ArticleCureus2025
Extragenital Bullous Lichen Sclerosus in a Male Pediatric Patient and Dermoscopic Keys: A Case Report and Literature Review.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
4 authors.
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Abstract
We describe the case of a 12-year-old male who presented with a one-and-a-half-month history of an asymptomatic, rapidly expanding erythematous hyperkeratotic plaque on the left shoulder. On clinical exam, the patient was also found to have an ivory white atrophic plaque on the left clavicle. Given the classic lichen sclerosus (LS) lesion on the patient's clavicle, the lesion in question on his left shoulder was diagnosed as extragenital bullous LS (EBLS). The bullous variant of LS, while common in adult literature, is rarely reported in the pediatric population. The patient had a moderate clinical response to a high-potency topical corticosteroid. A review of this case, along with the literature, describes the epidemiology, clinical features, pathophysiology, and available treatment options for EBLS in the pediatric population.
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