Treatment of Eosinophilic Folliculitis
Topical corticosteroids are the first-line treatment for eosinophilic pustular folliculitis, followed by oral indomethacin if topical therapy fails. 1
Types of Eosinophilic Folliculitis
Eosinophilic pustular folliculitis (EPF) has several variants:
- Classic type (Ofuji disease) - most common in Japan
- HIV-associated type
- Infantile type
- Palmoplantar type
- Medication-associated variant
- Neoplasia-associated variant
Diagnostic Approach
A skin biopsy is essential to confirm the diagnosis of EPF, which typically shows:
- Subcorneal eosinophilic and neutrophilic pustules in the follicular infundibulum
- Marked spongiosis of the follicular epithelium
- Perivascular mixed inflammatory cell infiltrate with eosinophils, neutrophils, and lymphocytes 2
Laboratory findings may include:
- Peripheral eosinophilia
- Elevated serum IgE levels
- Negative bacterial and fungal cultures from pustules 2
Treatment Algorithm
First-line Treatment:
- Topical corticosteroids - potent formulations applied twice daily to affected areas 1
Second-line Options (if topical corticosteroids fail):
- Oral indomethacin (50-75 mg/day) - highly effective for classic EPF but can cause peptic ulcers 1, 3
- Topical tacrolimus 0.1% ointment - effective steroid-sparing agent, especially for recurrent cases 4
Additional Treatment Options for Refractory Cases:
HIV-associated EPF specific options:
Other options for resistant cases:
Special Considerations
HIV-associated EPF:
Long-term management:
- EPF is often chronic and recurrent
- Avoid prolonged use of topical steroids due to risk of skin atrophy, hypertrichosis, and dyspigmentation 4
- Consider maintenance therapy with steroid-sparing agents like tacrolimus for recurrent cases
Pathergy phenomenon:
- Some patients develop new lesions at sites of trauma or scratching
- Advise patients to avoid scratching to prevent spread of lesions 2
Monitoring and Follow-up
- Regular follow-up to assess treatment response
- Monitor for side effects of medications (especially gastrointestinal effects with indomethacin)
- Consider alternative therapies if initial treatment fails after 2-4 weeks
- Be prepared for relapses, which are common with this condition
Treatment Pitfalls to Avoid
- Failing to confirm diagnosis with skin biopsy before initiating treatment
- Prolonged use of high-potency topical steroids without considering steroid-sparing alternatives
- Not considering HIV testing in appropriate clinical scenarios
- Overlooking the potential for drug-induced variants of EPF
The diversity of clinical presentations suggests that EPF may be a reaction pattern rather than a single disease entity, so therapy should be tailored to the specific variant and underlying etiology 1.