Stewart M I, Woodley D T, Briggaman R A
Department of Dermatology, Stanford University School of Medicine, CA 94305.
Arch Dermatol. 1991 Mar;127(3):373-7.
Epidermolysis bullosa acquisita (EBA) is a well-characterized, subepidermal blistering disorder associated with autoimmunity to type VII collagen, which is the collagen localized to anchoring fibrils within the dermoepidermal junction of skin. Although the full clinical spectrum of EBA is still being defined, it is known that the clinical features of EBA may be reminiscent of hereditary dystrophic epidermolysis bullosa, a scarring blistering disease of children that is commonly associated with esophageal stenosis. We describe a patient with EBA who had both an acral-predominant mechanobullous disease akin to dystrophic epidermolysis bullosa and an inflammatory, widespread bullous eruption reminiscent of bullous pemphigoid in association with esophageal webs and dysphagia. Although esophageal involvement is common in dystrophic epidermolysis bullosa, a review of the literature shows that this is the first bonafide case of EBA with symptomatic esophageal disease.
获得性大疱性表皮松解症(EBA)是一种特征明确的表皮下大疱性疾病,与针对VII型胶原蛋白的自身免疫有关,VII型胶原蛋白是位于皮肤真皮表皮交界处锚定原纤维中的胶原蛋白。尽管EBA的完整临床谱仍在确定中,但已知EBA的临床特征可能使人联想到遗传性营养不良性大疱性表皮松解症,这是一种儿童瘢痕性大疱性疾病,通常与食管狭窄有关。我们描述了一名患有EBA的患者,该患者既有类似于营养不良性大疱性表皮松解症的以肢端为主的机械性大疱性疾病,又有类似于大疱性类天疱疮的炎症性、广泛的大疱性皮疹,同时伴有食管蹼和吞咽困难。尽管食管受累在营养不良性大疱性表皮松解症中很常见,但文献回顾显示,这是首例有症状性食管疾病的真正EBA病例。