Wells’ syndrome, also known as eosinophilic cellulitis, consists of nonspecific clinical findings, including cellulitis, urticaria, and inflammatory papules. It has a distinctive histopathologic pattern of eosinophilic infiltration of the dermis and epidermis along with histiocytes and „flame figures“.

        Key words: Wells’ syndrome - eosinophilic cellulitis - recurrent granulomatous dermatitis with eosinophilia