Granulomatosis with polyangiitis classification: Difference between revisions
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!style="background:#4479BA; color: #FFFFFF;" align="center" |American College of Rheumatology (ACR) Classification of Granulomatosis with polyangiitis | !style="background:#4479BA; color: #FFFFFF;" align="center" |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) | | style="background:#F5F5F5;"|Abnormal urinary sediment ( red cell casts or > 5 red blood cells per hpf) | ||
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|Abnormal Chest radiography findings (nodules, cavities, or fixed infiltrates) | | style="background:#F5F5F5;"|Abnormal Chest radiography findings (nodules, cavities, or fixed infiltrates) | ||
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|Nasal discharge or oral ulcers | | style="background:#F5F5F5;"|Nasal discharge or oral ulcers | ||
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|Biopsy that presents with granulomatous inflammation | | style="background:#F5F5F5;"|Biopsy that presents with granulomatous inflammation | ||
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2 out of 4 criteria are needed to distinguish Granulomatosis with polyangiitis | 2 out of 4 criteria are needed to distinguish Granulomatosis with polyangiitis from other vasculitides, with a senstivity of 88% and senstivity of 92%. | ||
==References== | ==References== | ||
Revision as of 14:44, 27 March 2018
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Granulomatosis with polyangiitis Microchapters |
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Differentiating Granulomatosis with polyangiitis from other Diseases |
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Diagnosis |
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Treatment |
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Case Studies |
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Granulomatosis with polyangiitis classification On the Web |
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American Roentgen Ray Society Images of Granulomatosis with polyangiitis classification |
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Directions to Hospitals Treating Granulomatosis with polyangiitis |
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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 from other vasculitides, with a senstivity of 88% and senstivity of 92%.
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.