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Eosinophilic cellulitis (Wells' syndrome) is an uncommon inflammatory disease with clinical polymorphism. It is often associated with infectious, allergic or myeloproliferative diseases; however, the exact aetiology is unknown. This report describes a rare case of eosinophilic cellulitis in association with angioimmunoblastic lymphadenopathy. The typical skin findings of Wells' syndrome disappeared completely following chemotherapy and autologous stem cell transplantation. [ABSTRACT FROM AUTHOR]

The article presents a case study of a 45-year-old man with a history of fever and erythema of the extremities, the presence of lymphocytes and eosinophils were detected. It notes the demonstration of blood neutrophilia and the increased C-reactive protein, the impact of coxsackievirus A6 infection, and diagnosis of the patient for Wells' syndrome.

The article describes the case of eosinophilic cellulitis (EC) in a 68-year-old man induced by administration of interferon (IFN)-Β. Immunohistochemical staining for p signal transducers and activator of transcription (pSTAT) and pSTAT6 for 3 cases of ordinary, idiopathic EC. It found that repeated local injection of IFN-Β may have generated matured dendritic cell (DC) at the injection site.