European Journal of Dermatology
MENUAnnular leukocytoclastic vasculitis in a patient with PR3-antineutrophil cytoplasmic antibody-positive ulcerative colitis Volume 30, issue 4, July-August 2020
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Department of Dermatology, Ruhr-University Bochum, Bochum, Germany
- DOI : 10.1684/ejd.2020.3816
- Page(s) : 420-1
- Published in: 2020
Annular leukocytoclastic vasculitis (ALV), which was firstly described by Degos and Guiliane [1], is a rare clinical variant of leukocytoclastic vasculitis. It can be accompanied by infections, drugs, and several systemic diseases such as ulcerative colitis (UC) [2-4]. Here, we report a patient with proteinase 3 cytoplasmic-anti-neutrophil cytoplasmic antibody (PR3-ANCA)-positive UC who developed ALV accompanied by pauci-immune glomerulonephritis and haemorrhages of the eyes and palate mucosa.A 28-year-old [...]