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Anti-Neutrophil Cytoplasmic Antibody (Anca) Associated Vasculitis 2020 Edition
Contributor(s): Sinico, Renato Alberto (Editor), Guillevin, Loic (Editor)
ISBN: 3030022382     ISBN-13: 9783030022389
Publisher: Springer
OUR PRICE:   $123.49  
Product Type: Hardcover
Published: October 2019
Qty:
Temporarily out of stock - Will ship within 2 to 5 weeks
Additional Information
BISAC Categories:
- Medical | Rheumatology
- Medical | Nephrology
- Medical | Immunology
Dewey: 616.079
Series: Rare Diseases of the Immune System
Physical Information: 0.74" H x 7.16" W x 9.49" (1.40 lbs) 336 pages
 
Descriptions, Reviews, Etc.
Publisher Description:

This volume, written by well-known experts in the field, covers all aspects of Anti-Neutrophil Cytoplasmic Antibody (ANCA) Associated Vasculitis (AAV). The expression refers to a group of diseases, characterized by destruction and inflammation of small vessels. The clinical signs vary and affect several organs, such as the kidney, lung, skin, nervous system and others.

The opening chapters give some historical hints, explain the genetic basis of the disease and provide insights into the pathogenesis derived from recent experimental studies and guides the reader through classification and nomenclature. A large part of the book is then devoted to a detailed description of the specific related diseases and their clinical presentations, the disease course, and potential complications. The advice regarding treatment is based on the best currently available evidence in this constantly evolving area.

The book is part of Springer's series Rare Diseases of the Immune System, which presents recently acquired knowledge on pathogenesis, diagnosis, and therapy with the aim of promoting a more holistic approach to these conditions. AAVs are systemic autoimmune diseases of unknown cause that affect small (to medium) sized blood vessels. They include granulomatosis with polyangiitis (formerly Wegener's granulomatosis), microscopic polyangiitis, and eosinophilic granulomatosis with polyangiitis (formerly Churg-Strauss syndrome).

This volume will be an invaluable source of up-to-date information for all practitioners involved in the care of patients with these diseases.