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- W2035473228 endingPage "516" @default.
- W2035473228 startingPage "507" @default.
- W2035473228 abstract "Wegener's granulomatosis (WG) is an idiopathic, systemic inflammatory disease characterized by necrotizing granulomatous inflammation and pauci-immune small-vessel vasculitis of upper and lower respiratory tract and kidneys. The condition affects both genders equally, although some inconsistent gender differences have been observed. The aetiology of WG remains unknown although a number of exogenous factors have been suggested to be of aetiological relevance. Most clinical characteristics of this disease are non-specific, making clinical diagnosis challenging. Histopathological examination of lesional and peritoneal tissue is not pathognomonic, but is an essential investigation to confirm the presence of disease and exclude other disorders. At present, despite the increasingly wide range of potential therapies, cyclophosphamide plus corticosteroids remain the most recognized and effective means of inducing and sustaining remission of WG." @default.
- W2035473228 created "2016-06-24" @default.
- W2035473228 creator A5001255902 @default.
- W2035473228 creator A5015883457 @default.
- W2035473228 creator A5057610879 @default.
- W2035473228 creator A5088010459 @default.
- W2035473228 date "2013-01-10" @default.
- W2035473228 modified "2023-10-16" @default.
- W2035473228 title "Wegener's granulomatosis: a review of clinical features and an update in diagnosis and treatment" @default.
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