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Relapsing granulomatosis with polyangiitis with severe lung and upper respiratory tract involvement successfully treated with rituximab
Granulomatosis with polyangiitis (GPA) is a chronic, relapsing, primary systemic small vessel vasculitis associated with anti-neutrophil cytoplasmic antibodies. The disease is characterised by the involvement of various organs. The relapse rate rises from about 20% at 12 months to about 60% at 5 yea...
保存先:
| 出版年: | Reumatologia |
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| 主要な著者: | , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Narodowy Instytut Geriatrii, Reumatologii i Rehabilitacji w Warszawie
2017
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5647538/ https://ncbi.nlm.nih.gov/pubmed/29056777 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5114/reum.2017.69783 |
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