Stahl Lea-Sophie, Wolters Ann-Christin, Kautz Ocko, Patsinakidis Nikolaos, Raap Ulrike
Abteilung für experimentelle Allergologie und Immundermatologie, Carl von Ossietzky Universität Oldenburg, Oldenburg, Deutschland.
Universitätsklinik für Dermatologie und Allergologie, Klinikum Oldenburg AöR, Rahel-Straus-Str. 10, 26133, Oldenburg, Deutschland.
Dermatologie (Heidelb). 2022 Dec;74(12):970-973. doi: 10.1007/s00105-023-05216-4. Epub 2023 Sep 20.
A 50-year-old female farmer was initially diagnosed with generalized granuloma annulare and treated with local steroids and ultraviolet (UV) light therapy for 10 years, albeit without success. A histopathological examination in our clinic changed the diagnosis to Wells' syndrome, based on the typical findings of eosinophilic cellulitis together with flame figures. A systemic approach with pulse steroid therapy resulted in complete remission of pruritus and skin manifestations. This case demonstrates successful treatment of a patient with eosinophilic cellulitis.
一名50岁的女性农民最初被诊断为泛发性环状肉芽肿,并接受了局部类固醇和紫外线光疗10年,但未成功。在我们诊所进行的组织病理学检查根据嗜酸性粒细胞性蜂窝织炎的典型表现及火焰状图形将诊断改为威尔斯综合征。采用脉冲类固醇疗法的全身治疗方法使瘙痒和皮肤表现完全缓解。该病例证明了嗜酸性粒细胞性蜂窝织炎患者的成功治疗。