https://doi.org/10.4081/reumatismo.2019.1252
Erysipelas-like presentation of Wells’ syndrome (eosinophilic cellulitis)
Submitted: 30 August 2019
Accepted: 19 October 2019
Published: 28 January 2020
Accepted: 19 October 2019
Abstract Views: 1315
PDF: 718
Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
Authors
Wells’ syndrome, also called eosinophilic cellulitis, is a rare eosinophilic dermatosis characterized by an unspecific inflammatory erythematous eruption often associated with systemic symptoms. Here we report the case of a 57-year-old female with bilateral painful pitting and pruritic feet progressive for two weeks despite one week of oral antibiotics. Skin biopsy was performed showing dermal eosinophilic infiltration. The patient showed a spontaneous progressive improvement of the condition. The presented case demonstrates both clinical and histologic presence of lesions of Wells’ syndrome in the course of the disease. A careful diagnostic approach is needed because of the lack of specific signs. The global outcome is favorable and spontaneous resolution is possible.
How to Cite
Belfeki, N., Gharbi, E., Flateau, C., & Diamantis, S. (2020). Erysipelas-like presentation of Wells’ syndrome (eosinophilic cellulitis). Reumatismo, 71(4), 226–229. https://doi.org/10.4081/reumatismo.2019.1252
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