Literature DB >> 3066099

[Wegener's granulomatosis: classification and therapy].

R A De Remee1.   

Abstract

Wegener's granulomatosis in its classic form is manifested by necrotizing granulomas of the upper and lower respiratory tract, focal necrotizing vasculitis involving both arteries and veins which may be widely disseminated, and focal necrotizing glomerulitis. The disease may present with incomplete expression involving any combination of the major sites, including the upper respiratory tract (E), the lung (L), or the kidney (K). A newly emerging test for the disease called antineutrophil cytoplasmic antibody (ANCA) shows promise in studying the disease in its various expressions. Standard current treatment includes glucocorticoids and cyclophosphamide. Recently, favorable reports of improvement on trimethoprim/sulfamethoxazole combination have appeared, suggesting the possibility that the disease may be incited by a microbial infection.

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Year:  1988        PMID: 3066099

Source DB:  PubMed          Journal:  Acta Med Austriaca        ISSN: 0303-8173


  2 in total

Review 1.  Wegener's granulomatosis. Thoughts and observations of a pathologist.

Authors:  F Wegener
Journal:  Eur Arch Otorhinolaryngol       Date:  1990       Impact factor: 2.503

2.  Polyangiitis overlap syndrome with features of Wegener's granulomatosis and panarteriitis nodosa.

Authors:  C Brunner; R Kain; W Köhler; M Weissel
Journal:  Klin Wochenschr       Date:  1991-05-24
  2 in total

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