Erythema dyschromicum perstans in prepubertal children
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Updated: Aug 10, 2026

Minimal Erythema Dose (MED) Testing
Published on: May 28, 2013
Nanette B Silverberg1, Joshua Herz, Annette Wagner
1St. Luke's-Roosevelt Hospital Center, New York, New York 10025, USA. nsilverberg@slrhc.org
Insights
Erythema dyschromicum perstans (EDP) in children often resolves spontaneously within 2-3 years, unlike the adult form. This study found complete clearance in most pediatric patients, suggesting a different clinical course for childhood EDP.
Area of Science:
- Dermatology
- Pediatrics
- Pigmentation Disorders
Background:
- Erythema dyschromicum perstans (EDP) is a rare pigmentary disorder with an unclear etiology and clinical course in children.
- Adult EDP typically has a slow onset and rarely resolves spontaneously.
Purpose of the Study:
- To define the etiology and clinical course of childhood (prepubertal) Erythema dyschromicum perstans.
- To compare the presentation and resolution of pediatric EDP with the adult form.
Main Methods:
- Retrospective chart review and telephone interviews of eight pediatric patients diagnosed with EDP.
- Analysis of clinical data including onset, duration, and treatment, with a focus on long-term follow-up.
Main Results:
- Five of eight pediatric patients achieved complete resolution of EDP within an average of 2.5 years.
- EDP onset in pediatric patients was noted between July and December.
- Aminopenicillin administration was coincident with EDP development in two cases.
Conclusions:
- Childhood (prepubertal) EDP demonstrates a distinct clinical course compared to adult EDP, with a high likelihood of spontaneous resolution within 2-3 years.
- The findings suggest that pediatric EDP is a self-limiting condition, contrasting with the chronic nature often seen in adults.
Abstract:
Erythema dyschromicum perstans (EDP) is a rare disorder of pigmentation that is most common in Hispanic patients. In adults, EDP has a slow onset and is unlikely to resolve spontaneously. The etiology and clinical course in children is poorly defined. Physical examinations, chart reviews, and telephone interviews were performed for eight pediatric patients with EDP who were followed at Children's Memorial Hospital in Chicago between 1990 and 1998. All the patients available for long-term follow-up (five of the eight) experienced complete clearance without recurrence in an average of 2.5 years. In all of our patients, the onset was noted from July to December. The administration of aminopenicillins was coincident with the development of EDP in two of the patients. Review of the English-language literature reveals that 25 prepubertal children have previously been reported. Including our patients, 69% of prepubertal children with EDP experienced resolution. We concluded that the clinical course of childhood (prepubertal) EDP differs from that of adult EDP, and it is more likely to resolve within 2-3 years.
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