Buch, Englisch, 896 Seiten, Format (B × H): 157 mm x 231 mm, Gewicht: 1361 g
Buch, Englisch, 896 Seiten, Format (B × H): 157 mm x 231 mm, Gewicht: 1361 g
Reihe: Lung Biology in Health and Disease
ISBN: 978-1-4200-5342-5
Verlag: Taylor & Francis Inc
The only text on the market today that deals with the entire spectrum of ILDs, this handy, one-stop reference includes:
- a special focus on treatment and the proper use of treatment options, including in depth coverage of the most common and potentially dangerous means of treatment
- emerging concepts in patient care
- discussion of lung diseases affecting the survivors of 9/11
Zielgruppe
Professional and Professional Reference
Autoren/Hrsg.
Fachgebiete
Weitere Infos & Material
Approach to patient with diffuse interstitial lung disease. Thoracic Imaging for Diffuse ILD and bronchiolar disorders. Bronchoalveolar lavage. (BAL) for Diffuse ILD. Genetics of ILD. Pathology of Diffuse ILD. Immunosuppressive and cytotoxic drug therapy for Diffuse ILD. Sarcoidosis: pathogenesis, epidemiology. Pulmonary Sarcoidosis. Extrapulmonary sarcoidosis. Hypersensitivity pneumonitis. Berylliosis. Hard metal pneumoconiosis. Silicosis and Asbestosis. Idiopathic pulmonary. fibrosis (IPF). Nonspecific Interstitial Pneumonitis. Respiratory bronchiolitis interstitial lung disease (RBILD) and desquamative interstitial pneumonia (DIP). Acute interstitial pneumonia (AIP). Lymphocytic Interstitial Pneumonitis (LIP) and other pulmonary lymphoproliferative disorders. Collagen-vascular disease-associated pulmonary fibrosis. Other pleuropulmonary complications of CVDs. Cryptogenic Organizing Pneumonia (COP) and other causes of organizing pneumonia. Obliterative bronchiolitis: classification, causes, overview. Obliterative bronchiolitis following lung or heart-lung transplantation. Pulmonary complications of bone marrow transplantation. Pulmonary and airway complications related to September 11th. Pathogenesis and Epidemiology of ANCA-associated Vasculitides. Wegener’s Granulomatosis. Churg-Strauss Vasculitis. Microscopic polyangiitis. Pulmonary Capillaritis. Anti-GBM antibody disease (Goodpasture’s Syndrome). Behcet’s Disease. Eosinophilic pneumonias and syndromes. Langerhans cell granulomatosis (LCG). Lymphangioleiomyomatosis. Pulmonary alveolar proteinosis (PAP). Pulmonary and tracheobronchial involvement with amyloidosis. Drug -induced pulmonary disorders.