A Pediatric Case of Erythrodermic Lichen Planus Pemphigoides

S. Maouni, El Anzi Ouiam, S. Asmae, Zenati Kaoutar, Meziane Mariam, Senouci Karima, Hassam Badredine
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引用次数: 2

Abstract

Lichen planus pemphigoides (LPP) is an uncommon skin condition that is characterized by signs of lichen planus associated to subepidermal detachment with deposits of autoantibodies along dermal-epidermal junction basement membrane. LPP is infrequent in adults, but extremely rare in pediatric population; indeed just 17 cases were reported. We report a rare case history of a 6-year-old boy with clinical and histological findings of an erythrodermic LPP.
儿童红皮病扁平地衣类天疱疮1例
类天疱疮扁平苔藓(LPP)是一种罕见的皮肤病,其特征是与表皮下脱离相关的扁平苔藓体征,并伴有真皮-表皮交界处基底膜上自身抗体的沉积。LPP在成人中罕见,但在儿科人群中极为罕见;事实上,仅报告了17例病例。我们报告一个罕见的病例历史的6岁男孩与临床和组织学发现的红皮病LPP。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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