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[Eruptive pseudoangiomatosis in infant and newborns]
B Guillot1, H Chraibi, C Girard
1Service de Dermatologie, Hôpital Saint-Eloi, CHU de Montpellier. b.guillot@chu-montpellier.fr
Insights
Eruptive pseudoangiomatosis presents as a rash in infants, often following infections. This study highlights varied presentations and disease courses, suggesting a non-specific viral cause.
Area of Science:
- Pediatric Dermatology
- Infectious Diseases
Background:
- Eruptive pseudoangiomatosis (EPA) is an acute, non-pruritic rash in children, typically resolving within days.
- A viral etiology is suspected but remains unproven for EPA.
Observation:
- Seven infants (5 male, 2 female, aged 8 days to 16 months) presented with EPA.
- Typical rash distribution involved face and limbs in 6/7 infants; one had facial and back involvement.
- Rash onset followed infections in 4 cases; one case appeared post-nephroma surgery, and another had familial occurrence.
Findings:
- Six patients experienced spontaneous resolution within 3-10 days; one had a prolonged course (>9 months).
- Infectious agent screening was negative in the two tested children.
- Unique cases included a neonate, a child with renal tumor, and familial rash.
Implications:
- EPA presents diverse clinical scenarios, including very young infants, co-occurrence with tumors, and familial cases.
- This series reinforces EPA as a clinical presentation of non-specific viral infections, similar to Giannotti-Crosti syndrome.
- Further research is needed to identify specific causative agents for eruptive pseudoangiomatosis.
Introduction:
Eruptive pseudoangiomatosis was first described in children in the form of an acute non-pruritic macular or papular rash that fades on application of a glass test and resolves within several days. Viral aetiology is suspected but has never been demonstrated to date.
Observations:
We discuss seven cases of infants presenting this disease: 5 boys and 2 girls aged 8 days to 16 months. The rash presented typical clinical features in all cases and affected the face and limbs in 6 of the 7 subjects. In one child, involvement of the face and back was observed with sparing of the limbs. The rash occurred after an episode of rhinolaryngeal infection in 3 cases and after gastrointestinal infection in 1 case. Spontaneous resolution was seen within 3 to 10 days in 6 patients although a longer course lasting over 9 months was observed in one infant. In another patient, the rash appeared after surgery for mesoblastic nephroma. In one child, a similar rash was seen in both parents. Screening for infectious agents was negative for the two children from whom samples were obtained.
Discussion:
This series of paediatric cases of eruptive pseudoangiomatosis is characterised by the very young age of one of the children, coexistence of the condition with a renal tumour in another child, the familial nature of the rash in a third child and unusually long disease duration in the final child. However, this series did not allow identification of the causative infectious agent or agents. Probably, as with other syndromes such as Giannotti-Crosti syndrome or "gloves and socks" syndrome, eruptive pseudoangiomatosis forms a clinical picture common to a non-specific viral infection.
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