Recent advances in palmoplantar pustulosis.

Faculty reviews Pub Date : 2021-07-27 eCollection Date: 2021-01-01 DOI:10.12703/r/10-62
Alexandra Maria Giovanna Brunasso, Cesare Massone
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引用次数: 17

Abstract

Palmoplantar pustulosis (PPP) is a chronic inflammatory condition where crops of sterile pustules with erythematous keratotic lesions causing bleeding and pain appear on the palms and soles. Recently, the European Rare and Severe Expert Network considered PPP as a variant of pustular psoriasis with or without psoriasis vulgaris. The prevalence of PPP varies from 0.050 to 0.12%. PPP occurs more frequently in women and the highest prevalence occurred between the ages of 50 and 69 years. Nail psoriasis seems to be frequent in PPP, ranging from 30 to 76%, and psoriatic arthritis in 8.6 to 26% of PPP patients. Synovitis, acne, pustulosis, hyperostosis, osteitis (SAPHO) syndrome and pustulotic arthro-osteitis are considered PPP-associated disorders. PPP has been reported with other co-morbidities such as psychiatric disorders, thyroid-associated disease, altered calcium homeostasis, gluten sensitivity diabetes, obesity, and dyslipidemia, but larger studies are required to prove such associations. Environmental exacerbating factors might contribute to the onset or worsening of PPP such as cigarette smoking, stress, focal infections, metal allergies, and drug intake. Genetic predisposition plays an important role in PPP. In PPP, both the innate and the adaptive immune systems are activated. The acrosyringeal expression of IL-17 has been demonstrated, indicating that the eccrine sweat gland is an active component of the skin barrier and an immune-competent structure. Increased levels of several inflammatory molecules, including IL-8, IL-1α, IL-1β, IL-17A, IL-17C, IL-17D, IL-17F, IL-22, IL-23A, and IL-23 receptor, have been detected in PPP biopsies. Increased serum levels of TNF-α, IL-17, IL-22, and IFN-γ have been detected in patients with PPP in comparison to healthy subjects, suggesting a similar inflammatory pattern to psoriasis vulgaris. Oral and tonsillar infections serve as trigger factors for PPP. Long-term therapy is required for many patients, but high-quality data are limited, contributing to uncertainty about the ideal approach to treatment.

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掌足底脓疱病的最新进展。
掌足底脓疱病(PPP)是一种慢性炎症性疾病,在手掌和脚底出现带有红斑性角化病变的无菌脓疱,引起出血和疼痛。最近,欧洲罕见和严重专家网络认为PPP是脓疱性牛皮癣的一种变体,伴或不伴寻常型牛皮癣。购买力平价的流行率从0.050到0.12%不等。PPP在女性中更为常见,发病率最高的年龄段为50至69岁。指甲牛皮癣似乎在PPP患者中很常见,从30%到76%不等,银屑病关节炎在PPP患者中占8.6到26%。滑膜炎、痤疮、脓疱病、骨质增生、骨炎(SAPHO)综合征和脓疱性关节-骨炎被认为是ppp相关疾病。据报道,PPP与其他合并症,如精神疾病、甲状腺相关疾病、钙稳态改变、麸质敏感性糖尿病、肥胖和血脂异常,但需要更大规模的研究来证明这些关联。环境恶化因素如吸烟、压力、局灶性感染、金属过敏和药物摄入等可能导致PPP的发生或恶化。遗传易感性在PPP中起重要作用。在PPP中,先天免疫系统和适应性免疫系统都被激活。IL-17在汗腺上的表达已被证实,这表明汗腺是皮肤屏障的活性成分和免疫活性结构。在PPP活检中检测到几种炎症分子水平升高,包括IL-8、IL-1α、IL-1β、IL-17A、IL-17C、IL-17D、IL-17F、IL-22、IL-23A和IL-23受体。与健康受试者相比,PPP患者血清中TNF-α、IL-17、IL-22和IFN-γ水平升高,提示其炎症模式与寻常型牛皮癣相似。口腔和扁桃体感染是PPP的触发因素。许多患者需要长期治疗,但高质量的数据有限,导致理想治疗方法的不确定性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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