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首页> 外文期刊>The Journal of dermatology >Clinical characteristics, genetics, comorbidities and treatment of palmoplantar pustulosis: A retrospective analysis of 66 cases in a single center in Taiwan
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Clinical characteristics, genetics, comorbidities and treatment of palmoplantar pustulosis: A retrospective analysis of 66 cases in a single center in Taiwan

机译:棕榈术脓疱病的临床特征,遗传学,综合性和治疗方法:台湾单一中心66例回顾性分析

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We retrospectively analyzed 66 patients with palmoplantar pustulosis (PPP) from January 1994 to September 2019 in our department. Interleukin-36 receptor antagonist gene (IL36RN) intron 3 c.115+6T>C mutation was present in two out of 27 patients (7.4%). Both cases developed generalized pustular psoriasis and/or acrodermatitis continua of Hallopeau later. Topical medications and phototherapy were used in 93.9% and 28.8% of patients, respectively, while 60.6% received systemic agents. The majority of patients (60.6%) responded to treatment, but episodes of flare-up existed. The demographic data of our patients with PPP showed female predominance (59.1%), middle-age onset (44.2 years old) and current smokers (62.1%). Generalized pustular psoriasis initially presenting as palmoplantar lesions may be misdiagnosed as PPP, and the presence ofIL36RNmutation may serve to predict or confirm the diagnosis of future generalized pustular psoriasis or acrodermatitis continua of Hallopeau. To our knowledge, this is the largest demographic study of PPP in Taiwan.
机译:我们回顾性分析了我科1994年1月至2019年9月的66例掌跖脓疱病(PPP)患者。27例患者中有2例(7.4%)出现白细胞介素36受体拮抗剂基因(IL36RN)内含子3 c.115+6T>c突变。这两个病例后来都发展为泛发性脓疱性银屑病和/或Hallopeau持续性肢端皮炎。分别有93.9%和28.8%的患者使用外用药物和光疗,60.6%的患者使用全身药物。大多数患者(60.6%)对治疗有反应,但仍有发作。我们的PPP患者的人口统计学数据显示,女性占优势(59.1%)、中年发病(44.2岁)和当前吸烟者(62.1%)。最初表现为掌跖病变的泛发性脓疱性银屑病可能被误诊为PPP,L36RN突变的存在可能有助于预测或确认未来泛发性脓疱性银屑病或Hallopeau持续性肢端皮炎的诊断。据我们所知,这是台湾最大的PPP人口统计研究。

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