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[疱疹样皮炎:综述]

[Dermatitis herpetiformis: a review].

作者信息

Ingen-Housz-Oro S

机构信息

Service de dermatologie, hôpital Henri-Mondor, 51 avenue du Maréchal-De-Lattre-de-Tassigny, Créteil, France.

出版信息

Ann Dermatol Venereol. 2011 Mar;138(3):221-7. doi: 10.1016/j.annder.2011.01.005.

Abstract

BACKGROUND

Dermatitis herpetiformis (DH) is a rare auto-immune bullous disease characterized by its almost constant association to gluten sensitivity.

OBJECTIVE

Review of literature about epidemiology, physiopathology, clinical data and treatment of DH.

METHODS

Research on Medline and Embase database without any time limit until April 2010. Because of the lack of randomized therapeutic trials in DH, retrospective series and case reports have been analyzed.

RESULTS

DH is related to auto-antibodies against epidermal transglutaminase, which belongs to the same family as tissue transglutaminase, the auto-antigen of celiac disease. Physiopathology is complex, occurring in HLA DQ2 or DQ8 predisposed patients, and implies gluten, immunological reaction in the intestinal wall then in the skin. DH and celiac disease may be encountered in the same family. DH is characterized by a very pruritic microvesicular eruption typically located on elbows, knees and buttocks. Digestive manifestations of celiac disease occur in 15% of cases. Direct immunofluorescence is necessary to confirm the diagnosis, showing granular IgA±C3 deposits in the papillary dermis. Circulating IgA and IgG antiendomysium and antitransglutaminase antibodies are detected in almost all patients at the acute phase and follow the clinical course of the disease. Gastro-intestinal endoscopy with multiple duodenal biopsies shows partial or complete villous atrophy in two thirds of cases, intraepithelial lymphocyte infiltrate in the other cases. Other auto-immune diseases may be associated in 10-20% of cases. The main long-term risk is the occurrence of T or B nodal or intestinal tract lymphoma in 2% of cases (relative risk close to 6 in several studies, but not admitted by all authors), especially if adherence to gluten-free diet is not strict. Treatment is based on dapsone, which is quickly efficient on cutaneous manifestations, but not on the digestive involvement and on strict and definitive gluten-free diet, which cures villous atrophy and reduces the risk of lymphoma.

CONCLUSION

DH is associated to a gluten enteropathy and its physiopathology is better known. Even if the risk of secondary lymphoma seems little, most of the authors recommend a definitive gluten-free diet.

摘要

背景

疱疹样皮炎(DH)是一种罕见的自身免疫性大疱性疾病,其几乎总是与麸质敏感性相关。

目的

综述关于DH的流行病学、生理病理学、临床资料及治疗的文献。

方法

检索Medline和Embase数据库,检索时间截至2010年4月,无时间限制。由于DH缺乏随机治疗试验,因此对回顾性系列研究和病例报告进行了分析。

结果

DH与针对表皮转谷氨酰胺酶的自身抗体有关,表皮转谷氨酰胺酶与组织转谷氨酰胺酶属于同一家族,而组织转谷氨酰胺酶是乳糜泻的自身抗原。生理病理学较为复杂,发生在具有HLA DQ2或DQ8易感性的患者中,涉及麸质、肠道壁的免疫反应,进而累及皮肤。DH和乳糜泻可能在同一家族中出现。DH的特征是一种非常瘙痒的微水疱疹,通常位于肘部、膝部和臀部。乳糜泻的消化系统表现出现在15%的病例中。直接免疫荧光检查对于确诊是必要的,显示乳头真皮层有颗粒状IgA±C3沉积。在急性期,几乎所有患者都能检测到循环中的IgA和IgG抗肌内膜及抗转谷氨酰胺酶抗体,且这些抗体随疾病的临床病程变化。进行多次十二指肠活检的胃肠内镜检查显示,三分之二的病例有部分或完全绒毛萎缩,其他病例有上皮内淋巴细胞浸润。10% - 20%的病例可能合并其他自身免疫性疾病。主要的长期风险是2%的病例会发生T或B细胞淋巴瘤或肠道淋巴瘤(在几项研究中相对风险接近6,但并非所有作者都认可),尤其是在不严格遵守无麸质饮食的情况下。治疗基于氨苯砜,其对皮肤表现起效迅速,但对消化系统受累无效,同时基于严格且明确的无麸质饮食,这种饮食可治愈绒毛萎缩并降低淋巴瘤风险。

结论

DH与麸质性肠病相关,其生理病理学已得到更好的了解。即使继发淋巴瘤的风险似乎较小,但大多数作者仍推荐采用明确的无麸质饮食。

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