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Bilateral zosteriform extragenital lichen sclerosus
This study reports a case of bilateral zosteriform extragenital lichen sclerosus (ELS) in a 35-year-old man. The diagnosis was confirmed through clinical examination and histopathology, highlighting ELS presentation along Blaschko lines.
Area of Science:
- Dermatology
- Pathology
Background:
- Extragenital lichen sclerosus (ELS) is a chronic inflammatory skin condition.
- ELS typically affects the genital area but can occur elsewhere.
- Zosteriform ELS, following Blaschko lines, is a rare presentation.
Observation:
- A 35-year-old man presented with asymptomatic, bilateral, linear eruptions on forearms and legs.
- Clinical examination revealed pearly white papules and depigmented atrophic plaques with telangiectasia.
- Lesions followed Blaschko lines, with sparing of genitalia, oral mucosa, palms, and soles.
Findings:
- Differential diagnoses included lichen striatus and ELS.
- Clinical features favored ELS.
- Histopathology confirmed lichen sclerosus with hyperkeratosis, epidermal atrophy, vacuolar degeneration, and dermal changes.
Implications:
- This case expands the understanding of ELS clinical presentations.
- Recognizing zosteriform ELS is crucial for accurate diagnosis and management.
- The findings emphasize the importance of histopathological correlation in diagnosing rare dermatoses.
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