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Wells' syndrome: a clinical and histopathologic review of seven cases
Meena Moossavi1, Darius R Mehregan
1Department of Dermatology, Wayne State University, Detroit, Michigan, USA.
Abstract:
Wells' syndrome, or eosinophilic cellulitis, is characterized clinically by an acute dermatitis resembling cellulitis, which evolves into violaceous plaques that resolve spontaneously without scarring. The histopathologic features are dynamic, starting with dermal edema and infiltration of eosinophils, the development of "flame figures," and finishing with the appearance of phagocytic histiocytes. We present the clinical and histopathologic features of seven cases of eosinophilic cellulitis.
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