# Hydroa Vacciniforme: A Rare Pediatric Photodermatosis

**Authors:** Mouna Guechchati, Hanane Baybay, Meryem Zeryouhi, Layla Tahiri Elousrouti, FatimaZahra Mernissi

PMC · DOI: 10.7759/cureus.82079 · Cureus · 2025-04-11

## TL;DR

This paper describes a rare skin condition in a child caused by a virus and managed with sun protection.

## Contribution

The study presents a new clinical case of hydroa vacciniforme with detailed diagnostic and management insights.

## Key findings

- The patient showed chronic photodermatosis linked to Epstein-Barr virus infection.
- Strict photoprotection led to sustained remission over two years.
- Histopathology and immunohistochemistry confirmed characteristic lymphoid infiltrates and EBV involvement.

## Abstract

Hydroa vacciniforme (HV) is a rare, chronic photodermatosis linked to Epstein-Barr virus (EBV) infection. We report a 12-year-old child with recurrent vesiculobullous facial lesions and photosensitivity for six years. Clinical examination revealed hemorrhagic crusts with atrophic scars. Dermoscopy showed whitish streaks and rosettes. Histopathology demonstrated epidermal spongiosis and a dense dermal lymphoid infiltrate. Immunohistochemistry confirmed CD3+, CD5+, CD7+, and CD8+ lymphocytes, with granzyme B and perforin expression, but no CD56. EBV serology was positive. Differential diagnoses, including cutaneous lupus, leishmaniasis, and porphyria, were excluded. The patient was managed with strict photoprotection, leading to sustained remission over two years. Early diagnosis and sun protection are essential for managing HV, as seen in our case.

## Linked entities

- **Diseases:** Hydroa vacciniforme (MONDO:0018024), Epstein-Barr virus infection (MONDO:0005111), leishmaniasis (MONDO:0011989), porphyria (MONDO:0019142)

## Full-text entities

- **Genes:** NCAM1 (neural cell adhesion molecule 1) [NCBI Gene 4684] {aka CD56, MSK39, NCAM}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, GZMB (granzyme B) [NCBI Gene 3002] {aka C11, CCPI, CGL-1, CGL1, CSP-B, CSPB}, CD5 (CD5 molecule) [NCBI Gene 921] {aka LEU1, T1}, CD7 (CD7 molecule) [NCBI Gene 924] {aka GP40, LEU-9, TP41, Tp40}
- **Diseases:** porphyria (MESH:D011164), vesiculobullous facial lesions (MESH:D012872), EBV) infection (MESH:D020031), HV (MESH:D006837), hemorrhagic (MESH:D006470), leishmaniasis (MESH:D007896), cutaneous lupus (MESH:D008178)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12066078/full.md

## References

11 references — full list in the complete paper: https://tomesphere.com/paper/PMC12066078/full.md

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Source: https://tomesphere.com/paper/PMC12066078