Hashim S. Kaderbhai, Marlous L. Grijsen
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摘要

一名 23 岁的健康索马里妇女来到肯尼亚内罗毕的医院就诊,她的双前臂在一次传统婚礼上进行指甲花纹身 48 小时后出现了坚实的水泡(图 1 A、B)。两年前,她曾在一次指甲花纹身后出现过类似的症状,尽管症状较轻,但已自行消退。根据不同的病史和临床表现,她被诊断为对苯二胺(PPD)过敏性接触性皮炎。治疗包括外用皮质类固醇激素。对苯二胺(PPD)是一种强效致敏剂,常见于染发剂和纺织品染料中,而且越来越多地用于临时指甲花纹身,以延长纹身的寿命、加快干燥过程并增强着色效果[1]。患者再次接触 PPD 后引发了迟发型超敏反应。Henna是一种从Lawsonia inermis植物中提取的天然染料,是一种弱致敏剂。几个世纪以来,非洲、亚洲和中东地区一直将其用于药用和装饰目的,一般可持续 5-7 天[2]。含有 PPD 的长效临时指甲花纹身越来越受欢迎,这与皮肤过敏反应报告的增加有关[1]。有报告显示,指甲花纹身中的 PPD 浓度高得惊人,经常超过规定水平[3],进一步增加了过敏反应的风险。两位作者对最终稿件进行了审阅和批准,并同意发表。本手稿中的患者已提供书面知情同意书,同意将其去身份化的匿名数据和病例细节(包括照片)用于发表。伦理批准:不适用。作者声明无利益冲突。
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Allergic Contact Dermatitis to a Temporary Henna Tattoo

A 23-year-old healthy Somali woman presented at our hospital in Nairobi, Kenya, with firm blisters on both forearms that appeared 48 h after applying a henna tattoo for a traditional wedding (Figure 1 A,B). She had experienced similar, albeit milder, symptoms following a henna tattoo application 2 years prior, which had resolved spontaneously. The distinct history and clinical presentation led to the diagnosis of allergic contact dermatitis to para-phenylenediamine (PPD). Treatment involved topical corticosteroids. Epicutaneous patch testing was not available nor affordable in our setting.

PPD is a potent sensitizer commonly found in hair and textile dyes and is increasingly used in temporary henna tattoos to extend longevity, expedite the drying process and intensify the colouring [1]. The patient's re-exposure to PPD triggered a delayed-type hypersensitivity reaction. Henna is a natural dye derived from the Lawsonia inermis plant and is a weak sensitizer. It has been used for centuries in Africa, Asia and the Middle East for medicinal and decorative purposes and typically lasts 5−7 days [2]. The increasing popularity of long-lasting temporary henna tattoos containing PPD has been associated with an increase in reported allergic skin reactions [1]. Reports indicate that the concentration of PPD in henna tattoos is alarmingly high, often exceeding regulated levels [3], further elevating the risk of allergic reactions.

H.S.K. drafted the manuscript, and M.L.G. critically revised it. Both authors reviewed and approved the final manuscript and gave consent for publication.

The authors have nothing to report. The patient in this manuscript has provided written informed consent for the use of her deidentified anonymized data and her case details (including photographs) for publication. Ethical Approval: not applicable.

The authors declare no conflicts of interest.

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