Burgio G R, Martini A
Clinica Pediatrica, Università di Pavia, Policlinico S. Matteo, Italy.
Eur J Pediatr. 1990 Jan;149(4):224-31. doi: 10.1007/BF02106277.
Diffuse connective tissue diseases (DCTD) represent an heterogeneous group of disorders characterized by systemic inflammatory reactions that are currently classified on clinical grounds. Their aetiopathogenesis is largely unknown and appears to be very complex, associating exogenous factors with an immunogenetic predisposition. In the last decade, studies on human leukocyte antigen (HLA)-disease associations and antinuclear antibodies have provided some useful clues for the diagnosis and clinical management of DCTD.
弥漫性结缔组织病(DCTD)是一组异质性疾病,其特征为全身性炎症反应,目前根据临床依据进行分类。它们的发病机制在很大程度上尚不清楚,而且似乎非常复杂,将外源性因素与免疫遗传易感性联系在一起。在过去十年中,关于人类白细胞抗原(HLA)与疾病关联以及抗核抗体的研究为DCTD的诊断和临床管理提供了一些有用的线索。