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Hypereosinophilic syndrome (HES) is defined by presence of persistent blood eosinophilia (hypereosinophilia [HE] count >1.5 g/L) or tissue eosinophilia; organ damage or dysfunction attributable to tissue HE; and exclusion of other explanations for organ dysfunction. In primary (neoplastic or lymphoid) HES, eosinophils are clonal (chronic eosinophilic leukemia, a myeloid disorder, or both). In secondary (reactive) HES, eosinophilic expansion has been induced by eosinophilopoietic cytokines. Usually a Th2 T-cell subset of lymphocytes overproduces interleukin-5. A few patients with secondary HES evolve to develop T-cell lymphomas.
A retrospective study of 21 patients found 48% had an atopic history (eczema, asthma, or rhinosinusitis). Skin find…