Wells syndrome – an Odyssey

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Abstract

BACKGROUND: Wells syndrome is a rare idiopathic dermatosis of the eosinophilic spectrum. Diagnostic criteria include cutaneous eruptions of variable morphology with eosinophilic infiltrates, peripheral blood eosinophilia, a relapsing, remitting course, and exclusion of systemic disease. Diagnosis is often delayed. CASE PRESENTATION: We present a 28-year older man with recently developed pruritic and sometimes painful erythema. His medical history was positive for coughing in the evening that started in November 2012. Later, a pansinusitis developed. Early diagnosis improves the outcome. CONCLUSION: Standardized treatment has yet to be developed. In our case, systemic corticosteroids were of limited value only.

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Heinig, B., Vojvocic, A., Lotti, T., Tirant, M., & Wollina, U. (2019). Wells syndrome – an Odyssey. Open Access Macedonian Journal of Medical Sciences, 7(18), 3002–3005. https://doi.org/10.3889/oamjms.2019.572

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