Weber L, Blanke H, Rodermund O E
Hautarzt. 1982 Aug;33(8):411-5.
Two patients are described having a bullous variant of angiolymphoid hyperplasia with eosinophilia on the head. This disease is characterized by inflammatory, infiltrated, plaque-like lesions with recurring bullous eruptions. At the same time there may be prurigo-like papules on the trunk and arms. The course is a characteristic histological pattern revealing cutaneous lymphocytic infiltrate, lymphoid follicle formation, and atypical vascular proliferation associated with tissue eosinophilia. Blister formation takes place subepidermally.
描述了两名头部患有嗜酸性粒细胞增多性血管淋巴样增生大疱变体的患者。这种疾病的特征是炎症性、浸润性、斑块状病变伴反复出现的大疱性皮疹。同时，躯干和手臂上可能出现痒疹样丘疹。病程具有特征性的组织学模式，表现为皮肤淋巴细胞浸润、淋巴滤泡形成以及与组织嗜酸性粒细胞增多相关的非典型血管增生。水疱形成发生在表皮下。
