Granulomatosis with polyangiitis: A case report and brief review of literature
- PMID: 34527120
- PMCID: PMC8429614
- DOI: 10.1016/j.radcr.2021.08.028
Granulomatosis with polyangiitis: A case report and brief review of literature
Erratum in
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Erratum regarding missing declaration of competing interest and patient consent statements in previously published articles.Radiol Case Rep. 2023 Jan 24;18(3):1394-1395. doi: 10.1016/j.radcr.2023.01.018. eCollection 2023 Mar. Radiol Case Rep. 2023. PMID: 36819000 Free PMC article.
Abstract
Granulomatosis with polyangiitis formerly known as Wegener's granulomatosis was first described by German pathologist Friedrich Wegener in 1936. It is a multi-system necrotizing noncaseating granulomatous vasculitis which affects small to medium-sized vessels. It can involve any organ system, most commonly the lungs and kidneys. American College of Rheumatology requires 2 of 4 criteria for diagnosis: Positive biopsy for granulomatous vasculitis, urinary sediment with red blood cells, abnormal chest radiograph and oral/nasal inflammation. Here we present a case of Granulomatosis with polyangiitis with brief review of literature.
Keywords: Granulomatosis with polyangiitis; Vasculitis; Wegener's granulomatosis.
© 2021 The Authors. Published by Elsevier Inc. on behalf of University of Washington.
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