Suppr超能文献

皮肤科中的斑蝥素

Cantharidin in Dermatology.

作者信息

Al-Dawsari Najla A, Masterpol Kasia Szyfelbein

机构信息

Department of Dermatology, John Hopkins Aramco Healthcare, Saudi Arabia;

Dermatology Associates, Winchester, MA.

出版信息

Skinmed. 2016 Apr 1;14(2):111-4. eCollection 2016.

Abstract

Cantharidin is natural toxin produced by the blistering beetle. It has both vesicant and keratolytic features by inducing acanthloysis through targeting the desmosomal dense plaque, leading to detachment of the desmosomes from the tonofilaments. There are two available liquid preparations for dermatologic use, Canthacur (0.7% cantharidin) and Canthacur PS (1% cantharidin 30%/salicylic acid/2% podophylotoxin). The former preparation is indicated for the treatment of common warts, periungual warts, and molluscum contagiosum, while the more potent latter preparation is indicated only for plantar warts. Both preparations provide painless applications with outcomes similar to other treatment modalities for warts and molluscum contagiosum; however, neither is approved by the Food and Drug Administration (FDA). The lack of FDA approval could be related to its toxic effects following oral ingestion, which include ulceration of the gastrointestinal and genitourinary tracts, along with electrolyte and renal function disturbance in humans and animals. The mechanism of action, dermatologic indications, application techniques, and complications of cantharidin preparations are discussed.

摘要

斑蝥素是一种由斑蝥甲虫产生的天然毒素。它具有发泡和角质溶解特性,通过靶向桥粒致密斑诱导棘层松解,导致桥粒与张力细丝分离。有两种用于皮肤科的液体制剂,Canthacur(0.7%斑蝥素)和Canthacur PS(1%斑蝥素/30%水杨酸/2%鬼臼毒素)。前一种制剂适用于治疗寻常疣、甲周疣和传染性软疣,而效力更强的后一种制剂仅适用于跖疣。两种制剂使用时均无痛,其治疗效果与其他治疗疣和传染性软疣的方法相似;然而,两种制剂均未获得美国食品药品监督管理局(FDA)的批准。缺乏FDA批准可能与其口服后的毒性作用有关,其毒性作用包括人和动物的胃肠道和泌尿生殖道溃疡,以及电解质和肾功能紊乱。本文讨论了斑蝥素制剂的作用机制、皮肤科适应症、应用技术和并发症。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验