Cutaneous presentations of systemic sclerosis in skin of colour: A systematic review

Alicia Podwojniak, Isabella J. Tan, Aliza Leiter, Hira Ghani, Bernard A. Cohen
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Abstract

Systemic sclerosis (SSc), a rheumatologic autoimmune disease, can present diversely, especially in patients with skin of colour (SOC). Differences in clinical manifestations among SOC individuals compared to predominantly White populations require a comprehensive examination to optimize diagnosis and treatment. This systematic review aims to explore the differences in SSc manifestations among individuals with SOC, identifying variations in disease severity, clinical features and psychosocial impacts. A systematic review of the literature was conducted following PRISMA guidelines. Databases searched included PubMed, SCOPUS, Cochrane and Web of Science, focusing on studies published within the last 10 years. Nine studies were selected and qualitatively analysed due to the heterogeneity of study types. Key findings highlight significant variations in disease severity and cutaneous clinical features among SOC cohorts compared to predominantly White populations. Raynaud's phenomenon was prevalent across all ethnicities; however, SOC groups exhibited fewer hallmark features of scleroderma, such as telangiectasias, calcinosis and digital swelling, which complicates diagnosis. SOC individuals showed a higher propensity for severe pulmonary complications and increased mortality rates. Atypical cutaneous presentations in SOC were associated with disease progression. Psychosocial impacts were more pronounced in SOC individuals, with greater awareness and dissatisfaction over cutaneous symptoms. Recognizing the atypical presentations of SSc in SOC is critical for early diagnosis and optimizing patient outcomes. The study underscores the need for further research to determine if observed differences are due to variations in prevalence, genetic factors or insufficient training in recognizing cutaneous manifestations in SOC. Enhanced awareness and targeted training for healthcare providers are essential to address these diagnostic challenges and improve care for SOC patients with SSc.

Abstract Image

系统性硬化症在有色皮肤中的皮肤表现:系统综述
系统性硬化症(SSc)是一种风湿性自身免疫性疾病,其表现形式多种多样,特别是在有色皮肤(SOC)患者中。与以白人为主的人群相比,SOC个体的临床表现差异需要全面检查以优化诊断和治疗。本系统综述旨在探讨SOC患者SSc表现的差异,识别疾病严重程度、临床特征和社会心理影响的差异。按照PRISMA指南对文献进行了系统的综述。搜索的数据库包括PubMed、SCOPUS、Cochrane和Web of Science,重点是过去10年发表的研究。由于研究类型的异质性,我们选择了9项研究并进行了定性分析。主要研究结果强调,与以白人为主的人群相比,SOC队列在疾病严重程度和皮肤临床特征方面存在显著差异。雷诺的现象在所有种族中都很普遍;然而,SOC组表现出较少的硬皮病标志性特征,如毛细血管扩张、钙质沉着和指部肿胀,这些特征使诊断复杂化。SOC个体表现出更高的严重肺部并发症倾向和更高的死亡率。SOC的非典型皮肤表现与疾病进展相关。社会心理影响在SOC个体中更为明显,对皮肤症状的认识和不满程度更高。认识到SOC中SSc的非典型表现对于早期诊断和优化患者预后至关重要。该研究强调了进一步研究的必要性,以确定观察到的差异是由于患病率的变化、遗传因素还是在识别SOC皮肤表现方面训练不足。提高对医疗保健提供者的认识和有针对性的培训对于解决这些诊断挑战和改善对伴有SSc的SOC患者的护理至关重要。
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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