Jansen T, Küppers U, Plewig G
Hautklinik, Heinrich-Heine-Universität, Düsseldorf.
Hautarzt. 1992 Jul;43(7):426-31.
In 1937, Sulzberger and Garbe singled out an exudative discoid and lichenoid chronic dermatosis characterized by the combination of various symptoms which by themselves are not specific from the heterogeneous eczema group. The report of a 7-year-old girl is used as a basis to describe the characteristics of the disease and to present the authors' own interpretation. Clinically, there were discoid and lichenoid lesions with severe pruritus. Blood examination revealed eosinophilia. Histopathological examination of skin lesions showed psoriasiform, spongiotic, lichenoid dermatitis. A therapeutic regimen of oral corticosteroids led to complete regression of the skin changes. We feel that there are no clinical or histological findings to differentiate Sulzberger-Garbe disease definitely from extensive nummular eczema.
1937年，苏尔茨贝格尔和加贝指出了一种渗出性盘状和苔藓样慢性皮肤病，其特征是具有各种症状的组合，这些症状本身在异质性湿疹组中并无特异性。以一名7岁女孩的病例报告为基础来描述该病的特征并阐述作者自己的解读。临床上，有盘状和苔藓样皮损伴严重瘙痒。血液检查显示嗜酸性粒细胞增多。皮肤病变的组织病理学检查显示为银屑病样、海绵状、苔藓样皮炎。口服皮质类固醇的治疗方案使皮肤病变完全消退。我们认为，没有临床或组织学发现能够明确地将苏尔茨贝格尔 - 加贝病与广泛的钱币状湿疹区分开来。
