Verrucous epidermal nevus with epidermolytic hyperkeratosis: Histopathological-dermoscopic correlation

Dear Sir, Verrucous epidermal nevi (VEN) are non-inflammatory hamartomatous growths composed of keratinocytes.[1] ey present as velvety, skin-colored to dark brown papules and plaques, appearing along the Blaschko lines.[2] Epidermolytic hyperkeratotic epidermal nevus (EN) is a rare variant showing cutaneous mosaicism.[3] Epidermolytic EN may present at birth, though it may appear as late as adulthood.[4] is variant is classically caused by mutations in the KRT1 and KRT10 genes.[3] While VEN may have a mutation in the FGFR3 gene, the same gene which is responsible for the development of seborrheic keratosis (SK).[2] Dermoscopy of epidermolytic EN shows features similar to those of any other EN, but it can resemble that of SK because of their morphologic similarity.We present a case of epidermolytic VEN with SK-like dermoscopic features.

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Publication Details

Journal
Cosmoderma
Published
2026-08-27
DOI
https://doi.org/10.25259/csdm_153_2026
Primary Topic
Genetic and rare skin diseases.
Type
article
Field-Weighted Citation Impact
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article

Verrucous epidermal nevus with epidermolytic hyperkeratosis: Histopathological-dermoscopic correlation

Sadhana Raturi, Pritika Nehra
Cosmoderma
Genetic and rare skin diseases.
article

Verrucous epidermal nevus with epidermolytic hyperkeratosis: Histopathological-dermoscopic correlation

Sadhana Raturi, Pritika Nehra
article en

Abstract

Dear Sir, Verrucous epidermal nevi (VEN) are non-inflammatory hamartomatous growths composed of keratinocytes.[1] ey present as velvety, skin-colored to dark brown papules and plaques, appearing along the Blaschko lines.[2] Epidermolytic hyperkeratotic epidermal nevus (EN) is a rare variant showing cutaneous mosaicism.[3] Epidermolytic EN may present at birth, though it may appear as late as adulthood.[4] is variant is classically caused by mutations in the KRT1 and KRT10 genes.[3] While VEN may have a mutation in the FGFR3 gene, the same gene which is responsible for the development of seborrheic keratosis (SK).[2] Dermoscopy of epidermolytic EN shows features similar to those of any other EN, but it can resemble that of SK because of their morphologic similarity.We present a case of epidermolytic VEN with SK-like dermoscopic features.

CosmodermaVol. 6
Shri Maharaja Hari Singh Hospital (IN), National Institute of Technology Srinagar (IN), Dehradun Institute of Technology University (IN)
Openalex Percentile: Top 10%
Genetic and rare skin diseases.
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