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Oral lichen sclerosus expressing extracellular matrix proteins and IgG4-positive plasma cells

机译:口服地衣硬化剂表达细胞外基质蛋白和IgG4阳性血浆细胞

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Lichen sclerosus (LS) is a mucocutaneous disease with uncommon oral involvement. The etiology is not yet well understood, but LS has been associated with autoimmune, genetic, and immunological factors. We report a 47-year-old man with LS that exhibited an asymptomatic white plaque with red patches on the maxillary alveolar mucosa extending to the labial mucosa. He had no other skin disease. Positive immunostaining for tenascin and scarcity of fibronectin suggested extracellular matrix reorganization. Elastin immunostaining indicated a reduction of elastic fibers. Immunoexpression of collagen IV in blood vessels and its absence in the epithelial basement membrane, together with diffuse MMP-9 immunoexpression, suggested altered proteolytic activity. Mast cell staining bordering areas of sclerosis indicated a possible role in the synthesis of collagen. IgG4 positivity in plasma cells suggested a role in the fibrogenesis. This is an unusual presentation of oral LS and we discuss immunohistochemical findings regarding cellular and extracellular matrix components.
机译:Lichen Sclerosus(LS)是一种少数畸形的口服受累。该病因尚未充分理解,但LS与自身免疫,遗传和免疫因素有关。我们举报了一个47岁的男子,其中LS,在上颌肺泡粘膜上展出了一个无症状的白色斑块,延伸到阴唇粘膜。他没有其他皮肤病。对纤维蛋白的阳性免疫染色和纤连蛋白的稀缺性建议细胞外基质重组。弹性蛋白免疫染色表明弹性纤维的减少。血管中胶原素IV的免疫表达及其在上皮基底膜中的缺失以及弥漫性MMP-9免疫表达,提出了改变的蛋白水解活性。硬化症的肥大细胞染色区域表明了在合成胶原蛋白的可能作用。血浆细胞中的IgG4积极性表明在纤维发生中的作用。这是口腔LS的不寻常呈现,我们讨论了关于细胞和细胞外基质组分的免疫组织化学发现。

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