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本文引用的文献

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Dermatitis herpetiformis. Part II. Diagnosis, management, and prognosis.疱疹样皮炎。第二部分。诊断、治疗和预后。
J Am Acad Dermatol. 2011 Jun;64(6):1027-33; quiz 1033-4. doi: 10.1016/j.jaad.2010.09.776.
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Dermatitis herpetiformis. Part I. Epidemiology, pathogenesis, and clinical presentation.疱疹样皮炎。第一部分。流行病学、发病机制和临床表现。
J Am Acad Dermatol. 2011 Jun;64(6):1017-24; quiz 1025-6. doi: 10.1016/j.jaad.2010.09.777.
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Detection of antibodies to epidermal transglutaminase but not tissue transglutaminase in Japanese patients with dermatitis herpetiformis.日本疱疹样皮炎患者中表皮转谷氨酰胺酶而非组织转谷氨酰胺酶抗体的检测
Br J Dermatol. 2011 Apr;164(4):883-4. doi: 10.1111/j.1365-2133.2010.10153.x. Epub 2011 Mar 10.
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Fibrillar IgA deposition in dermatitis herpetiformis--an underreported pattern with potential clinical significance.疱疹样皮炎中的纤维状IgA沉积——一种报道不足但具有潜在临床意义的模式。
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Prevalence of celiac disease in the Asia-Pacific region.亚太地区乳糜泻的患病率。
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IgA anti-epidermal transglutaminase antibodies in dermatitis herpetiformis and pediatric celiac disease.疱疹样皮炎和小儿乳糜泻中的IgA抗表皮转谷氨酰胺酶抗体
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Guidelines for the diagnosis and treatment of dermatitis herpetiformis.疱疹样皮炎诊断和治疗指南。
J Eur Acad Dermatol Venereol. 2009 Jun;23(6):633-8. doi: 10.1111/j.1468-3083.2009.03188.x. Epub 2009 Mar 10.
8
Autoantibodies against epidermal transglutaminase are a sensitive diagnostic marker in patients with dermatitis herpetiformis on a normal or gluten-free diet.在正常饮食或无麸质饮食的疱疹样皮炎患者中,抗表皮转谷氨酰胺酶自身抗体是一种敏感的诊断标志物。
J Am Acad Dermatol. 2009 Jul;61(1):39-43. doi: 10.1016/j.jaad.2008.12.037. Epub 2009 Apr 2.
9
Clinical, pathologic, and immunopathologic features of dermatitis herpetiformis: review of the Mayo Clinic experience.疱疹样皮炎的临床、病理及免疫病理特征:梅奥诊所经验回顾
Int J Dermatol. 2007 Sep;46(9):910-9. doi: 10.1111/j.1365-4632.2007.03214.x.
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Transglutaminase autoantibodies in dermatitis herpetiformis and celiac sprue.疱疹样皮炎和乳糜泻中的转谷氨酰胺酶自身抗体。
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日本疱疹样皮炎的独特特征:对过去35年中91例日本患者的回顾

Distinct characteristics in Japanese dermatitis herpetiformis: a review of all 91 Japanese patients over the last 35 years.

作者信息

Ohata Chika, Ishii Norito, Hamada Takahiro, Shimomura Yutaka, Niizeki Hironori, Dainichi Teruki, Furumura Minao, Tsuruta Daisuke, Hashimoto Takashi

机构信息

Department of Dermatology, Kurume University School of Medicine, 67 Asahimachi, Kurume, Fukuoka 830-0011, Japan.

出版信息

Clin Dev Immunol. 2012;2012:562168. doi: 10.1155/2012/562168. Epub 2012 Jun 12.

DOI:10.1155/2012/562168
PMID:22778765
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3385876/
Abstract

We reviewed all 91 Japanese dermatitis herpetiformis (DH) patients reported over the last 35 years. The male-to-female ratio was 2 : 1. The mean age at onset was 43.8, and 13 years earlier for female patients. More than half of these Japanese DH patients showed granular IgA deposition in the papillary dermis, and another one-third showed fibrillar IgA deposition. The male patients with granular IgA deposition were 10 years older than those with fibrillar deposition. Whereas patients with granular IgA deposition showed typical distribution of the skin lesions, the predilection sites of DH tended to be spared in patients with fibrillar IgA deposition. Only 3 patients had definite gluten-sensitive enteropathy. There was a statistical difference in the frequency of human leukocyte antigen (HLA)-DR9 between the granular group and controls among Japanese. No patients had HLA-DQ2 or -DQ8, which is frequently found in Caucasian DH patients. The absence of HLA-DQ2/DQ8, the inability to identify celiac disease in most cases, the predominance of fibrillar IgA, and the unusual distribution of clinical lesions in Japanese patients suggest that Japanese DH may be a subset of DH patients and have a pathogenesis which is different from that currently proposed in Caucasian DH patients.

摘要

我们回顾了过去35年里报告的所有91例日本疱疹样皮炎(DH)患者。男女比例为2∶1。发病的平均年龄为43.8岁,女性患者则早13年。这些日本DH患者中,超过一半在乳头真皮层显示颗粒状IgA沉积,另有三分之一显示纤维状IgA沉积。颗粒状IgA沉积的男性患者比纤维状沉积的患者大10岁。颗粒状IgA沉积的患者表现出典型的皮损分布,而纤维状IgA沉积的患者DH的好发部位往往未受累。只有3例患者有明确的麸质敏感性肠病。在日本人中,颗粒状组与对照组之间人类白细胞抗原(HLA)-DR9的频率存在统计学差异。没有患者有HLA-DQ2或-DQ8,而这在白种人DH患者中经常发现。日本患者缺乏HLA-DQ2/DQ8、大多数病例中无法识别乳糜泻、纤维状IgA占优势以及临床皮损分布异常,提示日本DH可能是DH患者的一个子集,其发病机制与目前白种人DH患者中提出的不同。