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Sarcoidosis
Highly Commended, BMA Medical Book Awards 2013Sarcoidosis represents a major challenge for physicians-not just in respiratory medicine, but across a range of specialties. This book, with a multidisciplinary authorship of the highest standard, presents the most up-to-date thinking on all aspects of the condition, from epidemiology to clinical manife
Pulmonary Sarcoidosis
Pulmonary Sarcoidosis: A Guide for the Practicing Clinician is a valuable resource for clinicians of varied disciplines concerning the care of the sarcoidosis patient. Sarcoidosis is a multi-system disorder and represents a major challenge to physicians. Although any organ may be involved with sarcoidosis, the lung is the most common organ affected. Chapters are written by distinguished authors who have extensive experience in caring for these patients. Detailed figures and tables are provided to guide the practicing clinician through all aspects of the condition, from clinical manifestations to treatment options. Pulmonary Sarcoidosis: A Guide for the Practicing Clinician is fully comprehensive and evidence-based and will be an essential addition to the bookshelves of all whose practice involves the care and treatment of patients with sarcoidosis.
Sarcoidosis
Get a quick, expert overview of the etiology, diagnosis, and management of pulmonary and extra pulmonary sarcoidosis with this concise, practical resource. Drs. Robert B. Baughman and Dominique Valeyre fully cover the recent advances in various aspects of this disease, including new genetic studies and new diagnostic techniques. It's an ideal resource for pulmonologists and respiratory medicine specialists, as well as primary care physicians and pulmonary/respiratory care nurses. - Provides a comprehensive discussion of the various facets of sarcoidosis, including common manifestations of the lung, skin, and eyes, as well as other important aspects such as cardiac and neurologic disease. - Covers newer diagnostic techniques for the lungs and elsewhere in the body, each discussed in detail and compared to older diagnostic techniques. - Discusses treatment options including anti-inflammatory drugs, and management of other aspects of the disease, such as pulmonary hypertension, fatigue, and small fiber neuropathy. - Consolidates today's available information and experience in this important area into one convenient resource.
Sarcoidosis
Since the first edition of this book in 1967, interest in sarcoidosis has increased world-wide, leading to increasing numbers of published clinical, epidemiological and laboratory studies, notably in immunology and in the pathogenesis of granulomatous inflammation. Aseries of international con ferences which started as an informal gathering in London in. 1958 has continued at approximately three-yearly intervals with increasing numbers of participants and more formal organisation, and the proceedings of all but the first have been published. When the preparation of a second edition was suggested to me, I consi dered several questions. ls there still a piace for a comprehensive, clinically or...
Sarcoidosis and Granulomatosis
Sarcoidosis is a multi-organ, granulomatous disease the etiology of which remains unknown. It is characterized by T-cell dysfunction and B-cell hyperactivity with increased local immune activity and inflammation that leads to the formation of noncaseating granulomas in the organs involved. The lung and lymphatic system are the most commonly affected organs, however virtually any organ may be affected. Other common sites of involvement include the skin, eye, central nervous system, and the heart. Patients may present different symptoms related to the disease stage and the specific organ involved. Sarcoidosis is a global disease, and its prevalence has increased twofold over the past years. Due to the clinical heterogeneity and variable diagnostic criteria in different countries, it is difficult to calculate the exact prevalence and incidence of sarcoidosis. Age, sex, race, and geographic origin significantly influence the incidence of sarcoidosis. The book at hand seeks to assess the current diagnostic techniques, imaging techniques, differential diagnosis of this disease, as well as other granulomatous diseases mimicking sarcoidosis.
Atlas of Sarcoidosis
- Comprehensive illustrative encyclopedia containg many rare images - Includes clinical analysis for the physician - Designed to complement and provide a visual supplement to already existing texts on sarcoidosis - Only atlas of sarcoidosis which reviews the multisystmeic nature of sarcoidosis on the context of clinical medicine - Written by world reknown experts in sarcoidosis
Clinical Focus Series: Lesions of Sarcoidosis
Sarcoidosis is a rare condition that causes small patches of red and swollen tissue, called granulomas, to develop in the organs of the body. It most often affects the lungs and skin. Typical symptoms include tender, red bumps on the skin, shortness of breath and a persistent cough. There is no cure for sarcoidosis, but the condition often improves without treatment within a few months or years. Sarcoidosis is estimated to affect about 1 in every 10,000 people in the UK (NHS Choices). Part of the Clinical Focus Series, this book provides trainees with an overview of this complex condition. Beginning with an introduction and guidance on recognising pulmonary granulomas, the following chapters...
Idiopathic Pulmonary Fibrosis
Idiopathic pulmonary fibrosis (IPF) is a steadily progressive and ultimately fatal disease of unknown origin. Recent years have seen advances in our understanding of IPF and a number of guidelines have been published. But many questions remain unanswered, particularly surrounding probable versus definite IPF. This Monograph aims to discuss the latest achievements in IPF, and covers key diagnostic issues, staging of the disease, complications and comorbidities, treatment, unmet patient needs and perspectives for the future. This book will be of interest to all clinicians and researchers in this area.
Controversies in COPD
COPD is one of the most common diseases worldwide and is projected to be the third leading cause of death by 2020. But that does not mean it is easy to understand or manage. In everyday practice, pulmonologists face areas of controversy in COPD, for which evidence-based medicine is often unavailable. This ERS Monograph considers where the current controversies in COPD lie, discussing areas such as screening, premature birth, asthma–COPD overlap syndrome, treatment, rehabilitation and palliative care. This book will be of great interest to both clinicians and scientists, and aims to stimulate further discussion about this diverse and fascinating disease. "...contains a vast amount of information on the disease, its prevalence, signs and symptoms, diagnositc tests and treatment options. The book's format makes it quick and simple to find out what you need to know, and its size would make it easy to take to work for use in practice [...] invaluable for anyone working with patients with the disease." Emma Vincent, Nursing Standard
Clinical Manifestations, Pathophysiology, Diagnostic Methods, Imaging and Intervention in Sarcoidosis
Sarcoidosis is a multisystem granulomatous disease of unknown etiology that is characterised by noncaseous epithelioid cell granulomas, which may affect almost any organ in the body. Intrathoracic involvement is common and accounts for most of the morbidity and mortality associated with this disease. The diagnosis is based on the total exclusion of other granulomatous disorders. The organs that are commonly involved are the lymph nodes, lungs, liver, spleen, skin, and eyes; these organs can be involved individually or in combination. The correlation of the clinical, radiological features along with the pathologic finding of non-caseating epithelioid cell granulomas is vital to establish the ...
