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Written and edited by global leaders in this challenging field, Rare and Interstitial Lung Diseases: Clinical Cases and Real-World Discussions brings you up to date with the latest advances in complex or rare lung diseases managed on outpatient or inpatient respiratory or critical care units. Using a unique, case-based approach, a wide variety of cases are presented along with perspectives from a multidisciplinary team of experts who discuss therapeutic choices and rationales. This real-world approach allows the reader to become a virtual attending physician, simulating a realistic clinical reasoning process on the diagnosis, treatment, and follow-up of patients with rare and complex lung diseases.

  • Reflects a nuanced, multidisciplinary, evidence-based approach to diagnoses, treatment options, and follow-up criteria for complex and rare pulmonary disorders such as idiopathic pulmonary fibrosis, interstitial lung disease related to connective tissue diseases, hypersensitivity pneumonitis, sarcoidosis, and pulmonary vascular disease.
  • Each case includes onset of symptoms, diagnostic/therapeutic path, and discussions on the clinical choices made in accordance with evidence-based medical procedures.
  • Describes each clinical and laboratory finding and features 150 images, including plain film, procedural photos, ultrasound images, CT scans, and histopathology specimens.
  • Includes the most recent updates to international guidelines (ATS/ERS/JRS/ALAT) on idiopathic pulmonary fibrosis (IPF).
  • Covers the progression of pulmonary fibrosis in patients with ILD other than IPF; the role of transbronchial lung cryobiopsy (TBLC) in obtaining a tissue diagnosis in patients with undiagnosed ILD; and the indications of antifibrosant drugs.
  • A practical and interactive resource for pulmonologists, as well as critical care and internal medicine practitioners and fellows, thoracic surgeons, and thoracic radiologists.
  • Any additional digital ancillary content may publish up to 6 weeks following the publication date.

1. Cover image - p. Cover 2. Title page - p. ii 3. Table of Contents - p. iii 4. Inside front cover - p. iii 5. Copyright - p. iii 6. Contributors - p. iii 7. Foreword - p. iii 8. Preface - p. iii 9. How to use - p. iii 10. Contents - p. iii 11. Video contents - p. iii 12. List of Illustrations - p. iii 13. List of Tables - p. iii 14. PART I: Fibrosing Interstitial Lung Diseases - p. iii 15. Chapter 1: Fibrotic hypersensitivity pneumonitis after long-term exposure to household mold - p. iii 16. Chapter 2: Idiopathic pulmonary fibrosis with a typical usual interstitial pneumonia pattern on chest high-resolution computed tomography - p. 12 17. Chapter 3: Idiopathic pulmonary fibrosis in a smoker with indeterminate usual interstitial pneumonia pattern on high-resolution computed tomography - p. 21 18. Chapter 4: Interstitial lung abnormalities evolving to histologically proven nonspecific interstitial pneumonia - p. 31 19. PART II: Smoking-Associated Interstitial Lung Diseases - p. 44 20. Chapter 5: Respiratory bronchiolitis-interstitial lung disease - p. 44 21. Chapter 6: Desquamative interstitial pneumonia complicated by glucocorticoid-induced osteonecrosis of the femoral head in a former smoker - p. 56 22. Chapter 7: Pulmonary langerhans cell histiocytosis in a young man complaining of a dry cough and exertional dyspnea - p. 66 23. Chapter 8: Combined pulmonary fibrosis and emphysema in a smoker with apparently normal lung volumes - p. 79 24. PART III: Granulomatous Lung Diseases - p. 92 25. Chapter 9: Swollen cervical lymph nodes and centrilobular pulmonary nodules due to sarcoidosis - p. 92 26. Chapter 10: Relapsing pulmonary infiltrates, severe asthma, and eosinophilia with systemic manifestations - p. 108 27. Chapter 11: Diffuse parenchymal lung disease with granulomas in the colon and cervical lymph nodes due to tuberculosis - p. 121 28. PART IV: Connective Tissue Disease–Associated Lung Diseases - p. 133 29. Chapter 12: Pulmonary fibrosis and solitary pulmonary nodule in hidden rheumatoid arthritis - p. 133 30. Chapter 13: Interstitial lung disease with high-resolution computed tomography pattern of usual interstitial pneumonia in a patient with unknown systemic sclerosis - p. 145 31. Chapter 14: Interstitial lung disease associated with the antisynthetase syndrome - p. 157 32. PART V: Rare and Ultra-Rare Interstitial Lung Diseases - p. 169 33. Chapter 15: Pulmonary alveolar microlithiasis: An ultra-rare disease - p. 169 34. Chapter 16: Pulmonary alveolar proteinosis in a woman with respiratory failure and crazy-paving pattern on chest computed tomography - p. 180 35. Chapter 17: Idiopathic pleuroparenchymal fibroelastosis in a never-smoker woman with a history of hypersensitivity pneumonitis - p. 192 36. Chapter 18: IgG4-related disease as an unexpected cause of hemoptysis - p. 205 37. PART VI: Miscellanea - p. 217 38. Chapter 19: Amyloid-associated cystic lung disease in a woman with Sjögren syndrome - p. 217 39. Chapter 20: Sporadic lymphangioleiomyomatosis in a woman previously diagnosed with asthma - p. 228 40. Chapter 21: Acute respiratory failure in a patient with diffuse ground-glass opacities during the COVID-19 pandemic - p. 242 41. Index - p. 256 42. Inside back cover - p. 256

Descripcion
Descripción

Written and edited by global leaders in this challenging field, Rare and Interstitial Lung Diseases: Clinical Cases and Real-World Discussions brings you up to date with the latest advances in complex or rare lung diseases managed on outpatient or inpatient respiratory or critical care units. Using a unique, case-based approach, a wide variety of cases are presented along with perspectives from a multidisciplinary team of experts who discuss therapeutic choices and rationales. This real-world approach allows the reader to become a virtual attending physician, simulating a realistic clinical reasoning process on the diagnosis, treatment, and follow-up of patients with rare and complex lung diseases.

  • Reflects a nuanced, multidisciplinary, evidence-based approach to diagnoses, treatment options, and follow-up criteria for complex and rare pulmonary disorders such as idiopathic pulmonary fibrosis, interstitial lung disease related to connective tissue diseases, hypersensitivity pneumonitis, sarcoidosis, and pulmonary vascular disease.
  • Each case includes onset of symptoms, diagnostic/therapeutic path, and discussions on the clinical choices made in accordance with evidence-based medical procedures.
  • Describes each clinical and laboratory finding and features 150 images, including plain film, procedural photos, ultrasound images, CT scans, and histopathology specimens.
  • Includes the most recent updates to international guidelines (ATS/ERS/JRS/ALAT) on idiopathic pulmonary fibrosis (IPF).
  • Covers the progression of pulmonary fibrosis in patients with ILD other than IPF; the role of transbronchial lung cryobiopsy (TBLC) in obtaining a tissue diagnosis in patients with undiagnosed ILD; and the indications of antifibrosant drugs.
  • A practical and interactive resource for pulmonologists, as well as critical care and internal medicine practitioners and fellows, thoracic surgeons, and thoracic radiologists.
  • Any additional digital ancillary content may publish up to 6 weeks following the publication date.

1. Cover image - p. Cover 2. Title page - p. ii 3. Table of Contents - p. iii 4. Inside front cover - p. iii 5. Copyright - p. iii 6. Contributors - p. iii 7. Foreword - p. iii 8. Preface - p. iii 9. How to use - p. iii 10. Contents - p. iii 11. Video contents - p. iii 12. List of Illustrations - p. iii 13. List of Tables - p. iii 14. PART I: Fibrosing Interstitial Lung Diseases - p. iii 15. Chapter 1: Fibrotic hypersensitivity pneumonitis after long-term exposure to household mold - p. iii 16. Chapter 2: Idiopathic pulmonary fibrosis with a typical usual interstitial pneumonia pattern on chest high-resolution computed tomography - p. 12 17. Chapter 3: Idiopathic pulmonary fibrosis in a smoker with indeterminate usual interstitial pneumonia pattern on high-resolution computed tomography - p. 21 18. Chapter 4: Interstitial lung abnormalities evolving to histologically proven nonspecific interstitial pneumonia - p. 31 19. PART II: Smoking-Associated Interstitial Lung Diseases - p. 44 20. Chapter 5: Respiratory bronchiolitis-interstitial lung disease - p. 44 21. Chapter 6: Desquamative interstitial pneumonia complicated by glucocorticoid-induced osteonecrosis of the femoral head in a former smoker - p. 56 22. Chapter 7: Pulmonary langerhans cell histiocytosis in a young man complaining of a dry cough and exertional dyspnea - p. 66 23. Chapter 8: Combined pulmonary fibrosis and emphysema in a smoker with apparently normal lung volumes - p. 79 24. PART III: Granulomatous Lung Diseases - p. 92 25. Chapter 9: Swollen cervical lymph nodes and centrilobular pulmonary nodules due to sarcoidosis - p. 92 26. Chapter 10: Relapsing pulmonary infiltrates, severe asthma, and eosinophilia with systemic manifestations - p. 108 27. Chapter 11: Diffuse parenchymal lung disease with granulomas in the colon and cervical lymph nodes due to tuberculosis - p. 121 28. PART IV: Connective Tissue Disease–Associated Lung Diseases - p. 133 29. Chapter 12: Pulmonary fibrosis and solitary pulmonary nodule in hidden rheumatoid arthritis - p. 133 30. Chapter 13: Interstitial lung disease with high-resolution computed tomography pattern of usual interstitial pneumonia in a patient with unknown systemic sclerosis - p. 145 31. Chapter 14: Interstitial lung disease associated with the antisynthetase syndrome - p. 157 32. PART V: Rare and Ultra-Rare Interstitial Lung Diseases - p. 169 33. Chapter 15: Pulmonary alveolar microlithiasis: An ultra-rare disease - p. 169 34. Chapter 16: Pulmonary alveolar proteinosis in a woman with respiratory failure and crazy-paving pattern on chest computed tomography - p. 180 35. Chapter 17: Idiopathic pleuroparenchymal fibroelastosis in a never-smoker woman with a history of hypersensitivity pneumonitis - p. 192 36. Chapter 18: IgG4-related disease as an unexpected cause of hemoptysis - p. 205 37. PART VI: Miscellanea - p. 217 38. Chapter 19: Amyloid-associated cystic lung disease in a woman with Sjögren syndrome - p. 217 39. Chapter 20: Sporadic lymphangioleiomyomatosis in a woman previously diagnosed with asthma - p. 228 40. Chapter 21: Acute respiratory failure in a patient with diffuse ground-glass opacities during the COVID-19 pandemic - p. 242 41. Index - p. 256 42. Inside back cover - p. 256

Indice
Autores
Muestra
Ficha Técnica