# Unusual Presentation of Epidermodysplasia Verruciformis (EV) in Non-Sun Exposed Area: A Case Report

**Authors:** Nidal Jebrini, Majed Dwaik, Mohanad Jaber, Sami Jabari, Raghad Razem, Man Sarahna, Rashad Alzaro, Feras Aljabari, Mohamed Aqel, Husein Sarahneh

PMC · DOI: 10.1155/crdm/7801944 · Case Reports in Dermatological Medicine · 2025-03-26

## TL;DR

A rare case of skin cancer in a sun-protected area was found in a woman with a genetic skin condition called EV, challenging the usual understanding of where such cancers occur.

## Contribution

This is the second global case of SCC in a non-sun-exposed area among EV patients, challenging the sun-exposure paradigm.

## Key findings

- A 28-year-old woman with EV developed SCC on her scalp, a non-sun-exposed area.
- The patient had multiple lesions resembling trichoblastic and verrucous carcinoma.
- This case highlights the need for close monitoring and UV protection in EV patients.

## Abstract

Introduction and Importance: Epidermodysplasia verruciformis (EV), a rare hereditary skin disorder linked to HPV immunity, increases the risk of squamous cell carcinoma (SCC), typically in sun-exposed areas. This case highlights an extraordinary instance of SCC in a Sun-shielded region, marking the second documented case globally.

Methods: The medical records and histopathological slides of the case were retrospectively reviewed. This work has been reported based on the CARE criteria.

Case Presentation: A 28-year-old Palestinian woman, who adheres to a sun-protective Hijab due to her Muslim faith and has limited sun exposure working in a clothing store, with painful scalp lesions presented at the dermatology clinic. She and her siblings were diagnosed with EV. Three years ago, a painful, enlarging lesion on her scalp led to a diagnosis of trichoblastic carcinoma, followed by the development of six similar lesions. A year later, she returned with multiple painful, pus-producing lesions exhibiting features of trichoblastic and verrucous carcinoma, posing a challenging clinical scenario.

Clinical Discussion: EV is a rare genetic skin disorder linked to EVER1/TCM6 or EVER2/TCM8 gene mutations, causing widespread warts due to specific HPV types. It heightens the risk of nonmelanoma skin cancer (NMSC), mainly SCC, often associated with beta-HPVs 5 and 8. Notably, atypical cases challenge the sun-exposure SCC concept. The reatment involves UV protection, retinoids, and close monitoring, critical to prevent lesion recurrence and aggressive malignancy interventions upon therapy discontinuation.

Conclusion: In this unique case, a patient with EV developed SCC in an uncommonly sun-protected skin area, highlighting the extreme rarity of such an event within the context of this condition's complications.

## Linked entities

- **Diseases:** Epidermodysplasia verruciformis (MONDO:0009176), squamous cell carcinoma (MONDO:0005096), verrucous carcinoma (MONDO:0006006), nonmelanoma skin cancer (MONDO:0002656)

## Full-text entities

- **Genes:** TMC6 (transmembrane channel like 6) [NCBI Gene 11322] {aka EV1, EVER1, EVIN1, LAK-4P, TNRC6C-AS1, lnc}, TMC8 (transmembrane channel like 8) [NCBI Gene 147138] {aka EV2, EVER2, EVIN2}
- **Diseases:** trichoblastic and verrucous carcinoma (MESH:D018289), warts (MESH:D014860), malignancy (MESH:D009369), scalp lesions (MESH:D004476), hereditary skin disorder (MESH:D009386), NMSC (MESH:D012878), EV (MESH:D004819), SCC (MESH:D002294), skin disorder (MESH:D012871)
- **Chemicals:** retinoids (MESH:D012176)
- **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/PMC11964711/full.md

## References

12 references — full list in the complete paper: https://tomesphere.com/paper/PMC11964711/full.md

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Source: https://tomesphere.com/paper/PMC11964711