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复发性多软骨炎:最新研究进展并附三例病例报告。

Relapsing polychondritis: state-of-the-art review with three case presentations.

机构信息

Department of Rheumatology, Rehabilitation and Internal Medicine, Poznan University of Medical Sciences, Poznan, Poland.

出版信息

Postgrad Med. 2021 Nov;133(8):953-963. doi: 10.1080/00325481.2021.1979873. Epub 2021 Sep 30.

Abstract

BACKGROUND

Relapsing polychondritis (RPC) is a complex immune-mediated systemic disease affecting cartilaginous tissue and proteoglycan-rich organs. The most common and earliest clinical features are intermittent inflammation involving the auricular and nasal regions, although all cartilage types can be potentially affected. The life-threatening effects of rpc involve the tracheobronchial tree and cardiac connective components. Rpc is difficult to identify among other autoimmune comorbidities; diagnosis is usually delayed and based on nonspecific clinical symptoms with limited laboratory aid and investigations. Medications can vary, from steroids, immunosuppressants, and biologics, including anti-tnf alpha antagonist drugs.

METHOD

Information on updated etiology, clinical symptoms, diagnosis, and treatment of rpc has been obtained via extensive research of electronic literature published between 1976 and 2019 using PubMed and medline databases. English was the language of use. Search inputs included 'relapsing polychondritis,' 'polychondritis,' 'relapsing polychondritis symptoms,' and 'treatment of relapsing polychondritis.' Published articles in English that outlined and reported rpc's clinical manifestations and treatment ultimately met the inclusion criteria. Articles that failed to report the above and reported on other cartilaginous diseases met the exclusion criteria.

RESULT

Utilizing an extensive overview of work undertaken in critical areas of RPC research, this review intends to further explore and educate the approach to this disease in all dimensions from pathophysiology, diagnosis, and management.

CONCLUSION

RPC is a rare multi-systemic autoimmune disease and possibly fatal. The management remains empiric and is identified based on the severity of the disease per case. The optimal way to advance is to continue sharing data on RPC from reference centers; furthermore, clinical trials in randomized control groups must provide evidence-based treatment and management. Acquiring such information will refine the current knowledge of RPC, which will improve not only treatment but also diagnostic methods, including imaging and biological markers.

摘要

背景

复发性多软骨炎(RPC)是一种复杂的免疫介导的全身性疾病,影响软骨组织和富含蛋白聚糖的器官。最常见和最早的临床特征是涉及耳廓和鼻区的间歇性炎症,尽管所有类型的软骨都可能受到影响。危及生命的 rpc 影响涉及气管支气管树和心脏结缔组织成分。rpc 在其他自身免疫性合并症中难以识别;诊断通常延迟,基于非特异性临床症状,实验室辅助和检查有限。药物治疗各不相同,包括类固醇、免疫抑制剂和生物制剂,包括抗 TNFα 拮抗剂药物。

方法

通过广泛研究 1976 年至 2019 年期间在 PubMed 和 Medline 数据库上发表的电子文献,获得了关于 rpc 更新的病因、临床症状、诊断和治疗的信息。使用的语言是英语。搜索输入包括“复发性多软骨炎”、“多软骨炎”、“复发性多软骨炎症状”和“复发性多软骨炎的治疗”。最终符合纳入标准的是用英语概述和报告 rpc 临床表现和治疗的已发表文章。不符合纳入标准的文章报告了其他软骨疾病。

结果

利用对 RPC 研究关键领域所做工作的广泛概述,本综述旨在从病理生理学、诊断和管理等各个方面进一步探讨和教育这种疾病的处理方法。

结论

RPC 是一种罕见的多系统自身免疫性疾病,可能致命。管理仍然是经验性的,根据每个病例的疾病严重程度确定。进一步的方法是继续从参考中心共享有关 RPC 的数据;此外,必须在随机对照试验中提供循证治疗和管理。获得此类信息将完善目前对 RPC 的认识,这不仅将改善治疗方法,还将改善包括成像和生物标志物在内的诊断方法。

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