Literature DB >> 7732173

Therapy of resistant systemic necrotizing vasculitis. Polyarteritis, Churg-Strauss syndrome, Wegener's granulomatosis, and hypersensitivity vasculitis group disorders.

L H Calabrese1, G S Hoffman, L Guillevin.   

Abstract

The systemic necrotizing vasculitides represent a difficult group of diseases from a therapeutic perspective. Even with successful therapy patients often experience a high degree of disease and treatment morbidity. Refractory disease, or that which fails to respond to standard therapy, is particularly challenging. A clinical approach to several vasculitic syndromes is outlined in this article with emphasis given to therapies supported by controlled investigations and those supported by consensus opinion where available.

Entities:  

Mesh:

Year:  1995        PMID: 7732173

Source DB:  PubMed          Journal:  Rheum Dis Clin North Am        ISSN: 0889-857X            Impact factor:   2.670


  4 in total

Review 1.  Management of virus-induced systemic vasculitides.

Authors:  Loïc Guillevin; Pascal Cohen
Journal:  Curr Rheumatol Rep       Date:  2002-02       Impact factor: 4.592

2.  Churg-Strauss syndrome: the clinical features and long-term follow-up of 17 patients.

Authors:  Mi Jung Oh; Jin Young Lee; Nam Hee Kwon; Dong Chull Choi
Journal:  J Korean Med Sci       Date:  2006-04       Impact factor: 2.153

3.  Eosinophilic granulomatosis with polyangiitis and diffuse gastrointestinal involvement.

Authors:  Diana L Franco; Kevin Ruff; Lester Mertz; Dora M Lam-Himlin; Russell Heigh
Journal:  Case Rep Gastroenterol       Date:  2014-10-28

4.  Not All Gastric Ulcers Are Malignant.

Authors:  Muhammad Sheharyar Warraich; Bashar Attar; Shazaq Khalid
Journal:  Cureus       Date:  2022-07-03
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.