Granulomatosis with polyangiitis classification: Difference between revisions
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==Overview== | ==Overview== | ||
According to the American College of Rheumatology (ACR) Granulomatosis with polyangiitis is classified using 4 criteria. | According to the American College of Rheumatology (ACR) Granulomatosis with polyangiitis is classified using 4 criteria. |
Revision as of 15:07, 25 November 2016
Granulomatosis with polyangiitis Microchapters |
Differentiating Granulomatosis with polyangiitis from other Diseases |
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Diagnosis |
Treatment |
Case Studies |
Granulomatosis with polyangiitis classification On the Web |
American Roentgen Ray Society Images of Granulomatosis with polyangiitis classification |
Directions to Hospitals Treating Granulomatosis with polyangiitis |
Risk calculators and risk factors for Granulomatosis with polyangiitis classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Ali Poyan Mehr, M.D. [2];Associate Editor(s)-in-Chief: Krzysztof Wierzbicki M.D. [3]
Overview
According to the American College of Rheumatology (ACR) Granulomatosis with polyangiitis is classified using 4 criteria.
Classification
According to the American College of Rheumatology (ACR) Granulomatosis with polyangiitis is classified by 4 criteria. They are:[1]
American College of Rheumatology (ACR) Classification of Granulomatosis with polyangiitis |
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Abnormal urinary sediment ( red cell casts or > 5 red blood cells per hpf) |
Abnormal Chest radiography findings (nodules, cavities, or fixed infiltrates) |
Nasal discharge or oral ulcers |
Biopsy that presents with granulomatous inflammation |
2 out of 4 criteria are needed to distinguish Granulomatosis with polyangiitis form other vasculitides.
References
- ↑ Leavitt RY, Fauci AS, Bloch DA, Michel BA, Hunder GG, Arend WP; et al. (1990). "The American College of Rheumatology 1990 criteria for the classification of Wegener's granulomatosis". Arthritis Rheum. 33 (8): 1101–7. PMID 2202308.