Concomitant sarcoidosis, psoriasis, and eczema - immune patterns on the skin.

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Sebastian Sitaru, Alexander Zink, Tilo Biedermann, Susanne Annette Steimle-Grauer
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引用次数: 0

Abstract

Sarcoidosis is a rare and elusive chronic inflammatory disease. It can manifest itself in any organ, but preferentially affects the lungs and the skin. Our case of an elderly woman with cutaneous and pulmonary sarcoidosis presented with exacerbated itchy, scaly skin changes to our department. The clinical and histopathological findings were consistent with sarcoidosis and eczematized psoriasis. The case represents a unique presentation of sarcoidosis with cutaneous involvement and poses diagnostic and therapeutic challenges due to overlapping clinical features and histology covering the three diagnoses. We discuss the immunological complexities underlying this overlap and resulting possible treatment options, highlighting the role of dermatology in systemic autoimmune diseases involving the skin and the need for pathophysiology-based tailored management approaches in these diseases.

伴发肉样瘤病、银屑病和湿疹--皮肤上的免疫模式。
肉样瘤病是一种罕见而难以捉摸的慢性炎症性疾病。肉样瘤病可发生在任何器官,但好发于肺部和皮肤。我们的病例是一名患有皮肤和肺部肉样瘤病的老年妇女,她因皮肤瘙痒、鳞屑增多而到我科就诊。临床和组织病理学检查结果与肉样瘤病和湿疹化银屑病一致。该病例是肉样瘤病伴有皮肤受累的一种独特表现,由于三种诊断的临床特征和组织学均有重叠,给诊断和治疗带来了挑战。我们讨论了这种重叠背后的免疫学复杂性以及可能的治疗方案,强调了皮肤科在累及皮肤的全身性自身免疫性疾病中的作用,以及对这些疾病采取基于病理生理学的定制治疗方法的必要性。
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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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