混合性结缔组织病30例临床分析

中国医师进修杂志 Pub Date : 2000-03-15 DOI:10.3760/CMA.J.ISSN.1673-4904.2000.03.012

Xuebing Feng

{"title":"混合性结缔组织病30例临床分析","authors":"Xuebing Feng","doi":"10.3760/CMA.J.ISSN.1673-4904.2000.03.012","DOIUrl":null,"url":null,"abstract":"Objective:To evaluate the clinical features and correlation with disease course of mixed connective tissue disease (MCTD).Methods:30 patients with definite MCTD were analyzed retropectively by their clinical manifestation and immunological features,treatments and prognosis.They were assigned to two groups according to their courses of the disease (group A5 years and group B ≥5 years).Results:The primarily incipient symptoms of MCTD were Raynaud's phenomenon and arthralgia/arthritis.Morbidity of Raynaud's phenomenon in group A was statistically significantly higher than in group B(P0.01) while incidence of pulmonary hypertension or interstitial fibrosis was higher in group B (P0.05).Laboratroy indices showed that abnormal IgG and ESR were easy to be seen and renal dysfunction with high uria protein was found in 26.7% patients.Mortality was zero in group A while 25% in group B.Conclusion:MCTD is not a benign disease.With disease duration prolonged,incidence of vital organ dysfunction increases and mortality tends to elevate.","PeriodicalId":10229,"journal":{"name":"中国医师进修杂志","volume":"27 1","pages":"26-28"},"PeriodicalIF":0.0000,"publicationDate":"2000-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"THE CLINICAL ANALYSIS OF MIXED CONNECFIVE TISSUE DISEASE:A REPORT OF 30 CASES\",\"authors\":\"Xuebing Feng\",\"doi\":\"10.3760/CMA.J.ISSN.1673-4904.2000.03.012\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Objective:To evaluate the clinical features and correlation with disease course of mixed connective tissue disease (MCTD).Methods:30 patients with definite MCTD were analyzed retropectively by their clinical manifestation and immunological features,treatments and prognosis.They were assigned to two groups according to their courses of the disease (group A5 years and group B ≥5 years).Results:The primarily incipient symptoms of MCTD were Raynaud's phenomenon and arthralgia/arthritis.Morbidity of Raynaud's phenomenon in group A was statistically significantly higher than in group B(P0.01) while incidence of pulmonary hypertension or interstitial fibrosis was higher in group B (P0.05).Laboratroy indices showed that abnormal IgG and ESR were easy to be seen and renal dysfunction with high uria protein was found in 26.7% patients.Mortality was zero in group A while 25% in group B.Conclusion:MCTD is not a benign disease.With disease duration prolonged,incidence of vital organ dysfunction increases and mortality tends to elevate.\",\"PeriodicalId\":10229,\"journal\":{\"name\":\"中国医师进修杂志\",\"volume\":\"27 1\",\"pages\":\"26-28\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2000-03-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"中国医师进修杂志\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.3760/CMA.J.ISSN.1673-4904.2000.03.012\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"中国医师进修杂志","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3760/CMA.J.ISSN.1673-4904.2000.03.012","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}

引用次数: 0

摘要

目的:探讨混合性结缔组织病(MCTD)的临床特点及其与病程的关系。方法:回顾性分析30例确诊MCTD患者的临床表现、免疫学特征、治疗及预后。根据病程分为两组(a组5年，B组≥5年)。结果:MCTD的早期症状主要为雷诺氏现象和关节痛/关节炎。A组雷诺现象发生率高于B组(P0.01)， B组肺动脉高压、间质纤维化发生率高于B组(P0.05)。实验室指标显示，IgG和ESR易出现异常，26.7%的患者出现肾功能不全伴高尿蛋白。A组死亡率为零，b组死亡率为25%。结论:MCTD不是良性疾病。随着病程的延长，重要器官功能障碍的发生率增加，死亡率有升高的趋势。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

查看原文本刊更多论文

THE CLINICAL ANALYSIS OF MIXED CONNECFIVE TISSUE DISEASE:A REPORT OF 30 CASES

Objective:To evaluate the clinical features and correlation with disease course of mixed connective tissue disease (MCTD).Methods:30 patients with definite MCTD were analyzed retropectively by their clinical manifestation and immunological features,treatments and prognosis.They were assigned to two groups according to their courses of the disease (group A5 years and group B ≥5 years).Results:The primarily incipient symptoms of MCTD were Raynaud's phenomenon and arthralgia/arthritis.Morbidity of Raynaud's phenomenon in group A was statistically significantly higher than in group B(P0.01) while incidence of pulmonary hypertension or interstitial fibrosis was higher in group B (P0.05).Laboratroy indices showed that abnormal IgG and ESR were easy to be seen and renal dysfunction with high uria protein was found in 26.7% patients.Mortality was zero in group A while 25% in group B.Conclusion:MCTD is not a benign disease.With disease duration prolonged,incidence of vital organ dysfunction increases and mortality tends to elevate.

求助全文

通过发布文献求助，成功后即可免费获取论文全文。去求助

来源期刊

中国医师进修杂志

自引率

0.00%

发文量

26239

期刊介绍： Chinese Journal of Postgraduates of Medicine (founded in 1978, monthly) is one of the series of journals of the Chinese Medical Association (CMA) under the supervision of the National Health Commission of the People's Republic of China, sponsored by the Chinese Medical Association (CMA) and Dalian Institute of Theoretical Medicine (DITM). It is a core journal of Chinese science and technology, a statistical source journal of Chinese scientific and technical papers, and a statistical source journal of China Academic Journal Impact Factor Annual Report. The journal adheres to the purpose of using continuing medical education and post training, highlights new theories, new knowledge, new methods and new technologies, and focuses on the combination of theory and practice, and the combination of popularisation and improvement. Main columns: Special tutorials, expert forums, clinical treatises, clinical experience, reviews and lectures, continuing medical education, teaching and research, advanced training forum, drugs and clinics, overview of progress, introduction of new technologies, imaging and clinics, lessons learnt, discussions and evaluations, case reports, discussions of clinical cases, conference proceedings, and domestic and international academic developments. The main target readers are clinical medical personnel in internal medicine, surgery, gynaecology, paediatrics and ophthalmology.