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系统性自身免疫性风湿病作为副肿瘤现象:3 个说明性病例报告及文献综述。

Systemic autoimmune rheumatic diseases as paraneoplastic phenomena: 3 illustrative case reports and narrative review of the literature.

机构信息

Division of Rheumatology, University Hospitals Leuven, Leuven, Belgium.

Department of General Medical Oncology, University Hospitals Leuven, Leuven, Belgium.

出版信息

Acta Clin Belg. 2023 Oct;78(5):410-417. doi: 10.1080/17843286.2023.2183577. Epub 2023 Feb 27.

Abstract

OBJECTIVES

Systemic autoimmune rheumatic diseases can occur as paraneoplastic phenomena in the context of underlying malignancies. We present three illustrative clinical cases and a narrative literature review focusing on systemic sclerosis, dermatomyositis and palmar fasciitis and polyarthritis syndrome.

METHODS

Medical data of three patients from the University Hospitals Leuven were retrospectively and anonymously obtained and reviewed. A narrative review was performed, searching the databases of PubMed, Embase and Cochrane Library.

RESULTS

Systemic sclerosis, dermatomyositis and palmar fasciitis and polyarthritis syndrome are systemic autoimmune rheumatic diseases that can present as paraneoplastic phenomena. Systemic autoimmune rheumatic diseases are often associated with the presence of specific autoantibodies, some associated with a high likelihood of underlying malignancy. The presence of anti-ribonucleic acid polymerase III antibodies and anti-transcription intermediary factor 1 gamma antibodies indicates an increased risk of underlying cancer in systemic sclerosis and dermatomyositis, respectively. Individual patient prognosis can be improved through early detection of underlying malignancy, hence the importance of adequate cancer screening.

CONCLUSION

Some systemic autoimmune rheumatic diseases can appear as paraneoplastic phenomena, whereby the presence of specific autoantibodies is known to be related to the likelihood of underlying malignancy. We highlight the importance of clinician's knowledge of these distinct features, as it facilitates early detection and treatment of underlying malignancy, thereby improving individual patient prognosis.

摘要

目的

系统性自身免疫性风湿病可作为潜在恶性肿瘤的副肿瘤现象发生。我们展示了三个临床病例,并进行了系统性硬皮病、皮肌炎和掌筋膜-多发性关节炎综合征的叙述性文献综述。

方法

回顾性和匿名地从鲁汶大学医院获得了三名患者的医疗数据,并进行了审查。进行了叙述性文献复习,检索了 PubMed、Embase 和 Cochrane 图书馆的数据库。

结果

系统性硬皮病、皮肌炎和掌筋膜-多发性关节炎综合征是系统性自身免疫性风湿病,可表现为副肿瘤现象。系统性自身免疫性风湿病常与特定自身抗体的存在相关,其中一些与潜在恶性肿瘤的高可能性相关。抗核糖核酸聚合酶 III 抗体和抗转录中介因子 1γ 抗体的存在分别表明系统性硬皮病和皮肌炎患者存在潜在癌症的风险增加。通过早期检测潜在的恶性肿瘤,可以改善个体患者的预后,因此充分的癌症筛查非常重要。

结论

一些系统性自身免疫性风湿病可表现为副肿瘤现象,已知特定自身抗体的存在与潜在恶性肿瘤的可能性相关。我们强调了临床医生了解这些不同特征的重要性,因为这有助于早期发现和治疗潜在的恶性肿瘤,从而改善个体患者的预后。

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