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- W2101075411 abstract "Funding sources: none. Conflicts of interest: none declared. Madam, Eosinophilic pustular folliculitis (EPF) was first described in 1970 by Ofuji et al.1 as a condition affecting young Japanese adults, characterized clinically by recurrent crops of sterile, follicular papulopustules affecting the face, trunk and extremities, and histologically by vesiculation of the outer root sheath and eosinophilic infiltration. Three variants of the disorder are now recognized: classic EPF (as originally described by Ofuji et al.), human immunodeficiency virus‐associated EPF, and EPF in infancy, as reported by Lucky et al.2 in 1984. The infantile form has not consistently been proven to demonstrate true follicular involvement, and the term ‘eosinophilic pustulosis’ proposed by Taïeb3 may be preferred. Numerous treatment options for eosinophilic pustulosis of infancy have been documented in case reports, including topical corticosteroids2 and systemic agents such as antihistamines, erythromycin4 and dapsone,5 but the effectiveness of these agents has been variable. We describe two cases in infancy successfully treated with topical tacrolimus." @default.
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- W2101075411 date "2012-10-29" @default.
- W2101075411 modified "2023-09-27" @default.
- W2101075411 title "Treatment of eosinophilic pustulosis of infancy with topical tacrolimus" @default.
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- W2101075411 doi "https://doi.org/10.1111/j.1365-2133.2012.11045.x" @default.
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