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Anais Brasileiros de Dermatologia

Print version ISSN 0365-0596On-line version ISSN 1806-4841

Abstract

BRITO, Fernanda Freitas de et al. Ofuji disease: a rare dermatosis and its challenging therapeutic approach. An. Bras. Dermatol. [online]. 2016, vol.91, n.5, pp.646-648. ISSN 1806-4841.  https://doi.org/10.1590/abd1806-4841.20164778.

Eosinophilic pustular folliculitis (EPF) or Ofuji disease is a rare dermatosis, prone to recurrence and chronicity. The peak incidence occurs in the third decade of life and its exact etiology remains unknown. Evidence suggests that the expression of adhesion molecules and the production of cytokines activate the follicular unit, but the stimulus that triggers these changes remains unclear. The three clinical variants reported in the literature include classic EPF, immunosuppression-associated EPF, and infancy-associated EPF. We report a case of eosinophilic pustular folliculitis with peculiar epidemiological characteristics, which represents a challenging therapeutic scenario.

Keywords : Skin Diseases; Pregnancy; HIV; Neutrophil infiltration.

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