Aydog Ece, Yesilli Okan, Sever Aslihan, Usan Hicran
Department of Physical Medicine and Rehabilitation, Health Ministry, Ankara Diskapi, Education and Research Hospital, Hosdere Caddesi, 23/14, Ankara, Turkey.
Saudi Med J. 2006 Jun;27(6):881-4.
Dermatitis herpetiformis DH is a rare, intensely pruritic, chronic, recurrent, papulovesicular disease. The disease can be clearly distinguished from the other subepidermal blistering eruptions by histologic, immunologic, and gastrointestinal criteria. Most patients have an associated gluten-sensitive enteropathy GSE that is usually asymptomatic. Both enteropathy and the dermatologic findings disappear with a gluten-free diet, therefore, DH is thought to be the specific dermatologic finding of celiac disease CD. An association between CD and autoimmune disease has been documented in several studies. Similar associations have been reported in DH. We report a 46-year-old man with DH diagnosed more than 10 years previously who developed GSE, pernicious anemia, and rheumatoid arthritis in the following years.
疱疹样皮炎(DH)是一种罕见的、剧烈瘙痒的慢性复发性丘疹水疱性疾病。通过组织学、免疫学和胃肠道标准,该疾病可与其他表皮下水疱性皮疹明确区分。大多数患者伴有通常无症状的麸质敏感性肠病(GSE)。肠病和皮肤病学表现均可通过无麸质饮食消失,因此,DH被认为是乳糜泻(CD)的特异性皮肤病学表现。多项研究记录了CD与自身免疫性疾病之间的关联。DH中也报道了类似的关联。我们报告一名46岁男性,10多年前被诊断为DH,在接下来的几年中发展为GSE、恶性贫血和类风湿性关节炎。