Clinical, Cosmetic and Investigational Dermatology最新文献

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Anti-MDA5 Positive Dermatomyositis Overlapping with Rheumatoid Arthritis: A Case Report. 抗mda5阳性皮肌炎合并类风湿关节炎1例
IF 2.2 4区 医学
Clinical, Cosmetic and Investigational Dermatology Pub Date : 2025-09-15 eCollection Date: 2025-01-01 DOI: 10.2147/CCID.S537273
Fuzhen Yuan, Zhenhua Huang, Eryao Zhang, Dingye Yao, Junsheng Sun
{"title":"Anti-MDA5 Positive Dermatomyositis Overlapping with Rheumatoid Arthritis: A Case Report.","authors":"Fuzhen Yuan, Zhenhua Huang, Eryao Zhang, Dingye Yao, Junsheng Sun","doi":"10.2147/CCID.S537273","DOIUrl":"10.2147/CCID.S537273","url":null,"abstract":"<p><p>We report a rare case of overlap syndrome between anti-MDA5-positive dermatomyositis (DM) and rheumatoid arthritis (RA) in a 65-year-old woman. Initially diagnosed with RA, the patient later developed characteristic DM manifestations including characteristic DM rash, generalized weakness, poor appetite, and unintentional weight loss. Laboratory findings revealed elevated muscle enzymes, positive anti-melanoma differentiation-associated gene 5 (MDA5) antibody and anti-Ro52 antibodies, and increased anti-citrullinated protein antibodies. The patient showed significant improvement following combination therapy with prednisone and mycophenolate mofetil, highlighting the importance of early recognition and appropriate management of this rare overlap syndrome.</p>","PeriodicalId":10447,"journal":{"name":"Clinical, Cosmetic and Investigational Dermatology","volume":"18 ","pages":"2371-2376"},"PeriodicalIF":2.2,"publicationDate":"2025-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12447974/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145112212","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Successful Treatment of Childhood Nail Lichen Planus with Ruxolitinib Cream: A Case Report. 鲁索利替尼乳膏治疗小儿甲扁平苔藓1例。
IF 2.2 4区 医学
Clinical, Cosmetic and Investigational Dermatology Pub Date : 2025-09-14 eCollection Date: 2025-01-01 DOI: 10.2147/CCID.S542446
Anqi Sheng, Wenting Hu, Ai'e Xu
{"title":"Successful Treatment of Childhood Nail Lichen Planus with Ruxolitinib Cream: A Case Report.","authors":"Anqi Sheng, Wenting Hu, Ai'e Xu","doi":"10.2147/CCID.S542446","DOIUrl":"10.2147/CCID.S542446","url":null,"abstract":"<p><p>The role of oral JAK inhibitors in the treatment of nail lichen planus (NLP) has recently been reported, but there have been no literature reports on the treatment of NLP with topical Janus kinase (JAK) inhibitor. We present, for the first time, a preliminary clinical experience with topical ruxolitinib cream, a JAK inhibitor, in a child with NLP. The remarkable results suggest topical ruxolitinib cream may be a potential treatment option for NLP.</p>","PeriodicalId":10447,"journal":{"name":"Clinical, Cosmetic and Investigational Dermatology","volume":"18 ","pages":"2367-2370"},"PeriodicalIF":2.2,"publicationDate":"2025-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12445295/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145112183","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Tape-Strip Proteomic Analysis of Female Melasma Skin Lesions in a Chinese Population. 中国女性黄褐斑皮肤病变的条带蛋白质组学分析。
IF 2.2 4区 医学
Clinical, Cosmetic and Investigational Dermatology Pub Date : 2025-09-12 eCollection Date: 2025-01-01 DOI: 10.2147/CCID.S538073
Yi Yang, Zheng Zhao, Lulu Lu, Na Gao, Jiangang Hu, Gangwen Han, Xiaolei Ma
{"title":"Tape-Strip Proteomic Analysis of Female Melasma Skin Lesions in a Chinese Population.","authors":"Yi Yang, Zheng Zhao, Lulu Lu, Na Gao, Jiangang Hu, Gangwen Han, Xiaolei Ma","doi":"10.2147/CCID.S538073","DOIUrl":"10.2147/CCID.S538073","url":null,"abstract":"<p><strong>Purpose: </strong>Melasma is a common, chronic, and recurring disorder of hyperpigmentation arising from hyperfunctional melanocytes that deposit excessive amounts of melanin in the epidermis and dermis. The pathophysiology of melasma remains unclear and the treatment is challenging. Proteomic Analysis may contribute to understand the pathogenesis of melasma.</p><p><strong>Patients and methods: </strong>In this study, transepidermal water loss(TWEL) was evaluated to assess skin barrier function. Melasma area and severity index score was used to measure the severity of melasma. Data independent acquisition mass spectrometry was used to perform a comparative analysis of protein expression in female skin samples(cheeks) from 8 healthy controls and 8 melasma subjects. The hospital anxiety and depression scale were used to assess the anxiety and depression levels of the melasma patients.</p><p><strong>Results: </strong>The results showed that the melasma patients had higher TEWL values than the controls (12.95 ± 2.44 versus 6.86 ± 2.19, p < 0.01). Quantitative proteomic analysis identified a total of 230 differentially expressed proteins, including 193 upregulated and 37 downregulated. Enrichment analysis of these proteins based on GO, KEGG databases and protein-protein interaction analysis revealed that functional cluster associated with skin barrier (which included ALB, ANXA5, HSPB1, IQGAP1, S100A7), immunity and inflammation (which included YWHAZ, YWHAE, HSPA5, CSNK2B), melanogenesis (which included ALDH1A1, YWHAH, NDRG2, PMEL, APOE), psychoneurosis (which included YWHAE,YWHAH, PFN1, C3) and hormone (which included ARPC2, HSC70 and HSP70).</p><p><strong>Conclusion: </strong>Our non-invasive proteomics analysis of human epidermal proteins may guide future research on female melasma and help in the development of treatments for melasma.</p>","PeriodicalId":10447,"journal":{"name":"Clinical, Cosmetic and Investigational Dermatology","volume":"18 ","pages":"2341-2357"},"PeriodicalIF":2.2,"publicationDate":"2025-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12439839/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145079843","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effect of Methotrexate Discontinuation on Psoriatic Patients with Significant Liver Fibrosis. 甲氨蝶呤停药对银屑病肝纤维化患者的影响。
IF 2.2 4区 医学
Clinical, Cosmetic and Investigational Dermatology Pub Date : 2025-09-12 eCollection Date: 2025-01-01 DOI: 10.2147/CCID.S547056
Tanat Yongpisarn, Kunlawat Thadanipon, Ploysyne Rattanakaemakorn
{"title":"Effect of Methotrexate Discontinuation on Psoriatic Patients with Significant Liver Fibrosis.","authors":"Tanat Yongpisarn, Kunlawat Thadanipon, Ploysyne Rattanakaemakorn","doi":"10.2147/CCID.S547056","DOIUrl":"10.2147/CCID.S547056","url":null,"abstract":"<p><strong>Background: </strong>Patients with psoriasis, particularly those receiving systemic therapies such as methotrexate (MTX), are at increased risk of developing significant liver fibrosis. Although MTX remains widely used, its hepatotoxic potential remains controversial. Transient elastography (TE) allows non-invasive monitoring of liver fibrosis; however, data on fibrosis regression after MTX discontinuation are limited.</p><p><strong>Objective: </strong>To assess the incidence of liver fibrosis regression in psoriasis patients following MTX withdrawal and to identify clinical and laboratory factors associated with this outcome.</p><p><strong>Methods: </strong>We conducted a pilot cross-sectional study involving 15 prospectively recruited psoriasis patients with significant liver fibrosis (liver stiffness measurement [LSM] ≥7.1 kPa) who had discontinued MTX for at least 6 months. Fibrosis regression was defined as a >30% reduction in LSM from baseline. Univariate logistic regression was used to evaluate associations between clinical variables and fibrosis regression.</p><p><strong>Results: </strong>Fibrosis regression was observed in 5 patients (33.3%) who had remained MTX-free for a mean duration of 3.6 ± 3.1 years. MTX treatment duration >4 years was significantly associated with fibrosis regression (OR = 16.00, 95% CI: 1.09-234.25; p = 0.043). A cumulative MTX dose >2 grams showed a non-significant trend toward increased odds of fibrosis regression (OR = 6.00, 95% CI: 0.56-63.98; p = 0.138). Male gender (OR = 0.17, 95% CI: 0.02-1.78; p = 0.138) showed a non-significant trend toward reduced odds of fibrosis regression.</p><p><strong>Conclusion: </strong>One-third of psoriasis patients with significant liver fibrosis showed regression after a mean MTX-free duration of 3.6 years, with MTX use duration of more than 4 years significantly associated with this outcome. Given the small sample size, these results should be interpreted with caution. Nonetheless, these findings suggest a potential benefit of MTX withdrawal in selected patients and warrant confirmation in larger, prospective studies.</p>","PeriodicalId":10447,"journal":{"name":"Clinical, Cosmetic and Investigational Dermatology","volume":"18 ","pages":"2315-2321"},"PeriodicalIF":2.2,"publicationDate":"2025-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12439842/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145079795","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The Anti-Aging Effects of Adipose-Derived Mesenchymal Stem Cell Exosomes on Skin and Their Potential for Personalized Skincare Applications. 脂肪来源的间充质干细胞外泌体对皮肤的抗衰老作用及其在个性化护肤应用中的潜力。
IF 2.2 4区 医学
Clinical, Cosmetic and Investigational Dermatology Pub Date : 2025-09-12 eCollection Date: 2025-01-01 DOI: 10.2147/CCID.S547675
Yan-Xiu Jin, Guang-Zhen Jin
{"title":"The Anti-Aging Effects of Adipose-Derived Mesenchymal Stem Cell Exosomes on Skin and Their Potential for Personalized Skincare Applications.","authors":"Yan-Xiu Jin, Guang-Zhen Jin","doi":"10.2147/CCID.S547675","DOIUrl":"10.2147/CCID.S547675","url":null,"abstract":"<p><p>Stem cell-derive exosomes have gained increasing attention in the skincare industry in recent years due to their multiple anti-aging benefits. However, differences in cell sources lead to significant heterogeneity in the composition of secreted exosomes, resulting in inconsistent biological effects. Moreover, the lack of standardized production protocols and the technical challenges associated with large-scale manufacturing continue to limit their broader application in the beauty industry. As a narrative review, this article systematically summarizes the biological functions and mechanisms of action of autologous adipose mesenchymal stem cell-derived exosomes (AMSCs-Exos) in anti-skin aging, covering in vitro, in vivo, and clinical studies. Recent studies have shown that autologous exosomes derived from AMSCs not only possess the common bioactivity shared by stem cell-derived exosomes but also exhibit higher biocompatibility and a lower risk of pathogen transmission. In addition, their suitability for small-scale production makes them a more advantageous option. Furthermore, advances in artificial intelligence (AI) technology are driving the transformation of the cosmetics industry from traditional skincare to personalized skincare: AI provides a basis for the personalized matching of exosome dosage and delivery methods through high-precision skin condition monitoring. It optimizes the iteration of customized exosome products by integrating intelligent analysis of dynamic changes in users' skin texture and usage feedback, and achieves closed-loop management from \"universal formulations\" to \"precision repair\" by combining skin physiological data with user preferences. The integration of AI with AMSCs-Exos not only expands their potential in personalized skincare applications but also holds promise for generating valuable clinical data, thereby further advancing the concept and scientific development of precision skincare.</p>","PeriodicalId":10447,"journal":{"name":"Clinical, Cosmetic and Investigational Dermatology","volume":"18 ","pages":"2267-2284"},"PeriodicalIF":2.2,"publicationDate":"2025-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12439826/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145079800","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
No Causal Relationship Between Helicobacter Pylori Infection and Rosacea: A 2-Sample Mendelian Randomization Study. 幽门螺杆菌感染与酒渣鼻无因果关系:一项两样本孟德尔随机研究。
IF 2.2 4区 医学
Clinical, Cosmetic and Investigational Dermatology Pub Date : 2025-09-12 eCollection Date: 2025-01-01 DOI: 10.2147/CCID.S543236
Yu Qiu, Sihao Shen, Yong Zhang
{"title":"No Causal Relationship Between Helicobacter Pylori Infection and Rosacea: A 2-Sample Mendelian Randomization Study.","authors":"Yu Qiu, Sihao Shen, Yong Zhang","doi":"10.2147/CCID.S543236","DOIUrl":"10.2147/CCID.S543236","url":null,"abstract":"<p><strong>Background: </strong>Previous studies have shown that patients with rosacea have a higher prevalence of Helicobacter pylori (H. pylori) infection. However, whether H. pylori infection contributes to the development of rosacea remains unclear, and no genetic association studies between the two have been conducted to date. Genome-wide association studies (GWAS) database is a public resource that stores and shares data that aims to identify genetic links to complex diseases, physiological traits, or drug responses. Mendelian randomization (MR) is an epidemiological approach to investigate the effect of the exposure on a specific outcome. Due to the random assortment of single nucleotide polymorphisms (SNPs), they are less likely to be influenced by confounding factors. The MR design can mitigate residual confounding and reverse causation, strengthening the causal inference of the exposure's association with the outcome.</p><p><strong>Methods: </strong>We use GWAS database and MR design to assess the causal relationship between H. pylori infection and rosacea. Inverse variance weighted (IVW) was the main method in this study, along with MR Egger, simple mode, weighted median, and weighted mode. GWAS data for H. pylori infection and rosacea were retrieved from the Medical Research Council Integrative Epidemiology Unit (MRC-IEU) Open GWAS, GWAS catalog and FinnGen database.</p><p><strong>Results: </strong>We used H. pylori infection as exposure data and rosacea as outcome data, and all p-values in MR analysis were all greater than 0.05. These conclusions were confirmed by sensitivity analysis.</p><p><strong>Conclusion: </strong>Our MR analysis provides no evidence of a causal relationship between H. pylori infection and rosacea. This indicates that patients with rosacea may not need routine testing for H. pylori infection and routine eradication of H. pylori may not benefit rosacea patients.</p>","PeriodicalId":10447,"journal":{"name":"Clinical, Cosmetic and Investigational Dermatology","volume":"18 ","pages":"2359-2365"},"PeriodicalIF":2.2,"publicationDate":"2025-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12439818/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145079774","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Integrated Single-Cell and Spatial Transcriptomic Analysis Reveals a Pathological Niche Formed by FAP+ Fibroblasts, Immune, and Endothelial Cells in Psoriatic Lesions. 综合单细胞和空间转录组学分析揭示了银屑病病变中FAP+成纤维细胞、免疫细胞和内皮细胞形成的病理生态位。
IF 2.2 4区 医学
Clinical, Cosmetic and Investigational Dermatology Pub Date : 2025-09-12 eCollection Date: 2025-01-01 DOI: 10.2147/CCID.S541106
Wuwei Zhuang, Qi Zhang, Qingtao Kong, Yun Hui, Jie Shen, Chen Zhang, Hong Sang, Qiao Ye
{"title":"Integrated Single-Cell and Spatial Transcriptomic Analysis Reveals a Pathological Niche Formed by FAP+ Fibroblasts, Immune, and Endothelial Cells in Psoriatic Lesions.","authors":"Wuwei Zhuang, Qi Zhang, Qingtao Kong, Yun Hui, Jie Shen, Chen Zhang, Hong Sang, Qiao Ye","doi":"10.2147/CCID.S541106","DOIUrl":"10.2147/CCID.S541106","url":null,"abstract":"<p><strong>Purpose: </strong>The dysregulated immune microenvironment represents a key pathogenic driver in psoriatic lesions. However, the intricate cellular and molecular interactions underlying psoriasis remain incompletely elucidated. Therefore, we aim to employ integrated multi-omics approaches to characterize the immune microenvironment and pathogenic niche in psoriasis, thereby elucidating the cellular and molecular mechanisms of disease pathogenesis.</p><p><strong>Methods: </strong>Integrated Single-cell RNA sequencing (scRNA-seq), spatial transcriptomics, and bulk RNA sequencing (RNA-seq) data to explore the heterogeneity of stromal cells and immune cells in psoriatic lesions and the complex spatial niches formed between them. Enrichment analysis, intercellular communication analysis, and spatial co-localization analysis were used to investigate the transcriptional changes and distribution characteristics of each cell type in the lesions of psoriasis patients.</p><p><strong>Results: </strong>Using scRNA-seq, we identified a novel CD4+ tissue-resident memory T cell (TRM) subset that is exclusively present in lesional skin of psoriasis patients but absent in healthy skin. These cells exhibit elevated expression of genes including IL17RA, IL22, PD1 (PDCD1), CXCR6, ITGAE, CD69, TNFRSF9, TNFRSF4, IL7R, CD4, and STAT3. Additionally, we discovered a novel microvascular endothelial cell subset, designated Venous endo2, which highly expresses CD93, ACKR1, ICAM1, VCAM1, IL15, SELE, and SELP, while also overlapping with high endothelial venule (HEV)-associated transcriptional signatures. Integrated analysis of scRNA-seq and spatial transcriptomics further revealed strong spatial co-localization of Venous endo2 with fibroblast activation protein-positive fibroblasts (FAP+ Fbs), T cells, and antigen-presenting cells (APCs) in Psoriasis lesions-a pattern not observed in healthy control skin.</p><p><strong>Conclusion: </strong>Through integrated multi-omics analysis, we identified a potential pathogenic niche in psoriasis patients, composed of Venous endo2, FAP+ Fbs, T cells, and APCs. This structure resembles tertiary lymphoid structures (TLS), suggesting a functional parallel in disease pathogenesis.</p>","PeriodicalId":10447,"journal":{"name":"Clinical, Cosmetic and Investigational Dermatology","volume":"18 ","pages":"2323-2340"},"PeriodicalIF":2.2,"publicationDate":"2025-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12439697/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145079838","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Comprehensive Review of Predictive Precision in Scar Medicine: From Molecular Predictors to Machine Learning Models. 疤痕医学预测精度综述:从分子预测器到机器学习模型。
IF 2.2 4区 医学
Clinical, Cosmetic and Investigational Dermatology Pub Date : 2025-09-11 eCollection Date: 2025-01-01 DOI: 10.2147/CCID.S542866
Jinzhao Su, Jingbin Chen, Tianrong Wang, Tiansheng Lin
{"title":"A Comprehensive Review of Predictive Precision in Scar Medicine: From Molecular Predictors to Machine Learning Models.","authors":"Jinzhao Su, Jingbin Chen, Tianrong Wang, Tiansheng Lin","doi":"10.2147/CCID.S542866","DOIUrl":"10.2147/CCID.S542866","url":null,"abstract":"<p><p>Scars-including keloids, hypertrophic scars, and acne scars-pose substantial functional and psychosocial burdens that current empirical treatments often address by trial-and-error. Quantitative evidence now supports a precision framework. Validated clinical tools (eg, VSS, POSAS) and imaging modalities (3D photogrammetry; high-frequency ultrasound elastography) provide objective baselines, while emerging AI models deliver measurable gains: an automated scar-type classifier achieved precision 80.7%, recall 71.0%, AUC 0.846 for image-based categorization, and a clinical recurrence model for keloids reported AUC 0.889 with sensitivity 78.7% and specificity 86.8%, enabling earlier risk-stratified interventions and fewer ineffective treatment cycles in model-informed pathways. We synthesize cytokine/fibroblast signatures and genetic predisposition with multimodal (clinical-imaging-molecular) learning, detail validation challenges, and propose actionable safeguards (TRIPOD+AI-aligned reporting, internal-external validation, bias audits, SHAP-based interpretability, and federated learning to preserve privacy and improve generalizability). A pragmatic roadmap-including funding mechanisms, stakeholder roles, and a barrier-solution matrix-aims to accelerate translation toward predictive, preventive, and personalized scar care.</p>","PeriodicalId":10447,"journal":{"name":"Clinical, Cosmetic and Investigational Dermatology","volume":"18 ","pages":"2303-2314"},"PeriodicalIF":2.2,"publicationDate":"2025-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12435524/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145074350","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The Hidden Epidemic of Topical Steroid Use: Prevalence and Impact Among Jordan's General Population. 局部类固醇使用的隐藏流行病:约旦普通人群的流行和影响。
IF 2.2 4区 医学
Clinical, Cosmetic and Investigational Dermatology Pub Date : 2025-09-11 eCollection Date: 2025-01-01 DOI: 10.2147/CCID.S553615
Hanadi Qeyam, Rola Al-Shaimi, Noor Abed Alfattah, Ensaf Y Almomani, Ahmed Al-Rusan, Jihan Muhaidat, Diala Alshiyab, Firas Al-Qarqaz, Leen Heis
{"title":"The Hidden Epidemic of Topical Steroid Use: Prevalence and Impact Among Jordan's General Population.","authors":"Hanadi Qeyam, Rola Al-Shaimi, Noor Abed Alfattah, Ensaf Y Almomani, Ahmed Al-Rusan, Jihan Muhaidat, Diala Alshiyab, Firas Al-Qarqaz, Leen Heis","doi":"10.2147/CCID.S553615","DOIUrl":"10.2147/CCID.S553615","url":null,"abstract":"<p><strong>Background: </strong>Topical corticosteroids (TCS) are widely prescribed for inflammatory skin conditions, but unsupervised use carries significant health risks. In Jordan, over-the-counter availability raises concerns about misuse. Limited research exists on population-level patterns and knowledge. This study aimed to evaluate TCS use patterns, indications, and awareness in the general population, and to identify demographic factors associated with misuse.</p><p><strong>Methods: </strong>A cross-sectional online survey was distributed via social media platforms. The questionnaire assessed demographics, corticosteroid use patterns, application sites, prescription sources, and awareness of products and side effects. Data were analyzed using Jamovi (version 2.3.28). Descriptive statistics were generated, and chi-square tests and multiple linear regression were used to identify associations with cream recognition and adverse effect reporting.</p><p><strong>Results: </strong>A total of 714 respondents participated; 46.8% reported storing corticosteroid creams at home. The most common application sites were the hands (36.6%) and face (31.2%). Daily use was most frequent (53.1%). Creams were mainly obtained from pharmacists (22.8%) or informal sources (12.6%). Only 63.2% reported reading the leaflet, and 61.3% were aware of potential side effects. Hydrocortisone 1% was the most recognized cream (45.1%), while 29.5% could not identify any corticosteroid cream. The leading indications were eczema (32.6%) and itchiness (17%). Adverse effects were reported by 39.9%, most commonly redness, increased hair growth, and skin thinning. Chi-square analyses showed that adverse effect reporting was associated with longer duration and higher frequency of use (p < 0.05), while regression analysis demonstrated that cream recognition was lower among males and higher among employed or retired individuals compared with housewives (p < 0.05).</p><p><strong>Conclusion: </strong>Topical corticosteroid use is widespread in Jordan, often obtained without prescription and with limited awareness of potency, indications, and risks. Targeted public education and stricter regulation of dispensing are needed to reduce misuse and ensure safer use.</p>","PeriodicalId":10447,"journal":{"name":"Clinical, Cosmetic and Investigational Dermatology","volume":"18 ","pages":"2285-2295"},"PeriodicalIF":2.2,"publicationDate":"2025-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12435496/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145074288","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Spanning 17 Years: Diagnostic Evolution from Lichen Planus Pigmentosus to Hyperpigmented Mycosis Fungoides. 跨越17年:从扁平苔藓到高色素蕈样真菌病的诊断进化。
IF 2.2 4区 医学
Clinical, Cosmetic and Investigational Dermatology Pub Date : 2025-09-11 eCollection Date: 2025-01-01 DOI: 10.2147/CCID.S541051
WeiFeng Zha, JunWei Lu
{"title":"Spanning 17 Years: Diagnostic Evolution from Lichen Planus Pigmentosus to Hyperpigmented Mycosis Fungoides.","authors":"WeiFeng Zha, JunWei Lu","doi":"10.2147/CCID.S541051","DOIUrl":"10.2147/CCID.S541051","url":null,"abstract":"<p><p>Lichen planus pigmentosus (LPP) and hyperpigmented mycosis fungoides (MF) represent two distinct rare cutaneous disorders. This case explores the potential association between LPP and hyperpigmented MF, a previously unreported progression. The authors report a 52-year-old male presenting with purplish-red macules on the abdomen and upper extremities subsequent to exposure to petrochemicals, initially diagnosed in 2007 with lichen planus (LP). In 2019, LPP was confirmed by histopathological evaluation of a skin biopsy obtained from an outside institution. Despite treatment with hydroxychloroquine sulfate tablets, the lesions exhibited disease progression. After 17 years, generalized hyperpigmentation gradually developed. Repeat biopsies and immunohistochemistry were performed in 2024, leading to the definitive diagnosis of hyperpigmented MF. The patient is currently managed with subcutaneous interferon alpha-2b (IFNα-2b) injections, with the rash color showing slight lightening. In conclusion, the cutaneous manifestations of MF demonstrate marked heterogeneity, requiring systematic clinical evaluation and histopathological assessment to facilitate accurate diagnosis and guide the development of stage-appropriate treatment protocols. Whether the transformation from LPP to hyperpigmented MF is rare, impossible, or a missed diagnosis remains to be further clarified with more reported cases.</p>","PeriodicalId":10447,"journal":{"name":"Clinical, Cosmetic and Investigational Dermatology","volume":"18 ","pages":"2297-2302"},"PeriodicalIF":2.2,"publicationDate":"2025-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12435356/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145074298","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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