Roth R R, Smith K J, James W D
Department of Surgery, US Air Force Regional Hospital, Elmendorf AFB, Alaska.
Arch Dermatol. 1990 Sep;126(9):1191-4.
Inherited epidermolysis bullosa encompasses many subsets of diseases, distinguished by skin fragility and blister formation after minor trauma. Histologically, epidermolysis bullosa usually presents as bullae without inflammatory cells. We present four cases of epidermolysis bullosa, including examples of epidermolytic, junctional, and dermolytic types that have eosinophilic infiltrates. These cases do not represent subtypes of epidermolysis bullosa, but simply the influx of eosinophils in neonatally manifested disease. Several hypotheses for the presence of these eosinophils are presented.
遗传性大疱性表皮松解症包括许多疾病亚型,其特征为轻微创伤后皮肤脆弱并形成水疱。组织学上,大疱性表皮松解症通常表现为无炎症细胞的大疱。我们报告了4例大疱性表皮松解症病例,包括表皮松解型、交界型和真皮松解型且伴有嗜酸性粒细胞浸润的病例。这些病例并不代表大疱性表皮松解症的亚型,而仅仅是新生儿期疾病中嗜酸性粒细胞的浸润。文中提出了关于这些嗜酸性粒细胞存在的几种假说。