Les manifestations cutanées du syndrome hyperéosinophilique sont polymorphes et difficiles à traiter : étude de cohorte rétrospective

Idiopathic hypereosinophilic syndrome with eosinophilic cellulitis-like cutaneous involvement treated with mepolizumab and dapsone

“…3 Cutaneous manifestations are nonspecific, including angioedema, urticaria, eczematous and lichenoid eruptions, prurigo-like lesions, as well as bullous lesions. 3 Eosinophilic cellulitis (Wells syndrome) is a distinct eosinophilic dermatosis typically presenting with cellulitis-like plaques that can last for weeks or years and heal without scarring. 4 Hypereosinophilia may be present, but no other organ is involved beside the skin as opposed to HES.…”