B-Cell-Directed Therapy in IgG4-Related Lung Disease
  • Immune Dysregulation in Focus: Emerging Biomarkers and Biologic Therapies in Granulomatous Lymphocytic Interstitial Lung Disease
  • Olipudase Alfa and Beyond: The New Era of Enzyme Replacement Therapy in Acid Sphingomyelinase-Deficient Niemann-Pick Disease
  • Pleuroparenchymal Fibroelastosis: Unraveling the Enigma of Upper Lobe Fibrosis- Pathogenesis, Diagnosis, and Evolving Therapeutic Insights
Pulmonary Hypertension in Interstitial Lung Disease: Mechanisms, Markers, and Management
  • When Fibrosis Meets Vascular Disease: Pathogenic Pathways of Pulmonary Hypertension in ILD
  • Identifying PH in ILD: From Echocardiography to Right Heart Catheterization
  • Treating the Untreatable? Current and Emerging Therapies for PH-ILD
  • Recognizing and Managing Pulmonary Hypertension in CTD-Associated Interstitial Lung Disease
  • Pulmonary Hypertension in Sarcoidosis: Pathophysiology and Clinical Implications
Comprehensive Non-Pharmacologic Strategies in Fibrotic Interstitial Lung Disease
  • Pulmonary Rehabilitation and Exercise Training: Optimizing Capacity and Quality of Life in Fibrotic ILD
  • Oxygen Therapy and Non-Invasive Ventilatory Support: Bridging Hypoxemia and Comfort
  • Nutritional and Metabolic Support
  • Palliative and Supportive Care: Redefining Goals in Fibrotic Lung Disease
  • Lung Transplantation: The Final Frontier in Fibrotic ILD Management

Keydates

15

MAR

Abstract Submission Deadline

15

APR

Author Notification

11

MAY

Early Bird Registration

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