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青少年临床无肌病性皮肌炎:一例报告及文献复习

Juvenile Clinically Amyopathic Dermatomyositis: A Case Report and Review of Literature.

作者信息

Javadi Parvaneh Vadood, Yasaei Mehrdad, Rahmani Khosro, Nilipour Yalda

机构信息

Department of Rheumatology, Mofid Children's Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Pediatric Pathology Research Center, Mofid Children's Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

出版信息

Iran J Child Neurol. 2019 Summer;13(3):113-120.

PMID:31327976
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6586448/
Abstract

Juvenile clinically amyopathic dermatomyositis (juvenile CADM) is a rare rheumatologic disease in children defined as the presence of the hallmark cutaneous features of dermatomyositis in absence of muscle involvement In this article, we report an Iranian 14.5-year-old girl presented to Rheumatology Clinic of Mofid Children's Hospital, Tehran, Iran in Jan 2016 with cutaneous complaints diagnosed with juvenile CADM. Finally, we provide a literature review of previous studies on juvenile CADM.

摘要

青少年临床无肌病性皮肌炎(juvenile CADM)是一种罕见的儿童风湿性疾病,定义为存在皮肌炎的典型皮肤特征但无肌肉受累。在本文中,我们报告了一名14.5岁的伊朗女孩,于2016年1月前往伊朗德黑兰莫菲德儿童医院的风湿病诊所,因皮肤问题就诊,被诊断为青少年CADM。最后,我们对以往关于青少年CADM的研究进行了文献综述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/868c/6586448/1eb0284d0f80/ijcn-13-113-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/868c/6586448/0345e48ec2b5/ijcn-13-113-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/868c/6586448/214306c5ee85/ijcn-13-113-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/868c/6586448/1eb0284d0f80/ijcn-13-113-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/868c/6586448/0345e48ec2b5/ijcn-13-113-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/868c/6586448/214306c5ee85/ijcn-13-113-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/868c/6586448/1eb0284d0f80/ijcn-13-113-g003.jpg

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本文引用的文献

1
Treatment of clinically amyopathic dermatomyositis in adults: a systematic review.成人临床无肌病性皮肌炎的治疗:系统评价。
Br J Dermatol. 2018 Dec;179(6):1248-1255. doi: 10.1111/bjd.14726. Epub 2016 Aug 30.
2
Diagnosis and treatment of clinically amyopathic dermatomyositis (CADM): a case series and literature review.临床无肌病性皮肌炎(CADM)的诊断与治疗:病例系列报道及文献综述
Clin Rheumatol. 2016 Aug;35(8):2125-2130. doi: 10.1007/s10067-015-2928-8. Epub 2015 Apr 7.
3
Clinical and laboratory features of fatal rapidly progressive interstitial lung disease associated with juvenile dermatomyositis.
与青少年皮肌炎相关的致命性快速进展性间质性肺疾病的临床和实验室特征
Rheumatology (Oxford). 2015 May;54(5):784-91. doi: 10.1093/rheumatology/keu385. Epub 2014 Oct 6.
4
A hyper-ferritinemia syndrome evolving in recurrent macrophage activation syndrome, as an onset of amyopathic juvenile dermatomyositis: a challenging clinical case in light of the current diagnostic criteria.一种以反复发作性巨噬细胞活化综合征为表现的高铁蛋白血症综合征,为无肌病性皮肌炎的首发表现:当前诊断标准下的一个具有挑战性的临床病例。
Autoimmun Rev. 2014 Nov;13(11):1142-8. doi: 10.1016/j.autrev.2014.05.009. Epub 2014 May 29.
5
Juvenile hypomyopathic dermatomyositis initiating with acquired inflammatory Blaschko-linear dermatosis.
Eur J Dermatol. 2014 May-Jun;24(3):395-6. doi: 10.1684/ejd.2014.2327.
6
Common and distinct clinical features in adult patients with anti-aminoacyl-tRNA synthetase antibodies: heterogeneity within the syndrome.抗氨酰基-tRNA 合成酶抗体的成年患者的常见和独特临床特征:综合征内的异质性。
PLoS One. 2013;8(4):e60442. doi: 10.1371/journal.pone.0060442. Epub 2013 Apr 3.
7
Brief report: Association of HLA-DRB1*0101/*0405 with susceptibility to anti-melanoma differentiation-associated gene 5 antibody-positive dermatomyositis in the Japanese population.简短报告:在日本人群中,HLA - DRB1*0101/*0405与抗黑色素瘤分化相关基因5抗体阳性皮肌炎易感性的关联
Arthritis Rheum. 2012 Nov;64(11):3736-40. doi: 10.1002/art.34657.
8
Anti-CADM-140/MDA5 autoantibody titer correlates with disease activity and predicts disease outcome in patients with dermatomyositis and rapidly progressive interstitial lung disease.抗 CADM-140/MDA5 自身抗体滴度与皮肌炎和快速进展性间质性肺病患者的疾病活动度相关,并可预测疾病结局。
Mod Rheumatol. 2013 May;23(3):496-502. doi: 10.1007/s10165-012-0663-4. Epub 2012 May 29.
9
Clinical manifestations of dermatomyositis and clinically amyopathic dermatomyositis patients with positive expression of anti-melanoma differentiation-associated gene 5 antibody.抗黑色素瘤分化相关基因 5 抗体阳性的皮肌炎和临床无肌病性皮肌炎患者的临床表现。
Arthritis Care Res (Hoboken). 2012 Oct;64(10):1602-10. doi: 10.1002/acr.21728.
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Disappearance of anti-MDA-5 autoantibodies in clinically amyopathic DM/interstitial lung disease during disease remission.在临床无肌病性皮肌炎/间质性肺病缓解期间,抗 MDA-5 自身抗体消失。
Rheumatology (Oxford). 2012 May;51(5):800-4. doi: 10.1093/rheumatology/ker408. Epub 2011 Dec 30.