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Recurrent cutaneous eosinophilic vasculitis characterized by annular purpuric lesions: A case report
Paolo Gisondi1, Davide Geat1,2, Chiara Colato3
1Section of Dermatology, Department of Medicine, University of Verona, Verona, Italy.
Abstract:
A 71-year-old woman presented with a persistent, intensely pruritic cutaneous eruption localized on the palmoplantar regions, lips and palate. The histological findings allowed to make the diagnosis of recurrent cutaneous eosinophilic vasculitis, a very rare cutaneous vasculitis characterized clinically by multiple erythematous or purpuric erythematous papules or plaques or angioedema with a relapsing course in the absence of systemic involvement and histologically by a necrotizing vasculitis of the dermal small vessels with a dominant eosinophilic infiltration. The patient was treated with oral methylprednisolone and pentoxifylline which led to a rapid resolution of the cutaneous lesions.
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