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Lichen sclerosus and lichen planus: a spectrum of disease? Report of two cases and review of the literature.

机译:地衣硬皮病和扁平苔藓:疾病谱?两例报告并文献复习。

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摘要

There has long been controversy concerning the relationship between lichen planus and lichen sclerosus. Whilst these two conditions are now considered distinct, there are shared clinical and pathological features. We now describe two patients with the cutaneous involvement of both lichen planus and lichen sclerosus, presenting a review of similar reported cases and discussing the implications for pathogenesis of these two diseases. Neither lichen planus (LP) nor lichen sclerosus (LS) are uncommon yet they have only infrequently been reported as coexisting. In his original description of LS, however, Hallopeau considered it to be a variant of LP and Gougerot has also commented on a possible common pathogenesis for the two conditions. Features which tend to support such as association include the distribution of the cutaneous lesions, histopathological features such as hydropic basal cell degeneration and a band-like lymphohistiocytic infiltrate in the dermis, and the reported association with autoimmune disease. We now report two patients in whom coexistent cutaneous LS and LP was confirmed histologically.
机译:关于扁平苔藓和巩膜硬化之间的关系一直存在争议。尽管现在认为这两种情况是不同的,但它们具有共同的临床和病理特征。现在,我们描述了两名扁平苔藓和扁平苔藓皮肤受累的患者,介绍了类似报道的病例,并讨论了这两种疾病的发病机理。扁平苔藓(LP)和扁平苔藓(LS)都很少见,但很少有人报道它们共存。然而,在他对LS的最初描述中,Hallopeau认为它是LP的变体,而Gougerot也评论了这两种情况的可能的常见发病机理。趋于支持的特征例如关联包括皮肤病变的分布,组织病理学特征例如亲水性基底细胞变性和真皮中浸润的带状淋巴组织细胞,以及与自身免疫性疾病的报道关联。现在,我们报告了两名在组织学上证实皮肤LS和LP共存的患者。

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