mctd

Methods 26 patients with MCTD were evaluated by clinical , roentgenologic and lung functional observation .

方法选择26例混合性结缔组织病患者，进行临床、放射学及肺功能的观察。

After years of observation of a high number of cases , the same symptoms , it is generally considered an independent MCTD diseases .

经多年观察大量病例，症状不变，故人们普遍认为MCTD是一种独立的疾病。

Conclusion : The detection of serum anti-72000 protein from egg nucleus antibodies is useful for diagnosis and follow-up of MCTD cases .

结论：MCTD患者血清抗鸡卵核中72000蛋白抗体检测，对MCTD诊断有较高的价值，在治疗随访中也可起到一定的临床提示作用。

Objective : To analyse the specific antigens extracted from egg nucleus as diagnostic antigens in patients with mixed connective tissue disease ( MCTD ) .

目的：分析鸡卵核提取物中检测混合性结缔组织病（MCTD）的特异性抗原成份。

Objective : To study the correlation between anti-72000 protein from egg nucleus antibodies and the activity parameters of mixed connective tissue disease ( MCTD ) .

目的：通过检测混合性结缔组织病（MCTD）患者血清抗鸡卵核中72000蛋白抗体，研究其与MCTD有关指标的关系，以探讨该抗体在MCTD发病中的作用。

TCM theoretical research : For mixed connective tissue disease MCTD and overlap syndrome , and so on , there is no book in the Chinese clearly documented and discussed in detail .

中医理论研究：对于混合结缔组织病MCTD和重叠综合征等，在中医典籍中并无明确记载和详细论述。

Clinical and Autopsy findings of 1 case with Mixed Connective Tissue Disease ( MCTD ) associated with severe pulmonary hypertension , died of right heart failure and pulmonary infection , was reported .

1例混合结缔组织病伴肺动脉高压患者，死于右心衰竭及肺部感染。

There was no cross reaction in the sera from 72 patients with dermatomyositis or polymyositis ( DM / PM ), from 48 patients with progressed systemic scleroderma ( PSS ), and from 78 patients with mixed connective tissue disease ( MCTD ) .

对皮肌炎和多发性肌炎（DM/PM）72份、硬皮病（PSS）48份和混合性结缔组织病（MCTD）78份血清亦无交叉反应出现。

Method : A retrospective analysis was carried out in 30 patients with pulmonary hypertension ( PHT ) secondary to rheumatic diseases including 17 with systemic lupus erythematosus ( SLE ) , 8 with mixed connective tissue disease ( MCTD ) and 5 with systemic sclerosis ( SSc ) .

方法：对30例本病住院患者的临床资料作回顾性研究。其中继发于系统性红斑狼疮17例，混合性结缔组织病8例，系统性硬化症5例。

Results : The primarily incipient symptoms of MCTD were Raynaud 's phenomenon , the next symptoms were febrile 、 arthralgia / arthritis and myositis . Myositis and sclerodactyly / finger swollen were easy to be seen in patients with pulmonary artery hypertension / pulmonary interstitial fibrosis .

结果：MCTD最常见的临床表现为雷诺现象，其次为发热、关节肿/痛和肌炎，有肺间质病变朋市动脉高压的患者肌炎和硬指/手指肿胀的出现率高；