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Anca-Associated Vasculitides: Immunological and Clinical Aspects 1993 Edition
Contributor(s): Gross, Wolfgang L. (Editor)
ISBN: 0306445735     ISBN-13: 9780306445736
Publisher: Springer
OUR PRICE:   $313.49  
Product Type: Hardcover - Other Formats
Published: November 1993
Qty:
Additional Information
BISAC Categories:
- Medical | Cardiology
- Medical | Hematology
- Medical | Immunology
Dewey: 616.13
LCCN: 93005858
Series: Advances in Experimental Medicine and Biology
Physical Information: 1.25" H x 6.14" W x 9.21" (2.15 lbs) 552 pages
 
Descriptions, Reviews, Etc.
Publisher Description:
WEGENER'S GRANULOMATOSIS & ANCA-ASSOCIATED DISEASES: THE STORY CONTINUES The disease now designated as Wegener's granulomatosis (WG) was first described in 1931 by Heinz Klinger, who considered it to be a special form of polyarteritis nodosa. Klinger's friend, Friedrich Wegener, expanded on the first observations and interpreted the pathological and clinical fmdings to represent a distinct disease entity (Wegener, 1939). He described this entity as a "peculiar rhinogenous granulomatosis with a unique participation of the arterial system and the kidneys". Later, Godman and Churg (1954) established the classical diagnostic criteria (the "WG triad"): granuloma, vasculitis, and glomerulonephritis. In 1958 Walton pointed out the poor prognosis of WG based on a small number of published cases (mean survival time: 5 months). In 1966 Carrington and Liebow reported "limited forms" of WG with a defmitely more favorable prognosis. Since then positive results have been reported with cyclophosphamide therapy. In addition, a retrospective study of combined low-dose cyclophosphamide and prednisolone in 85 WG patients over a period of 21 years found a similarly encouraging outcome. The-latter experience led to the current "standard" treatment protocol (FAUCI et al., 1973 and 1983). More recently, strong evidence has emerged that some of the morbidity and mortality ofWG - and other types of systemic vasculitis - may be a consequence of this treatment (Hoffman et al., 1992).