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Bilateral Systematized Epidermolytic Verrucous Epidermal Nevus: A Rare Entity
Vivek Mishra1, Abanti Saha1, Debabrata Bandyopadhyay1
1Department of Dermatology, Venereology and Leprosy, Medical College, Kolkata, India.
This study presents a rare case of verrucous epidermal nevi in a 3-year-old boy. The condition presented as symmetrical plaques following Blaschko lines, with histopathology revealing prominent epidermolytic hyperkeratosis.
Area of Science:
- Dermatology
- Histopathology
- Genetics
Background:
- Verrucous epidermal nevi are congenital hamartomas of keratinocytes.
- They typically follow Blaschko lines and exhibit hyperkeratosis without atypia.
- Histological findings include hyperkeratosis, acanthosis, papillomatosis, and occasionally epidermolytic hyperkeratosis.
Purpose of the Study:
- To report a rare case of systematized verrucous epidermal nevi.
- To describe the clinical and histopathological features of this rare entity.
Main Methods:
- Case study of a 3-year-old boy.
- Clinical examination of skin lesions.
- Histopathological analysis of skin biopsy.
Main Results:
- The patient presented with bilaterally symmetrical, verrucous plaques along Blaschko lines on the trunk and extremities.
- Facial and palmoplantar skin were spared.
- Histopathology confirmed epidermal nevi with prominent epidermolytic hyperkeratosis.
Conclusions:
- This case highlights the rare presentation of systematized verrucous epidermal nevi.
- The prominent epidermolytic hyperkeratosis is a notable histopathological finding in this rare congenital condition.
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