Kühne U, Marsch W C
Zentrum der Dermatologie und Venerologie, Johann Wolfgang Goethe-Universität, Frankfurt am Main, Germany.
Acta Derm Venereol. 1991;71(1):83-4.
A 59-year-old patient suffered from persistent angioedema-like swellings and blood eosinophilia. The disease was preceded by an erythema multiforme-like exanthema and urticarial papules. Persistent eosinophilia with exclusion of its known causes and skin biopsy helped to establish the diagnosis of the benign variant of hypereosinophilic syndrome known as 'episodic angioedema with eosinophilia'. Corticosteroid therapy was successful. The therapeutic alternatives are discussed.
一名59岁患者患有持续性血管性水肿样肿胀和血液嗜酸性粒细胞增多。该疾病之前有多形红斑样皮疹和荨麻疹丘疹。排除已知病因后的持续性嗜酸性粒细胞增多以及皮肤活检有助于确诊为高嗜酸性粒细胞综合征的良性变异型，即“伴有嗜酸性粒细胞增多的发作性血管性水肿”。皮质类固醇治疗取得成功。文中讨论了其他治疗选择。
