Abstract
Eosinophilic pustular folliculitis (EPF) is a rare cutaneous disorder that typically occurs in three clinical contexts: men, individuals who are immunosuppressed or have human immunodeficiency virus, and infants. A fourth subtype occurring 2 to 3 months after hematopoietic stem cell transplantation (HSCT) has recently been described in several adults. We report two cases of EPF arising in children after HSCT. It is important to recognize this form of EPF after HSCT and differentiate it from graft-versus-host disease since it responds readily to topical steroids and appears to have an excellent prognosis.
© 2017 Wiley Periodicals, Inc.
MeSH terms
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Child
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Diagnosis, Differential
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Eosinophilia / diagnosis*
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Eosinophilia / drug therapy
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Eosinophilia / etiology
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Folliculitis / diagnosis*
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Folliculitis / drug therapy
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Folliculitis / etiology
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Glucocorticoids / therapeutic use*
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Graft vs Host Disease / diagnosis*
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Humans
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Immunosuppressive Agents / adverse effects*
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Infant
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Infant, Newborn
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Male
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Skin / pathology
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Skin Diseases, Vesiculobullous / diagnosis*
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Skin Diseases, Vesiculobullous / drug therapy
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Skin Diseases, Vesiculobullous / etiology
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Stem Cell Transplantation / adverse effects*
Substances
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Glucocorticoids
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Immunosuppressive Agents
Supplementary concepts
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Eosinophilic pustular folliculitis