{Reference Type}: Case Reports
{Title}: Exclusive extragenital lichen sclerosis in a child presenting in a lichen planus distribution.
{Author}: Murshidi R;AlSamhori JF;AlSamhouri ARF;Hamad SB;Abdaljaleel M;AlShammas F;
{Journal}: Dermatol Online J
{Volume}: 30
{Issue}: 3
{Year}: 2024 Jun 15
暂无{DOI}: 10.5070/D330363865
{Abstract}: Lichen sclerosus (LS) is a chronic inflammatory dermatosis primarily affecting the genitalia, commonly characterized by pearly-white papules and plaques. Although predominantly affecting females, LS can manifest across all age groups, with a bimodal distribution observed in prepubescent girls and postmenopausal women. This case report presents an unusual instance of exclusive extragenital LS in a 10-year-old girl, showcasing hyperpigmented patches and wrinkled plaques resembling lichen planus on her forearms and lower legs. Histopathological analysis confirmed LS, revealing distinctive epidermal changes and lymphocytic infiltrates. The absence of mucosal involvement and unique clinical presentation differentiated this case from typical LS manifestations. Treatment with topical clobetasol propionate demonstrated significant improvement in pruritus. Extragenital LS is infrequent, particularly among children, and its diagnosis necessitates a comprehensive clinicopathological correlation. The reported case contributes valuable insights into this uncommon variant, emphasizing the importance of accurate diagnosis and tailored treatment strategies. Additionally, it highlights the efficacy of high-potency topical corticosteroids in managing this condition.