期刊文献+

临床无肌病性皮肌炎的诊断及治疗 被引量:3

The diagnosis and treatment of clinically amyopathic dermatomyositis
暂未订购
导出
摘要 临床无肌病性皮肌炎被认为是皮肌炎的一种少见类型,是指具有皮肌炎的典型皮损,临床上不表现为肌无力,肌酶谱正常或仅轻度异常,分为无肌病性皮肌炎和低肌病性皮肌炎。部分患者与严重的肺部病变及恶性肿瘤相关,而部分严重患者对糖皮质激素治疗不敏感,故早期发现和正确认识该病并给予合理的干预,对改善患者预后非常重要。 Clinically amyopathic dermatomyositis(C-ADM) is a rare form of dermatomyositis (DM), in which typical skin changes contrast with minimal or absent muscle abnormalities, including amyopathic dermatomyositis (ADM) and hypomyopathic dermatomyositis (HDM). In some cases, it is associated with severe lung lesions and malignant tumors. Patients with severe disease of this kind are unresponsive to glucocorticoids. So early detection and correct understanding of the disease, and a proper intervention to it is very important for improving patient outcomes. In this paper, the diagnosis and treatment of clinically amyopathic dermatomyositisare are summarized as follows.
出处 《实用皮肤病学杂志》 2012年第5期275-277,共3页 Journal of Practical Dermatology
关键词 皮肌炎 临床无肌病性 肺病 间质性 诊断 治疗 Dermatomyositis Clinically amyopathic Lung disease, interstitial Diagnosis Treatment
  • 相关文献

参考文献23

  • 1Krain L. Dermatomyositis in six patients without initial muscle involvement[J].Archives of Dermatology,1975,(02):241-245.
  • 2Pearson CM. Polymyositis and Dermatomyositis[A].Philadelphia:Lea & Febiger,1979.742.
  • 3Euwer RL,Sontheimer RD. Amyopathic dermatomyositis.Presentation of six cases and review of the literature[J].Journal of the American Academy of Dermatology,1991,(6 Pt 1):959-966.
  • 4Sontheimer RD. Cutaneous features of classic dermatomyositis and amyopathic dermatomyositis[J].Current Opinion in Rheumatology,1999,(06):475-482.doi:10.1097/00002281-199911000-00006.
  • 5Stonecipher MR,Jorizzo JL,Monu J. Dermatomyositis with normal muscle enzyme concentrations.A single-blind study of the diagnostic value of magnetic resonance imaging and ultrasound[J].Archives of Dermatology,1994,(10):1294-1299.
  • 6Park JH,Olsen NJ,King L1. Use of magnetic resonance imaging and P-31 magnetic resonance spectroscopy to detect and quantity muscle dysfunction in the amyopathic and myopathic variants of dermatomyositis[J].Arthritis and Rheumatism,1995,(01):68-77.doi:10.1002/art.1780380111.
  • 7Sato S,Hirakata M,Kuwana M. Autoantibodies to a 140-kd polypeptide,CADM-140m,in Japanese patients with clinically amyopathic dermatomyositis[J].Arthritis and Rheumatism,2005,(05):1571-1576.doi:10.1002/art.21023.
  • 8Sato S. Autoantibodies specifically detected in patients with polymyositis/dermatomyositis[J].Nihon Rinsho Meneki Gakkai Kai-shi,2006,(02):85-93.
  • 9Yamasaki Y,Yamada H,Nozaki T. Unusually high frequency of autoantibodies to PL-7 associated with milder muscle disease in Japanese patients with polymyositis/dermatomyositis[J].Arthritis and Rheumatism,2006,(06):2004-2009.
  • 10Nakashima R,Imura Y,Kobayashi S. The RIG-I-like receptor IFIH1/MDA5 is a dermatomyositis-specific autoantigen identified by the anti-CADM-140 antibody[J].Rheumatology(Oxford),2010,(03):433-440.

同被引文献17

引证文献3

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部