Search

The idiopathic inflammatory myopathies (IIM) are a rare group of autoimmune diseases, negatively affecting the lives of an estimated 250,000 people worldwide. Delays in diagnosis often occur owing to a lack of recognition of disease presentation, or misdiagnosis, both of which can lead to muscle atrophy. This new addition to the Oxford Rheumatology Library series focuses on providing a summary of what is currently understood about the epidemiology of myositis, controversies in diagnosis criteria, clinical features, and the current paradigms for treatment and intervention. Designed to bring together the multi-disciplinary involvement of healthcare professionals for IMM patients, this is the first easy-to-navigate guide for the practical management of myositis. This is an essential guide for both physicians and trainees in Rheumatology, Neurology, and Dermatology specialities.

Representing the most up-to-date knowledge of this family of diseases, this book presents a comprehensive overview of the inflammatory myopathies, including dermatomyositis, polymyositis and inclusion body myositis. The Inflammatory Myopathies covers clinical presentation, diagnosis and classification, ongoing assessment, treatment and pathogenesis. Physical findings, laboratory studies, imaging modalities and biopsy are discussed. The role and mechanism of the inflammatory response is also explored. The Inflammatory Myopathies is the gold-standard in the field, an essential resource for rheumatologists, neurologists and all healthcare professionals who treat afflicted patients.