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Pulmonary fibrosis. --- Alveolitis, Fibrosing --- Diffuse fibrosing alveolitis --- Diffuse interstitial pulmonary fibrosis --- Fibrosing alveolitis --- Hamman-Rich syndrome --- Interstitial fibrosis of the lung --- Interstitial pneumonia --- Interstitial pneumonitis --- Lungs --- Pneumonia, Interstitial --- Pneumonitis, Interstitial --- Fibrosis --- Diseases
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Idiopathic pulmonary fibrosis (IPF) affects 13-20 people per 100,000 population worldwide. In the United States, approximately 100,000 people have IPF with 30,000-40,000 new cases diagnosed annually. Diagnosis remains a challenge with a significant lag between symptoms onset and diagnosis. Delayed diagnosis and treatment can carry high morbidity and mortality. This book provides concise, easy-to-read, and up-to-date information as it relates to clinical presentation, diagnosis, and treatment of IPF. Despite, adequate treatment, the disease progresses, and a lung transplant is necessary in some cases. This book also discusses the role of lung transplants for IPF and its complications. It is a useful resource for primary care physicians, allied health professionals, hospitalists, and pulmonary physicians who take care of patients with IPF.
Pulmonary fibrosis. --- Alveolitis, Fibrosing --- Diffuse fibrosing alveolitis --- Diffuse interstitial pulmonary fibrosis --- Fibrosing alveolitis --- Hamman-Rich syndrome --- Interstitial fibrosis of the lung --- Interstitial pneumonia --- Interstitial pneumonitis --- Lungs --- Pneumonia, Interstitial --- Pneumonitis, Interstitial --- Fibrosis --- Diseases
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This reprint is a compilation of ten publications, including original-research and review articles, and the accompanying editorial within the scope of a Special Issue entitled: "State of the Art in Idiopathic Pulmonary Fibrosis" published in Cells.
Pulmonary fibrosis. --- Alveolitis, Fibrosing --- Diffuse fibrosing alveolitis --- Diffuse interstitial pulmonary fibrosis --- Fibrosing alveolitis --- Hamman-Rich syndrome --- Interstitial fibrosis of the lung --- Interstitial pneumonia --- Interstitial pneumonitis --- Lungs --- Pneumonia, Interstitial --- Pneumonitis, Interstitial --- Fibrosis --- Diseases
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This clinically focused pocket guide offers a concise yet complete overview of idiopathic pulmonary fibrosis, covering the most recent information on aspects such as pathophysiology, management, treatment, and clinical trials. The text is easily accessible and offers pulmonologists and other health care professionals with an excellent quick reference tool. Full color images and figures enhance and summarize key aspects of the text. Idiopathic pulmonary fibrosis is a condition that affects the alveoli and leads to serious lung damage, and the idiopathic nature of this disease means that the origin or cause is unknown. This disease is relatively rare, affecting 3 in 10,000 people, but it is becoming more common. Physicians should be aware of the early stages and symptoms of this disease so management strategies can be implemented quickly, and the best treatment can be administered.
Medicine. --- Respiratory organs --- Medicine & Public Health. --- Pneumology/Respiratory System. --- Diseases. --- Pulmonary fibrosis. --- Alveolitis, Fibrosing --- Diffuse fibrosing alveolitis --- Diffuse interstitial pulmonary fibrosis --- Fibrosing alveolitis --- Hamman-Rich syndrome --- Interstitial fibrosis of the lung --- Interstitial pneumonia --- Interstitial pneumonitis --- Lungs --- Pneumonia, Interstitial --- Pneumonitis, Interstitial --- Fibrosis --- Diseases --- Pneumology. --- Respiratory organs—Diseases.
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"Clinically focused and designed to provide a to-the-point overview, Interstitial Lung Disease, by Drs. Talmadge King, Harold Collard, and Luca Richeldi, bring you up to date with increased understanding, new treatment protocols, and recent advances in the field. Written by contributing specialists who are global experts in their respective areas, this one-stop reference provides pulmonologists, intensivists, internal medicine physicians, and researchers with a dependable source of information on current treatment options and patient care"--Publisher's description.
Interstitial lung diseases. --- Lung Diseases, Interstitial. --- lung Diseases, Interstitial. --- Diffuse Parenchymal Lung Diseases --- Interstitial Lung Diseases --- Pneumonia, Interstitial --- Pneumonitis, Interstitial --- Interstitial Lung Disease --- Interstitial Pneumonia --- Interstitial Pneumonias --- Interstitial Pneumonitides --- Interstitial Pneumonitis --- Lung Disease, Interstitial --- Pneumonias, Interstitial --- Pneumonitides, Interstitial --- Lungs --- Diseases, Interstitial --- Interstitial diseases --- Diseases --- Diffuse Parenchymal Lung Disease
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From epidemiology and pathogenesis to disease management, this book reviews our current understanding of and provides up-to-date information of Idiopathic Pulmonary Fibrosis (IPF). A subtype of Idiopathic Interstitial Pneumonias (IIP), IPF is one of the most elusive and intractable respiratory disease to date and its triggering factors remain unclear. However, new developments such as serum markers that are highly specific to IPF (i.e. KL-6, SP-A, and SP-D), the establishment of systematic diagnostic imaging (HRCT) and accumulated reports of treatment using an antifibrotic agent (pirfenidone) are slowly improving our understanding of the disease. Edited by an established authority in the field and written by experts, this book will be valuable to not only to beginning learners but also to physicians, instructors and researchers whose work involves IIPs. With each chapter exploring critical questions, with unresolved issues and future prospects, the book offers a valuable resource for understanding issues such as the newly proposed entity of interstitial pneumonia with emphysema (combined pulmonary fibrosis and emphysema: CPFE) and the mechanism of how so many IIP sufferers develop lung cancer.
Respiratory System Diseases --- Medicine --- Health & Biological Sciences --- Pulmonary fibrosis. --- Alveolitis, Fibrosing --- Diffuse fibrosing alveolitis --- Diffuse interstitial pulmonary fibrosis --- Fibrosing alveolitis --- Hamman-Rich syndrome --- Interstitial fibrosis of the lung --- Interstitial pneumonia --- Interstitial pneumonitis --- Lungs --- Pneumonia, Interstitial --- Pneumonitis, Interstitial --- Fibrosis --- Diseases --- Pneumology. --- Cytokines. --- Pneumology/Respiratory System. --- Cytokines and Growth Factors. --- Cellular immunity --- Immune response --- Regulation --- Respiratory organs—Diseases. --- Growth factors. --- Cell growth factors --- Cellular growth factors --- Growth peptides --- Growth promoting substances --- Growth substances --- Peptide growth factors --- Peptide regulatory factors --- Polypeptide growth factors --- Cytokines --- Peptides
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Idiopathic Pulmonary Fibrosis: A Comprehensive Clinical Guide delivers a concise review of our current understanding of disease pathogenesis and provides current evidence in the medical literature regarding its diagnosis and management. Each chapter includes key points and a summary aiming to update clinicians about various issues concerning the diagnosis and management of IPF. In addition to outlining the current state of knowledge, each chapter also provides a summary of ongoing research and identifies the needs for future research in the field. Idiopathic Pulmonary Fibrosis: A Comprehensive Clinical Guide is an important new text that provides its readers with a better understanding of the pathobiology and natural history of IPF as it continues to evolve.
Fibrosis. --- Pulmonary fibrosis. --- Alveolitis, Fibrosing --- Diffuse fibrosing alveolitis --- Diffuse interstitial pulmonary fibrosis --- Fibrosing alveolitis --- Hamman-Rich syndrome --- Interstitial fibrosis of the lung --- Interstitial pneumonia --- Interstitial pneumonitis --- Lungs --- Pneumonia, Interstitial --- Pneumonitis, Interstitial --- Fibrosis --- Medicine. --- Internal medicine. --- Respiratory organs --- Primary care (Medicine). --- Medicine & Public Health. --- Pneumology/Respiratory System. --- Internal Medicine. --- Primary Care Medicine. --- Diseases. --- Primary medical care --- Medical care --- Respiratory diseases --- Medicine, Internal --- Medicine --- Clinical sciences --- Medical profession --- Human biology --- Life sciences --- Medical sciences --- Pathology --- Physicians --- Collagen diseases --- Diseases --- Pneumology. --- Emergency medicine. --- Medicine, Emergency --- Critical care medicine --- Disaster medicine --- Medical emergencies --- Respiratory organs—Diseases.
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Granuloma --- Lung Diseases, Interstitial --- Sarcoidosis --- Vasculitis --- Angiitis --- Angiitides --- Vasculitides --- Besnier-Boeck-Schaumann Syndrome --- Boeck Disease --- Boeck's Disease --- Schaumann Disease --- Schaumann Syndrome --- Schaumann's Syndrome --- Besnier-Boeck Disease --- Boeck's Sarcoid --- Besnier Boeck Disease --- Besnier Boeck Schaumann Syndrome --- Boeck Sarcoid --- Boecks Disease --- Boecks Sarcoid --- Disease, Schaumann --- Sarcoid, Boeck's --- Sarcoidoses --- Schaumann's Syndromes --- Syndrome, Besnier-Boeck-Schaumann --- Syndrome, Schaumann --- Syndrome, Schaumann's --- Diffuse Parenchymal Lung Diseases --- Interstitial Lung Diseases --- Pneumonia, Interstitial --- Pneumonitis, Interstitial --- Interstitial Lung Disease --- Interstitial Pneumonia --- Interstitial Pneumonias --- Interstitial Pneumonitides --- Interstitial Pneumonitis --- Lung Disease, Interstitial --- Pneumonias, Interstitial --- Pneumonitides, Interstitial --- Granulomas --- Diffuse Parenchymal Lung Disease
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Sarcoidosis --- Lungs --- Granuloma. --- Lung Diseases, Interstitial. --- Sarcoidosis. --- Vasculitis. --- Ziekte van Besnier-Boeck. --- Diseases --- Diseases. --- Besnier-Boeck disease --- Boeck's sarcoid --- Granuloma benignum --- Lymphogranulomatosis benigna --- Schaumann's disease --- Pulmonary diseases --- Angiitis --- Angiitides --- Vasculitides --- Besnier-Boeck-Schaumann Syndrome --- Boeck Disease --- Boeck's Disease --- Schaumann Disease --- Schaumann Syndrome --- Schaumann's Syndrome --- Besnier-Boeck Disease --- Boeck's Sarcoid --- Besnier Boeck Disease --- Besnier Boeck Schaumann Syndrome --- Boeck Sarcoid --- Boecks Disease --- Boecks Sarcoid --- Disease, Schaumann --- Sarcoid, Boeck's --- Sarcoidoses --- Schaumann's Syndromes --- Syndrome, Besnier-Boeck-Schaumann --- Syndrome, Schaumann --- Syndrome, Schaumann's --- Diffuse Parenchymal Lung Diseases --- Interstitial Lung Diseases --- Pneumonia, Interstitial --- Pneumonitis, Interstitial --- Interstitial Lung Disease --- Interstitial Pneumonia --- Interstitial Pneumonias --- Interstitial Pneumonitides --- Interstitial Pneumonitis --- Lung Disease, Interstitial --- Pneumonias, Interstitial --- Pneumonitides, Interstitial --- Granulomas --- Lung --- Lymphoproliferative disorders --- Pseudotuberculosis --- Tumors --- Cardiopulmonary system --- Chest --- Respiratory organs --- Diffuse Parenchymal Lung Disease
Listing 1 - 9 of 9 |
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