palmoplantar keratoderma

掌足底角化病
  • 文章类型: Randomized Controlled Trial
    我们研究了饮食海藻提取物硫酸化的木沙鼠葡糖醛酸(SXRG84)对患有炎性皮肤病的个体的影响。对一项更大的试验进行了亚组分析,其中44名患有皮肤疾病的参与者被纳入双盲安慰剂对照交叉设计。受试者摄入SXRG84提取物(2克/天)六周,安慰剂六周,反之亦然。在基线,评估了6周和12周的炎症标志物和肠道微生物群,以及使用皮肤病学生活质量指数(DQLI)进行的皮肤评估,银屑病面积严重度指数(PASI)和视觉模拟量表(VAS)。促炎细胞因子IFN-γ在第6周和第12周存在显着差异(p=0.041),IL-1β(p=0.030),TNF-α(p=0.008)和抗炎细胞因子IL-10(p=0.026),由ANCOVA确定。这些细胞因子均在安慰剂后6周显著高于随后SXRG84治疗的安慰剂后12周。共有23%的参与者报告皮肤改善,通过VAS(平均差3.1,p=0.0005)和DQLI评分(平均差-2.0,p=0.049)衡量,与“非响应者”相比。因此,摄入SXRG84持续6周可减少炎症细胞因子,一部分参与者看到了改进。
    We examined the effect of a dietary seaweed extract-sulfated xylorhamnoglucuronan (SXRG84)-on individuals with inflammatory skin conditions. A subgroup analysis of a larger trial was undertaken, where 44 participants with skin conditions were enrolled in a double-blind placebo-controlled crossover design. Subjects ingested either SXRG84 extract (2 g/day) for six weeks and placebo for six weeks, or vice versa. At baseline, six- and twelve-weeks inflammatory markers and the gut microbiota were assessed, as well as skin assessments using the dermatology quality of life index (DQLI), psoriasis area severity index (PASI) and visual analogue scales (VAS). There were significant differences at weeks six and twelve for pro-inflammatory cytokines IFN-γ (p = 0.041), IL-1β (p = 0.030), TNF-α (p = 0.008) and the anti-inflammatory cytokine IL-10 (p = 0.026), determined by ANCOVA. These cytokines were all significantly higher at six weeks post placebo compared to twelve weeks post placebo followed by SXRG84 treatment. A total of 23% of participants reported skin improvements, as measured by VAS (mean difference 3.1, p = 0.0005) and the DQLI score (mean difference -2.0, p = 0.049), compared to the \'non-responders\'. Thus, the ingestion of SXRG84 for 6 weeks reduced inflammatory cytokines, and a subset of participants saw improvements.
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  • 文章类型: Journal Article
    介绍掌plant皮肤病是特别影响手掌和鞋底的皮肤病,是皮肤科医生遇到的常见临床实体。这可能会给患者带来不适和尴尬,因为它的位置会严重干扰正常的日常活动。掌plant皮肤病会影响异质人群,从屠宰场的徒手工人到手术室戴着手套的医务人员。本研究试图根据掌足底皮肤病的形态和临床分布规律对掌足底皮肤病进行分类。材料和方法本研究是在奥斯曼尼亚总医院进行的为期六个月的描述性横断面研究,印度。共纳入80例符合研究纳入标准的掌足底皮肤病患者。在获得适当的知情同意后,数据来自患者的固定形式表.结果研究包括44例(55%)男性和36例(45%)女性患者。掌足底皮肤病的平均持续时间为2.92年。瘙痒和裂隙疼痛是患者抱怨的最常见症状,牛皮癣是32例(40%)患者中最常见的临床类型,其次是30例(37.5%)患者的湿疹和10例(12.5%)患者的真菌感染。结论术语掌plant皮肤病包括一组异质性的皮肤病,但没有确切的分类,并且类别根据要保留的疾病而有所不同。医生应充分了解这些皮肤病的临床特征,诊断对早期干预和正确处理非常重要,从而帮助提高患者的生活质量。
    Introduction Palmoplantar dermatoses are skin diseases affecting specifically palms and soles is a common clinical entity encountered by dermatologists. This may cause discomfort and embarrassment to the patients because its location interferes significantly with normal day-to-day activities. Palmoplantar dermatosis affects a heterogeneous population, ranging from bare-handed workers in the slaughterhouse to medical personnel wearing gloves in the operating room. The present study endeavors to classify palmoplantar dermatoses based on their morphology and the clinical distribution pattern. Materials and methods The present study is a descriptive cross-sectional study conducted for six months at Osmania General Hospital, India. A total number of 80 patients having palmoplantar dermatoses who met the study inclusion criteria were included. After taking proper informed consent, data were collected from patients on a fixed proforma sheet. Results The study comprised 44 (55%) male and 36 (45%) female patients. The mean duration of palmoplantar dermatoses was 2.92 years. Itching and painful fissures are the most common symptoms patients complained of and psoriasis is the most common clinical type seen in 32 (40%) patients followed by eczemas in 30 (37.5%) patients and fungal infections in 10 (12.5%) patients. Conclusion The term palmoplantar dermatoses includes a heterogeneous group of skin disorders but no exact classification is present and classes differ based on the diseases to be kept in a group. Physicians should be well aware of the clinical features of these dermatoses and diagnosis is very important for early intervention and correct management, thereby helping improve patients\' quality of life.
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  • 文章类型: Case Reports
    Papillon-Lefèvre syndrome (PLS) is a rare autosomal recessive disorder characterized by palmoplantar keratoderma and early-onset periodontitis. It was first described by Papillon and Lefèvre in 1924. PLS is caused by mutations in the cathepsin-C (CTSC) gene. The development of malignant skin neoplasms in PLS patients is extremely rare. To date, there have been two cases of malignant melanoma (MM) in PLS patients reported in international journals. Further, only one case of squamous cell carcinoma (SCC) has been reported in PLS patients. To the best of our knowledge, no cases with basal cell carcinoma in PLS patients have been reported in literature. Thus, we report a case of a 55-year-old male from Arabic Saudi with PLS and basal cell carcinoma. The patient was homozygous for a G-to-C substitution at the nucleotide position 815 (CTSC, c.815G>Cp.(Arg272Pro), which is a pathogenic variant. Since this is not the first case of skin cancer in PLS patients, we are supporting the possibility that cathepsin-C play a role in cancer development.
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