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1例与西地那非柠檬酸盐相关的苔藓样药疹。

A case of lichenoid drug eruption associated with sildenafil citratus.

作者信息

Antiga Emiliano, Melani Lucilla, Cardinali Carla, Giomi Barbara, Caproni Marzia, Francalanci Stefano, Fabbri Paolo

机构信息

II Department of Dermatological Sciences, University of Florence, Italy.

出版信息

J Dermatol. 2005 Dec;32(12):972-5. doi: 10.1111/j.1346-8138.2005.tb00884.x.

Abstract

A 53-year-old man developed lichenoid lesions on the upper chest, posterior surfaces of the trunk, and abdominal region about three months before his first visit. Physical examination and laboratory findings were normal; histopathology showed vacuolar degeneration of basal keratinocytes in association with a dense lympho-histioid infiltrate arranged in a lichenoid pattern with a few melanophages and eosinophils. The fact that our patient had been irregularly taking sildenafil citratus (Viagra) led to the hypothesis of a lichenoid drug-induced eruption. Our hypothesis was confirmed by clinical resolution three weeks after discontinuation of sildenafil citratus; moreover, the patient avoided the drug for about four months, and the eruption didn't reappear. Subsequently, we performed a challenge test with the drug, and the patient developed similar lichenoid lesions. Lichenoid eruptions are rather common dermatoses that can be induced by a great number of environmental agents and are clinically but not pathogenetically well defined. We report the present case because, despite the great number of drugs that can be implicated in the development of lichenoid eruptions, the association of such dermatoses and sildenafil citratus had been described only once previously in the literature until now. Furthermore, we wish to remark on the significance of a detailed anamnestic history to make the correct differential diagnosis between lichenoid drug-induced eruptions and lichen planus. This has a great clinical importance because simple discontinuation or substitution of the drug causes lichenoid drug-induced eruption resolution.

摘要

一名53岁男性在首次就诊前约三个月,胸部上方、躯干后表面及腹部出现苔藓样病变。体格检查和实验室检查结果均正常;组织病理学显示基底角质形成细胞空泡变性,伴有呈苔藓样排列的密集淋巴组织细胞浸润,可见少量噬黑素细胞和嗜酸性粒细胞。该患者一直在不规则服用西地那非(万艾可),这使得我们推测该苔藓样皮疹为药物性皮疹。停用西地那非三周后临床症状消退,证实了我们的推测;此外,患者停用该药约四个月,皮疹未再出现。随后,我们对该药物进行了激发试验,患者再次出现了类似的苔藓样病变。苔藓样疹是一种相当常见的皮肤病,可由多种环境因素诱发,临床特征明确但发病机制尚不明确。我们报告该病例是因为,尽管有大量药物可引发苔藓样疹,但截至目前,这种皮肤病与西地那非的关联在文献中仅被描述过一次。此外,我们想强调详细的既往史对于正确鉴别药物性苔藓样疹和扁平苔藓的重要性。这具有重要的临床意义,因为简单停用或更换药物即可使药物性苔藓样疹消退。

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