Udoff E J, Genant H K, Kozin F, Ginsberg M
Radiology. 1977 Sep;124(3):613-8. doi: 10.1148/124.3.613.
Mixed connective tissue disease (MCTD) is a serologically distinct entity defined by a ribonuclease-sensitive extractable nuclear antigen. This unusual overlap syndrome has clinical features of scleroderma, systemic lupus erythematosus, polymyositis, and rheumatoid arthritis. In order to define the radiographic changes in MCTD, radiographs of the hands of 17 patients were studied, utilizing a fine-detail technique. Diffuse and periarticular osteopenia were found in 8 and 10 patients, respectively; soft-tissue swelling in 11; erosive changes in 9; joint-space narrowing in 7; tuft resorption and soft-tissue atrophy in 6; and subluxations in 2. In individual cases radiographs may appear normal or exhibit features of scleroderma, systemic lupus erythematosus or rheumatoid arthritis, thereby mirroring the clinical diversity of this entity.
混合性结缔组织病(MCTD)是一种血清学上独特的疾病实体,由核糖核酸酶敏感的可提取核抗原所定义。这种不寻常的重叠综合征具有硬皮病、系统性红斑狼疮、多发性肌炎和类风湿关节炎的临床特征。为了明确MCTD的影像学改变,采用精细技术对17例患者的手部X线片进行了研究。分别有8例和10例患者出现弥漫性和关节周围骨质减少;11例出现软组织肿胀;9例出现侵蚀性改变;7例出现关节间隙变窄;6例出现指骨吸收和软组织萎缩;2例出现半脱位。在个别病例中,X线片可能表现正常,或呈现硬皮病、系统性红斑狼疮或类风湿关节炎的特征,从而反映出该疾病实体的临床多样性。