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Published on: February 9, 2011
[Eosinophilic pustular folliculitis in childhood]
J Luelmo Aguilar1, A Sáez Artacho
1Unidad de Dermatología y Servicio de Anatomía Patológica, Consorcio Sanitario del Parc Taulí, Sabadell, Barcelona, Spain. jluelmo@cspt.es
Insights
Eosinophilic pustular folliculitis (EPF) in infants presents as recurrent scalp pustules. This condition, though rarely reported in children, is likely more common and warrants pediatrician awareness.
Area of Science:
- Pediatric Dermatology
- Inflammatory Skin Disorders
Background:
- Eosinophilic pustular folliculitis (EPF) is an inflammatory skin condition of unknown cause.
- In infants, EPF typically manifests as recurrent sterile pustules on the scalp, sometimes affecting other body areas.
Observation:
- This study details four pediatric cases (7-18 months) with recurrent, itchy papules and pustules on the scalp.
- Lesions were sterile, with negative cultures for bacteria, fungi, and viruses.
- Peripheral eosinophilia was noted in three patients.
Findings:
- Topical steroids provided temporary relief in most cases, with frequent recurrences.
- Antihistamines showed a fair response in steroid-resistant cases.
- No underlying systemic diseases were identified.
Implications:
- Eosinophilic pustular folliculitis (EPF) appears to be a distinct entity in infants.
- The condition may be underdiagnosed in pediatric populations.
- Pediatricians should consider EPF in the differential diagnosis of infantile scalp pustulosis.
Background:
Eosinophilic pustular folliculitis (EPF) is an inflammatory disorder of unknown etiology. In infants this disorder is characterized by recurrent episodes of sterile pustules primarily or exclusively involving the scalp with occasional involvement of the face, trunk and extremities. There are few reports of EPF in children.
Objective:
To describe the clinical features and evolution of four pediatric patients and to discuss the main differential diagnoses.
Methods:
Biopsy specimens were examined, pustules were cultured and laboratory tests were analyzed.
Results:
Four patients (3 males and 1 female) aged 7-18 months presented with self limiting recurrent pruritic papules and pustules on the scalp. In one patient, the lesions were mainly localized on the extremities. Cultures for bacteria, fungi and viruses were negative. No systemic disease was found. Topical steroids were effective in three patients but pustules recurred after treatment was stopped. Cetirizine and Hydroxacen were administered in two corticoid-resistant patients with fair response. No other systemic therapy was administered. Peripheral eosinophilia was detected in three patients.
Conclusions:
EPF in infants seems to be a clearly defined entity. Although few cases have been described in children, this dermatosis is undoubtedly more frequent than suggested by the literature. Consequently, pediatricians should be aware of its existence.
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