George G Mitroi, Mihaela Roxana Mitroi, George F Mitroi, Laura Simona Ianoși
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Severity scores such as SCORing Atopic Dermatitis (SCORAD) and dermatological life quality index (DLQI) play pivotal roles in evaluating disease severity and its impact on quality of life, guiding the development of personalized treatment strategies for adult AD patients. In this study, we aim to present four compelling cases of adult-onset atopic dermatitis, each offering unique insights into this increasingly recognized phenomenon. What makes these cases particularly noteworthy is the absence of any prior atopic history in two out of four patients, challenging the conventional understanding of AD as a condition predominantly linked to childhood. Moreover, the clinical presentation in all four cases was markedly atypical, underscoring the elusive nature of adult-onset AD diagnosis. In our investigation, interleukin 4 (IL-4), interleukin 13 (IL-13), and Immunoglobulin E (IgE) were utilized as diagnostic biomarkers for our patient cohort. Given the established pivotal roles of IL-4 and IL-13 in AD pathogenesis, elevated serum levels of these biomarkers, although not universally endorsed, hold potential for diagnostic utility. 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In this study, we aim to present four compelling cases of adult-onset atopic dermatitis, each offering unique insights into this increasingly recognized phenomenon. What makes these cases particularly noteworthy is the absence of any prior atopic history in two out of four patients, challenging the conventional understanding of AD as a condition predominantly linked to childhood. Moreover, the clinical presentation in all four cases was markedly atypical, underscoring the elusive nature of adult-onset AD diagnosis. In our investigation, interleukin 4 (IL-4), interleukin 13 (IL-13), and Immunoglobulin E (IgE) were utilized as diagnostic biomarkers for our patient cohort. Given the established pivotal roles of IL-4 and IL-13 in AD pathogenesis, elevated serum levels of these biomarkers, although not universally endorsed, hold potential for diagnostic utility. 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引用次数: 0
摘要
特应性皮炎(AD)是儿童中最常见的慢性炎症性皮肤病之一,其特点是皮肤屏障功能障碍和免疫系统异常。特应性皮炎历来被视为儿童疾病,但最近的研究结果表明,特应性皮炎在成人中的发病率很高,这促使人们对这一人群进行深入研究。由于缺乏公认的生物标志物,诊断主要取决于主观临床评估。因此,人们正在努力确定可靠的生物标志物,以提高诊断的准确性。本文强调,尽管注意力缺失症在儿科很常见,但在成人中却很少被诊断出来,因此有必要在成人群体中提高意识并采取有针对性的诊断方法。SCORing特应性皮炎(SCORAD)和皮肤病生活质量指数(DLQI)等严重程度评分在评估疾病严重程度及其对生活质量的影响方面起着关键作用,可指导成人 AD 患者制定个性化治疗策略。在本研究中,我们旨在介绍四个令人信服的成人特应性皮炎病例,每个病例都为这一日益被认可的现象提供了独特的见解。这些病例尤其值得注意的是,四例患者中有两例之前没有任何特应性病史,这对传统上认为 AD 主要与儿童期有关的认识提出了挑战。此外,所有四例患者的临床表现都明显不典型,这凸显了成人发病型 AD 诊断的难以捉摸性。在我们的研究中,白细胞介素4(IL-4)、白细胞介素13(IL-13)和免疫球蛋白E(IgE)被用作患者群的诊断生物标志物。鉴于IL-4和IL-13在AD发病机制中的关键作用已经确立,这些生物标记物的血清水平升高虽然没有得到普遍认可,但具有潜在的诊断作用。此外,IgE水平的升高表明了过敏反应和炎症的固有特性,强调了其作为AD管理的关键生物标志物和治疗目标的重要性。
Case Series Analysis of Late-Onset Atopic Dermatitis: Unraveling Clinical Variants.
Atopic Dermatitis (AD), recognized as one of the most prevalent chronic inflammatory skin disorders among children, is characterized by skin barrier dysfunction and immune system abnormalities. Historically viewed as a childhood condition, recent findings underscore a notable prevalence of AD in adults, prompting a critical examination of this demographic. Diagnosis hinges largely on subjective clinical assessments due to the absence of universally accepted biomarkers. Consequently, efforts are underway to identify dependable biomarkers to enhance diagnostic precision. This paper underscores the scarcity of AD diagnoses in adults despite its pediatric prominence, emphasizing the need for heightened awareness and tailored diagnostic approaches in adult populations. Severity scores such as SCORing Atopic Dermatitis (SCORAD) and dermatological life quality index (DLQI) play pivotal roles in evaluating disease severity and its impact on quality of life, guiding the development of personalized treatment strategies for adult AD patients. In this study, we aim to present four compelling cases of adult-onset atopic dermatitis, each offering unique insights into this increasingly recognized phenomenon. What makes these cases particularly noteworthy is the absence of any prior atopic history in two out of four patients, challenging the conventional understanding of AD as a condition predominantly linked to childhood. Moreover, the clinical presentation in all four cases was markedly atypical, underscoring the elusive nature of adult-onset AD diagnosis. In our investigation, interleukin 4 (IL-4), interleukin 13 (IL-13), and Immunoglobulin E (IgE) were utilized as diagnostic biomarkers for our patient cohort. Given the established pivotal roles of IL-4 and IL-13 in AD pathogenesis, elevated serum levels of these biomarkers, although not universally endorsed, hold potential for diagnostic utility. Furthermore, heightened levels of IgE, indicative of allergic responses and inflammation inherent to the condition, emphasize its significance as a key biomarker and therapeutic target in AD management.