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Incidence of dermatomyositis and clinically amyopathic dermatomyositis: a population-based study in Olmsted County, Minnesota.皮肌炎及临床无肌病性皮肌炎的发病率:明尼苏达州奥姆斯特德县的一项基于人群的研究
Arch Dermatol. 2010 Jan;146(1):26-30. doi: 10.1001/archdermatol.2009.328.
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Amyopathic dermatomyositis: retrospective review of 37 cases.无肌病性皮肌炎:37例回顾性研究
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Favorable Response to Adjuvant Tofacitinib in a Case of Anti-Melanoma Differentiation-Associated Gene-5 Antibody Positive Clinically Amyopathic Dermatomyositis.托法替布辅助治疗抗黑色素瘤分化相关基因5抗体阳性的临床无肌病性皮肌炎1例疗效良好
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本文引用的文献

1
Number, characteristics, and classification of patients with dermatomyositis seen by dermatology and rheumatology departments at a large tertiary medical center.一家大型三级医疗中心皮肤科和风湿科诊治的皮肌炎患者的数量、特征及分类
J Am Acad Dermatol. 2007 Dec;57(6):937-43. doi: 10.1016/j.jaad.2007.08.024. Epub 2007 Oct 17.
2
A systematic review of adult-onset clinically amyopathic dermatomyositis (dermatomyositis siné myositis): a missing link within the spectrum of the idiopathic inflammatory myopathies.成人起病的临床无肌病性皮肌炎(无肌性皮肌炎)的系统评价:特发性炎性肌病谱系中的缺失环节
J Am Acad Dermatol. 2006 Apr;54(4):597-613. doi: 10.1016/j.jaad.2005.10.041. Epub 2006 Jan 23.
3
Polymyositis and dermatomyositis associated with malignancy: a 30-year retrospective study.与恶性肿瘤相关的多发性肌炎和皮肌炎:一项30年回顾性研究。
Int J Dermatol. 2002 Nov;41(11):729-34. doi: 10.1046/j.1365-4362.2002.01648.x.
4
Dermatomyositis: an overview of recent progress with emphasis on dermatologic aspects.皮肌炎:近期进展概述,重点关注皮肤方面
Dermatol Clin. 2002 Jul;20(3):387-408. doi: 10.1016/s0733-8635(02)00021-9.
5
Would a new name hasten the acceptance of amyopathic dermatomyositis (dermatomyositis siné myositis) as a distinctive subset within the idiopathic inflammatory dermatomyopathies spectrum of clinical illness?一个新名称会加速无肌病性皮肌炎(无肌性皮肌炎)被接受为特发性炎症性皮肌病临床疾病谱中的一个独特亚组吗?
J Am Acad Dermatol. 2002 Apr;46(4):626-36. doi: 10.1067/mjd.2002.120621.
6
Amyopathic dermatomyositis: retrospective review of 37 cases.无肌病性皮肌炎:37例回顾性研究
J Am Acad Dermatol. 2002 Apr;46(4):560-5. doi: 10.1067/mjd.2002.120620.
7
[A case of amyopathic dermatomyositis with rapidly progressive interstitial pneumonia].[一例伴快速进展性间质性肺炎的无肌病性皮肌炎病例]
Ryumachi. 2000 Aug;40(4):705-10.
8
Cutaneous features of classic dermatomyositis and amyopathic dermatomyositis.典型皮肌炎和无肌病性皮肌炎的皮肤特征。
Curr Opin Rheumatol. 1999 Nov;11(6):475-82.
9
[A case of amyopathic dermatomyositis associated with interstitial pneumonitis].[1例伴间质性肺炎的无肌病性皮肌炎]
Ryumachi. 1997 Oct;37(5):714-8.
10
Amyopathic dermatomyositis associated with malignancy.与恶性肿瘤相关的无肌病性皮肌炎。
Int J Dermatol. 1996 Sep;35(9):663-4. doi: 10.1111/j.1365-4362.1996.tb03698.x.

皮肌炎及临床无肌病性皮肌炎的发病率:明尼苏达州奥姆斯特德县的一项基于人群的研究

Incidence of dermatomyositis and clinically amyopathic dermatomyositis: a population-based study in Olmsted County, Minnesota.

作者信息

Bendewald Margo J, Wetter David A, Li Xujian, Davis Mark D P

机构信息

Mayo Medical School, College of Medicine, Mayo Clinic, 200 First St SW, Rochester, MN 55905, USA.

出版信息

Arch Dermatol. 2010 Jan;146(1):26-30. doi: 10.1001/archdermatol.2009.328.

DOI:10.1001/archdermatol.2009.328
PMID:20083689
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2886726/
Abstract

OBJECTIVES

To identify new and existing cases of dermatomyositis and its subtypes in Olmsted County, Minnesota, from 1976 through 2007, and to establish a population-based estimate of the incidence and prevalence of dermatomyositis and amyopathic dermatomyositis.

DESIGN

Retrospective population-based study.

SETTING

Community-based epidemiology project. Patients Patients with a diagnosis of dermatomyositis were identified from the Rochester Epidemiology Project.

MAIN OUTCOME MEASURES

Incidence of dermatomyositis and clinically amyopathic dermatomyositis and risk of malignancy in clinically amyopathic dermatomyositis.

RESULTS

Of the 29 patients identified, 6 (21%) had the clinically amyopathic subtype of dermatomyositis and 22 (76%) were female. Overall age- and sex-adjusted incidence of dermatomyositis including all subtypes was 9.63 (95% confidence interval [CI], 6.09-13.17) per 1 million persons and 2.08 (95% CI, 0.39-3.77) per 1 million persons for clinically amyopathic dermatomyositis. Age- and sex-adjusted prevalence for all subtypes of dermatomyositis was 21.42 (95% CI, 13.07-29.77) per 100,000 persons. Eight patients (28%) had a malignant condition during the study period; the risk of malignancy (odds ratio) for classic dermatomyositis compared with clinically amyopathic dermatomyositis was 4.61 but was not statistically significant (95% CI, 0.22-96.09) (P=.44).

CONCLUSIONS

Dermatomyositis is a rare disease, and clinically amyopathic dermatomyositis represents an estimated 20% of all dermatomyositis cases. Larger population-based studies are needed to estimate the risk of malignancy associated with subtypes of dermatomyositis, particularly clinically amyopathic dermatomyositis.

摘要

目的

确定1976年至2007年明尼苏达州奥尔姆斯特德县皮肌炎及其亚型的新发病例和现患病例,并基于人群对皮肌炎和无肌病性皮肌炎的发病率和患病率进行估计。

设计

基于人群的回顾性研究。

设置

社区流行病学项目。患者 从罗切斯特流行病学项目中识别出诊断为皮肌炎的患者。

主要观察指标

皮肌炎和临床无肌病性皮肌炎的发病率以及临床无肌病性皮肌炎患者发生恶性肿瘤的风险。

结果

在识别出的29例患者中,6例(21%)患有临床无肌病性皮肌炎亚型,22例(76%)为女性。包括所有亚型在内的皮肌炎总体年龄和性别调整发病率为每100万人9.63例(95%置信区间[CI],6.09 - 13.17),临床无肌病性皮肌炎为每100万人2.08例(95% CI,0.39 - 3.77)。皮肌炎所有亚型的年龄和性别调整患病率为每10万人21.42例(95% CI,13.07 - 29.77)。8例患者(28%)在研究期间患有恶性疾病;经典皮肌炎与临床无肌病性皮肌炎相比,发生恶性肿瘤的风险(比值比)为4.61,但无统计学意义(95% CI,0.22 - 96.09)(P = 0.44)。

结论

皮肌炎是一种罕见疾病,临床无肌病性皮肌炎约占所有皮肌炎病例的20%。需要开展更大规模的基于人群的研究来估计与皮肌炎亚型相关的恶性肿瘤风险,尤其是临床无肌病性皮肌炎。