Diffuse Parenchymal Lung Disease
(Sprache: Englisch)
Diffuse parenchymal lung disease (DPLD) represents a large and heterogeneous group of disorders. Although new insights into the pathogenesis and new techniques such as high-resolution-CT have led to a better understanding of DPLD, clinical management...
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Diffuse parenchymal lung disease (DPLD) represents a large and heterogeneous group of disorders. Although new insights into the pathogenesis and new techniques such as high-resolution-CT have led to a better understanding of DPLD, clinical management remains a challenge.
This volume is designed to become a valuable aid in the diagnosis and management of DPLD. It starts with general topics such as a new classification system for DPLD, the general diagnostic approach, and clinical evaluation of the patient by radiology, histological patterns and bronchoalveolar lavage. This is followed by consideration of some basic aspects such as the genetics of DPLD, the principles of granuloma formation, pulmonary fibrogenesis and vasculitis, as well as novel treatment approaches. A large part of the book consists of disease-specific chapters, which discuss granulomatous disorders, idiopathic pulmonary fibrosis and other entities of idiopathic interstitial pneumonia, the collagen vascular diseases, drug-induced infiltrative lung disease as well as orphan diffuse lung diseases including Langerhans' cell histiocytosis, lymphangioleiomyomatosis and pulmonary alveolar proteinosis. Special chapters on DPLD in children and lung transplantation for end-stage fibrosis complete this comprehensive publication.
Written by internationally known experts, this well-organized volume is recommended to a wide audience including respiratory physicians in training, practice and research as well as radiologists and pulmonary pathologists.
Klappentext zu „Diffuse Parenchymal Lung Disease “
Diffuse parenchymal lung disease (DPLD) represents a large and heterogeneous group of disorders. Although new insights into the pathogenesis and new techniques such as high-resolution-CT have led to a better understanding of DPLD, clinical management remains a challenge. This volume is designed to become a valuable aid in the diagnosis and management of DPLD. It starts with general topics such as a new classification system for DPLD, the general diagnostic approach, and clinical evaluation of the patient by radiology, histological patterns and bronchoalveolar lavage. This is followed by consideration of some basic aspects such as the genetics of DPLD, the principles of granuloma formation, pulmonary fibrogenesis and vasculitis, as well as novel treatment approaches. A large part of the book consists of disease-specific chapters, which discuss granulomatous disorders, idiopathic pulmonary fibrosis and other entities of idiopathic interstitial pneumonia, the collagen vascular diseases, drug-induced infiltrative lung disease as well as orphan diffuse lung diseases including Langerhans' cell histiocytosis, lymphangioleiomyomatosis and pulmonary alveolar proteinosis. Special chapters on DPLD in children and lung transplantation for end-stage fibrosis complete this comprehensive publication. Written by internationally known experts, this well-organized volume is recommended to a wide audience including respiratory physicians in training, practice and research as well as radiologists and pulmonary pathologists.
Inhaltsverzeichnis zu „Diffuse Parenchymal Lung Disease “
Foreword; Preface; General Aspects; Classification of Diffuse Parenchymal Lung Disease: Gomez, A.D.; King, T.E., Jr.; Diagnostic Approach to Diffuse Parenchymal Lung Disease: Lynch, J.P., III; Weight, S.S.; Fishbein, M.C.; Clinical Evaluation: Yang, S.; Raghu, G.; Imaging: Desai, S.R.; Wells, A.U.; Diffuse Parenchymal Lung Diseases - Histopathologic Patterns: Chilosi, M.; Murer, B.; Poletti, V.; Bronchoalveolar Lavage: Drent, M.; Baughman, R.P.; Meyer, K.C.; Basic Aspects; Genetics of Interstitial Lung Disease: du Bois, R.M.; Granuloma Formation: Facco, M.; Miorin, M.; Agostini, C.; Semenzato, G.; Pathogenesis of Idiopathic Pulmonary Fibrosis: Noble, P.W.; Basics of Pulmonary Vasculitis: Cohen Tervaert, J.W.; Damoiseaux, J.G.M.C..; Novel Aspects of Treatment for Interstitial Lung Diseases: Behr, J.; Diseases; Sarcoidosis: Newman, L.S.; Wasfi, Y.S.; Hypersensitivity Pneumonitis: Vogelmeier, C.; Idiopathic Pulmonary Fibrosis: Keating, D.T.K.; McCullagh, B.; Egan, J.J.; Nonspecific Interstitial Pneumonia: Flaherty, K.R.; Martinez, F.J.; Diseases: Other Entities of the Idiopathic Interstitial Pneumonias: Collard, H.R.; Pulmonary Fibrosis in Collagen Vascular Disease: Hoyles, R.K.; Wells, A.U.; Pulmonary Vasculitis: Lynch, J.P., III; Fishbein, M.C.; White, E.S.; Drug-Induced and Iatrogenic Infiltrative Lung Disease: Camus, P.; Idiopathic Eosinophilic Pneumonias: Lazor, R.; Cordier, J.-F.; Diffuse Alveolar Hemorrhage: Olson, A.L.; Schwarz, M.I.; Pulmonary Langerhans' Cell Histiocytosis: Harari, S.; Caminati, A.; Lymphangioleiomyomatosis: Johnson, S.R.; Acquired Idiopathic Pulmonary Alveolar Proteinosis: Costabel, U.; Bauer, P.C.; Guzman, J.; Bronchiolitis: Poletti, V.; Casoni, G.; Zompatori, M.; Chilosi, M.; Lymphoproliferative Lung Disorders: Poletti, V.; Zinzani, P.L.; Tomassetti, S.; Chilosi, M.; Special Considerations; Interstitial Lung Diseases in Children: Clement, A.; Fauroux, B.; Lung Transplantation for Diffuse Parenchymal Lung Disease: Irani, S.; Boehler, A.;
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Bibliographische Angaben
- 2007, 348 Seiten, mit farbigen Abbildungen, Maße: 21,5 x 28,7 cm, Gebunden, Englisch
- Herausgegeben von Costabel, U.; du Bois, R. M.; Egan, J. J.; Herth, F. J. F.
- Herausgegeben: U. Costabel, R. M. du Bois, J. J. Egan
- Verlag: Karger
- ISBN-10: 380558153X
- ISBN-13: 9783805581530
Sprache:
Englisch
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