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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.

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。

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