混合性结缔组织病
医学
类风湿性关节炎
抗合成酶综合征
系统性红斑狼疮
皮肤病科
疾病
妇科
免疫学
病理
抗体
自身抗体
作者
Edwin Curraj,Mhedi Belkoniene,Carole Keutchakeu-Tchatcho,Maxime Ringwald,Camillo Ribi
标识
DOI:10.53738/revmed.2024.20.868.699
摘要
Mixed connective tissue disease (MCTD) is a rare autoimmune condition. Since its first description 50 years ago, its mere existence has been debated, given that it shares features of other autoimmune diseases, such as systemic lupus erythematosus (SLE), systemic sclerosis, inflammatory myopathy, rheumatoid arthritis and Sjogren's syndrome. Also, while antibodies to U1-RNP are essential for the diagnosis of MCTD, these antibodies may be expressed in other circumstances, such as in case of SLE. Nevertheless, the patient fulfilling criteria for MCTD needs specific management. In this review, we describe the clinical features and the potential complications of this complex disease, often wrongly disregarded as benign. We will also emphasize the recommended follow-up exams and address treatment, which is currently lacking formal recommendations.
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