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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.
  • Enhanced eBook version included with purchase. Your enhanced eBook allows you to access all of the text, figures, and references from the book on a variety of devices. Additional digital ancillary content may publish up to 6 weeks following the publication date.

1. Cover image - p. i 2. Title page - p. ii 3. Table of Contents - p. iii 4. Copyright - p. iv 5. Contributors - p. v 6. Foreword - p. ix 7. Preface - p. xi 8. List of Illustrations - p. xvii 9. List of Tables - p. xviii 10. Videos - p. xviii 11. PART I. Fibrosing Interstitial Lung Diseases - p. 1 12. 1.  Fibrotic hypersensitivity pneumonitis after long-term exposure to household mold - p. 3 13. 2.  Idiopathic pulmonary fibrosis with a typical usual interstitial pneumonia pattern on chest high-resolution computed tomography - p. 13 14. 3.  Idiopathic pulmonary fibrosis in a smoker with indeterminate usual interstitial pneumonia pattern on high-resolution computed tomography - p. 23 15. 4.  Interstitial lung abnormalities evolving to histologically proven nonspecific interstitial pneumonia - p. 33 16. PART II. Smoking-Associated Interstitial Lung Diseases - p. 45 17. 5.  Respiratory bronchiolitis-interstitial lung disease - p. 47 18. 6.  Desquamative interstitial pneumonia complicated by glucocorticoid-induced osteonecrosis of the femoral head in a former smoker - p. 57 19. 7.  Pulmonary langerhans cell histiocytosis in a young man complaining of a dry cough and exertional dyspnea - p. 69 20. 8.  Combined pulmonary fibrosis and emphysema in a smoker with apparently normal lung volumes - p. 81 21. PART III. Granulomatous Lung Diseases - p. 95 22. 9.  Swollen cervical lymph nodes and centrilobular pulmonary nodules due to sarcoidosis - p. 97 23. 10.  Relapsing pulmonary infiltrates, severe asthma, and eosinophilia with systemic manifestations - p. 111 24. 11.  Diffuse parenchymal lung disease with granulomas in the colon and cervical lymph nodes due to tuberculosis - p. 123 25. PART IV. Connective Tissue Disease–Associated Lung Diseases - p. 135 26. 12.  Pulmonary fibrosis and solitary pulmonary nodule in hidden rheumatoid arthritis - p. 137 27. 13.  Interstitial lung disease with high-resolution computed tomography pattern of usual interstitial pneumonia in a patient with unknown systemic sclerosis - p. 147 28. 14.  Interstitial lung disease associated with the antisynthetase syndrome - p. 159 29. PART V. Rare and Ultra-Rare Interstitial Lung Diseases - p. 171 30. 15.  Pulmonary alveolar microlithiasis: An ultra-rare disease - p. 173 31. 16.  Pulmonary alveolar proteinosis in a woman with respiratory failure and crazy-paving pattern on chest computed tomography - p. 183 32. 17.  Idiopathic pleuroparenchymal fibroelastosis in a never-smoker woman with a history of hypersensitivity pneumonitis - p. 193 33. 18.  IgG4-related disease as an unexpected cause of hemoptysis - p. 207 34. PART VI. Miscellanea - p. 219 35. 19.  Amyloid-associated cystic lung disease in a woman with Sjögren syndrome - p. 221 36. 20.  Sporadic lymphangioleiomyomatosis in a woman previously diagnosed with asthma - p. 231 37. 21.  Acute respiratory failure in a patient with diffuse ground-glass opacities during the COVID-19 pandemic - p. 245 38. Index - p. 257

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.
  • Enhanced eBook version included with purchase. Your enhanced eBook allows you to access all of the text, figures, and references from the book on a variety of devices. Additional digital ancillary content may publish up to 6 weeks following the publication date.

1. Cover image - p. i 2. Title page - p. ii 3. Table of Contents - p. iii 4. Copyright - p. iv 5. Contributors - p. v 6. Foreword - p. ix 7. Preface - p. xi 8. List of Illustrations - p. xvii 9. List of Tables - p. xviii 10. Videos - p. xviii 11. PART I. Fibrosing Interstitial Lung Diseases - p. 1 12. 1.  Fibrotic hypersensitivity pneumonitis after long-term exposure to household mold - p. 3 13. 2.  Idiopathic pulmonary fibrosis with a typical usual interstitial pneumonia pattern on chest high-resolution computed tomography - p. 13 14. 3.  Idiopathic pulmonary fibrosis in a smoker with indeterminate usual interstitial pneumonia pattern on high-resolution computed tomography - p. 23 15. 4.  Interstitial lung abnormalities evolving to histologically proven nonspecific interstitial pneumonia - p. 33 16. PART II. Smoking-Associated Interstitial Lung Diseases - p. 45 17. 5.  Respiratory bronchiolitis-interstitial lung disease - p. 47 18. 6.  Desquamative interstitial pneumonia complicated by glucocorticoid-induced osteonecrosis of the femoral head in a former smoker - p. 57 19. 7.  Pulmonary langerhans cell histiocytosis in a young man complaining of a dry cough and exertional dyspnea - p. 69 20. 8.  Combined pulmonary fibrosis and emphysema in a smoker with apparently normal lung volumes - p. 81 21. PART III. Granulomatous Lung Diseases - p. 95 22. 9.  Swollen cervical lymph nodes and centrilobular pulmonary nodules due to sarcoidosis - p. 97 23. 10.  Relapsing pulmonary infiltrates, severe asthma, and eosinophilia with systemic manifestations - p. 111 24. 11.  Diffuse parenchymal lung disease with granulomas in the colon and cervical lymph nodes due to tuberculosis - p. 123 25. PART IV. Connective Tissue Disease–Associated Lung Diseases - p. 135 26. 12.  Pulmonary fibrosis and solitary pulmonary nodule in hidden rheumatoid arthritis - p. 137 27. 13.  Interstitial lung disease with high-resolution computed tomography pattern of usual interstitial pneumonia in a patient with unknown systemic sclerosis - p. 147 28. 14.  Interstitial lung disease associated with the antisynthetase syndrome - p. 159 29. PART V. Rare and Ultra-Rare Interstitial Lung Diseases - p. 171 30. 15.  Pulmonary alveolar microlithiasis: An ultra-rare disease - p. 173 31. 16.  Pulmonary alveolar proteinosis in a woman with respiratory failure and crazy-paving pattern on chest computed tomography - p. 183 32. 17.  Idiopathic pleuroparenchymal fibroelastosis in a never-smoker woman with a history of hypersensitivity pneumonitis - p. 193 33. 18.  IgG4-related disease as an unexpected cause of hemoptysis - p. 207 34. PART VI. Miscellanea - p. 219 35. 19.  Amyloid-associated cystic lung disease in a woman with Sjögren syndrome - p. 221 36. 20.  Sporadic lymphangioleiomyomatosis in a woman previously diagnosed with asthma - p. 231 37. 21.  Acute respiratory failure in a patient with diffuse ground-glass opacities during the COVID-19 pandemic - p. 245 38. Index - p. 257

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Ficha Técnica