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本文引用的文献

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[Originators and eponyms of dermatomyositis : Ernst Leberecht Wagner (1821-1888) and Heinrich Unverricht (1853-1912)].
Z Rheumatol. 2016 May;75(4):429-34. doi: 10.1007/s00393-015-0008-8.
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Development of an internationally agreed minimal dataset for juvenile dermatomyositis (JDM) for clinical and research use.制定一个国际认可的用于临床和研究的青少年皮肌炎(JDM)最小数据集。
Trials. 2015 Jun 12;16:268. doi: 10.1186/s13063-015-0784-0.
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Disease patterns of juvenile dermatomyositis from Western India.印度西部青少年皮肌炎的疾病模式。
Indian Pediatr. 2013 Oct;50(10):961-3. doi: 10.1007/s13312-013-0260-4. Epub 2013 Apr 5.
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Cardiac involvement in adult polymyositis or dermatomyositis: a systematic review.成人多发性肌炎或皮肌炎的心脏受累:系统评价。
Clin Cardiol. 2012 Nov;35(11):686-91. doi: 10.1002/clc.22026. Epub 2012 Jul 30.
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Deciphering the clinical presentations, pathogenesis, and treatment of the idiopathic inflammatory myopathies.解读特发性炎性肌病的临床表现、发病机制和治疗方法。
JAMA. 2011 Jan 12;305(2):183-90. doi: 10.1001/jama.2010.1977.
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Juvenile dermatomyositis: new developments in pathogenesis, assessment and treatment.幼年特发性关节炎:发病机制、评估和治疗的新进展。
Best Pract Res Clin Rheumatol. 2009 Oct;23(5):665-78. doi: 10.1016/j.berh.2009.07.007.
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Complete and sustained remission of juvenile dermatomyositis resulting from aggressive treatment.积极治疗使青少年皮肌炎实现完全且持续缓解。
Arthritis Rheum. 2009 Jun;60(6):1825-1830. doi: 10.1002/art.24571.
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Twelve years experience of juvenile dermatomyositis in North India.印度北部青少年皮肌炎的十二年经验。
Rheumatol Int. 2006 Apr;26(6):510-5. doi: 10.1007/s00296-005-0030-2. Epub 2005 Sep 15.
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History of infection before the onset of juvenile dermatomyositis: results from the National Institute of Arthritis and Musculoskeletal and Skin Diseases Research Registry.青少年皮肌炎发病前的感染史:来自美国国立关节炎、肌肉骨骼和皮肤病研究所研究注册库的结果
Arthritis Rheum. 2005 Apr 15;53(2):166-72. doi: 10.1002/art.21068.
10
Long-term survival of patients with idiopathic inflammatory myopathies according to clinical features: a longitudinal study of 162 cases.根据临床特征分析特发性炎性肌病患者的长期生存率:一项对162例患者的纵向研究
Medicine (Baltimore). 2004 Jan;83(1):35-42. doi: 10.1097/01.md.0000109755.65914.5e.

亚临床心脏受累的青少年皮肌炎急性表现:1例罕见病例

Acute Presentation of Juvenile Dermatomyositis with Subclinical Cardiac Involvement: A Rare Case.

作者信息

Khera Rhythm, Khare Shrayash, Singh Shailendra Kumar

机构信息

Junior Resident, Department of Pediatrics, Sarojini Naidu Medical College , Agra, Uttar Pradesh, India .

Intern, Sarojini Naidu Medical College , Agra, Uttar Pradesh, India .

出版信息

J Clin Diagn Res. 2016 Dec;10(12):SD01-SD03. doi: 10.7860/JCDR/2016/20925.9008. Epub 2016 Dec 1.

DOI:10.7860/JCDR/2016/20925.9008
PMID:28208969
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5296542/
Abstract

Cardiac involvements are common in patients with Dermatomyositis, most of which are not severe enough to present definite or readily observable symptoms. However, Cardiovascular (CVS) manifestations constitute a major cause of death in these patients. The most frequently reported clinically evident of CVS manifestations in-patient of dermatomyositis are Congestive Heart Failure (CHF), conduction aberrations, that may predispose to complete heart block and coronary artery disease. The principal pathophysiological mechanisms that may produce these cardiac manifestations involve coronary artery disease as well as small vessels vasculitis of the myocardium. Our case of a seven-year-old boy represent a unique manifestation of prolong PR interval with no overt clinical manifestation and who responded well to immunosuppressive treatment. His clinical, laboratory and investigative features of Juvenile Dermatomyositis (JDM) is presented here. It is hoped that this case will heighten the index of suspicion of cardiac condition in patients with JDM among medical practitioners.

摘要

心脏受累在皮肌炎患者中很常见,其中大多数病情并不严重,不足以出现明确或易于观察到的症状。然而,心血管(CVS)表现是这些患者的主要死因。皮肌炎患者临床上最常报告的明显CVS表现是充血性心力衰竭(CHF)、传导异常,这可能易导致完全性心脏传导阻滞和冠状动脉疾病。可能产生这些心脏表现的主要病理生理机制包括冠状动脉疾病以及心肌小血管血管炎。我们这个七岁男孩的病例代表了一种独特的表现,即PR间期延长且无明显临床表现,并且对免疫抑制治疗反应良好。本文介绍了他青少年皮肌炎(JDM)的临床、实验室和检查特征。希望这个病例能提高医生对JDM患者心脏状况的怀疑指数。