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锌疗法治疗有症状的口腔扁平苔藓

Zinc Therapy in Treatment of Symptomatic Oral Lichen Planus.

作者信息

Chaitanya Nallan Csk, Chintada Suvarna, Kandi Pallavi, Kanikella Sushma, Kammari Anuja, Waghamare Rutuja S

机构信息

Department of Oral Medicine and Radiology, Panineeya Institute of Dental Sciences, Hyderabad, Telangana, India.

出版信息

Indian Dermatol Online J. 2019 Mar-Apr;10(2):174-177. doi: 10.4103/idoj.IDOJ_230_18.

Abstract

Lichen planus is a chronic inflammatory disease, which involves skin, mucous membrane, and nails. Prevalence of oral lichen planus varies between 0.5% and 2.6% of adult population worldwide with overall female preponderance. It is considered as a potentially malignant disorder with rate of transformation to oral cancer varying between 0.5% and 2%. Oral lichen planus may either be unilateral or bilateral, or may involve multiple sites. Although the exact etio-pathogenesis of this condition is unknown, it is believed that stress, use of medications, dental fillings, genetics, immunity, and hypersensitivity reactions may contribute to its pathogenesis. It is a T-cell-mediated autoimmune disorder in which CD8+ T cells are involved which release various cytokines such as tumor necrosis factor-α and interleuking-12 leading to disruption of basement membrane integrity. Zinc activates caspase-3 and DNA fragmentation, resulting in the apoptosis of keratinocytes. By prevention of matrix metalloproteinase (MMP)-1 activation, it inhibits T-cell accumulation in oral lichen planus, and by inhibiting MMP-9 it prevents cleavage of collagen IV resulting in maintaining the integrity of the basement membrane. The present case series describes the use of oral zinc acetate (50 mg) in patients having symptomatic oral lichen planus with favorable outcome in terms of size of lesion and global index score.

摘要

扁平苔藓是一种慢性炎症性疾病,累及皮肤、黏膜和指甲。全球成年人口中口腔扁平苔藓的患病率在0.5%至2.6%之间,总体上女性居多。它被认为是一种潜在的恶性疾病,转化为口腔癌的发生率在0.5%至2%之间。口腔扁平苔藓可以是单侧或双侧的,也可能累及多个部位。虽然这种疾病的确切病因发病机制尚不清楚,但人们认为压力、药物使用、补牙材料、遗传、免疫和过敏反应可能与其发病机制有关。它是一种T细胞介导的自身免疫性疾病,其中CD8 + T细胞参与其中,释放各种细胞因子,如肿瘤坏死因子-α和白细胞介素-12,导致基底膜完整性破坏。锌激活半胱天冬酶-3和DNA片段化,导致角质形成细胞凋亡。通过预防基质金属蛋白酶(MMP)-1的激活,它抑制口腔扁平苔藓中T细胞的积聚,并且通过抑制MMP-9,它防止IV型胶原的裂解,从而维持基底膜的完整性。本病例系列描述了口服醋酸锌(50毫克)在有症状的口腔扁平苔藓患者中的应用,在病变大小和总体指数评分方面取得了良好的效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c966/6434769/21019f9a3ac6/IDOJ-10-174-g001.jpg

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