@article{Belfeki_Gharbi_Flateau_Diamantis_2020, title={Erysipelas-like presentation of Wells’ syndrome (eosinophilic cellulitis)}, volume={71}, url={https://www.reumatismo.org/reuma/article/view/1252}, DOI={10.4081/reumatismo.2019.1252}, abstractNote={<p>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.</p>}, number={4}, journal={Reumatismo}, author={Belfeki, N. and Gharbi, E. and Flateau, C. and Diamantis, S.}, year={2020}, month={Jan.}, pages={226–229} }