A case report reveals isolated facial ulceration in granulomatosis with polyangiitis, highlighting diagnostic challenges.
Granulomatosis with polyangiitis (GPA) is a multiorgan system disease process in which cutaneous involvement is not uncommon. However, this article reports a case of GPA that presented with an unusually destructive chronic cutaneous facial lesion without other characteristic organ changes to suggest GPA, which represented a unique diagnostic challenge. It highlights the importance of maintaining high suspicion for vasculitic disease processes and prompt diagnosis to reduce disease burden.
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Smith et al. (2026) studied this question.
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