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一名9岁男孩幼年型无肌病性皮肌炎的节段性叠加表现

Superimposed Segmental Manifestation of Juvenile Amyopathic Dermatomyositis in a 9-year-old Boy.

作者信息

Bulur Isil, Erdogan Hilal Kaya, Saracoglu Zeynep Nurhan, Happle Rudolf, Canaz Funda

机构信息

Department of Dermatology, Faculty of Medicine, Eskisehir Osmangazi University, Eskisehir, Turkey.

Department of Dermatology, Freiburg University Medical Center, Freiburg, Germany.

出版信息

Indian J Dermatol. 2017 Jul-Aug;62(4):440. doi: 10.4103/ijd.IJD_335_16.

DOI:10.4103/ijd.IJD_335_16
PMID:28794565
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5527735/
Abstract

Dermatomyositis is a well-known autoimmune disorder. On the other hand, juvenile amyopathic dermatomyositis (JADM) occurs rather rarely. Here, we report an unusual case in a 9-year-old Turkish boy showing a unilateral linear inflammatory skin lesion that was followed, after 16 months, by the appearance of bilateral disseminated features JADM.

摘要

皮肌炎是一种众所周知的自身免疫性疾病。另一方面，青少年无肌病性皮肌炎（JADM）则较为罕见。在此，我们报告一例罕见病例，一名9岁土耳其男孩出现单侧线状炎症性皮肤病变，16个月后出现双侧播散性JADM特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4d5/5527735/b41790251d74/IJD-62-440a-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4d5/5527735/1d465b92f671/IJD-62-440a-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4d5/5527735/531d7717567d/IJD-62-440a-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4d5/5527735/b41790251d74/IJD-62-440a-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4d5/5527735/1d465b92f671/IJD-62-440a-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4d5/5527735/531d7717567d/IJD-62-440a-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4d5/5527735/b41790251d74/IJD-62-440a-g003.jpg

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本文引用的文献

1
Superimposed segmental dermatomyositis is a juvenile disorder.
Eur J Dermatol. 2014 May-Jun;24(3):291-2. doi: 10.1684/ejd.2014.2363.
2
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.
3
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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Clinical analysis of 50 children with juvenile dermatomyositis.50 例幼年型皮肌炎患儿的临床分析。
Mod Rheumatol. 2013 Mar;23(2):311-7. doi: 10.1007/s10165-012-0647-4. Epub 2012 Apr 22.
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Juvenile dermatomyositis presenting as an acquired inflammatory Blaschko-linear dermatosis.
J Am Acad Dermatol. 2011 Oct;65(4):e134-e135. doi: 10.1016/j.jaad.2011.05.044.
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A case of juvenile dermatomyositis manifesting inflammatory epidermal nevus-like skin lesions: unrecognized cutaneous manifestation of blaschkitis?一例表现为炎症性表皮痣样皮肤损害的幼年型皮肌炎：未被识别的 Blaschkitis 皮肤表现？
Allergol Int. 2010 Dec;59(4):425-8. doi: 10.2332/allergolint.10-CR-0213. Epub 2010 Oct 25.
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Superimposed segmental dermatomyositis: an emerging new paradigm.
Eur J Dermatol. 2010 Sep-Oct;20(5):551. doi: 10.1684/ejd.2010.1036. Epub 2010 Aug 24.
8
Superimposed segmental manifestation of both rare and common cutaneous disorders: a new paradigm.罕见和常见皮肤疾病的叠加节段性表现：一种新范式。
Actas Dermosifiliogr. 2009 Nov;100 Suppl 1:77-85. doi: 10.1016/s0001-7310(09)73171-0.
9
Pronounced linear calcinosis in a boy with mild dermatomyositis. A further possible example of superimposed segmental manifestation of a polygenic disorder.一名患有轻度皮肌炎的男孩出现明显的线状钙质沉着症。这是多基因疾病叠加节段性表现的另一个可能例子。
Dermatology. 2009;219(2):155-7. doi: 10.1159/000219246. Epub 2009 May 14.
10
Classification of polygenic inflammatory diseases distributed along the lines of Blaschko.
Dermatology. 2009;219(2):99-101. doi: 10.1159/000219245. Epub 2009 May 14.