Porcaro F, Valenzise M, Candela G, Chiera F, Corica D, Pitrolo E, Santucci S, Romeo M, Nigro S, Zirilli G
Department of Pediatrics, University of Messina, Messina.
Pediatr Med Chir. 2014 Aug 31;36(4):91. doi: 10.4081/pmc.2014.91.
We describe a case of a 14-years old caucasian female affected by autoimmune hemolytic anemia and thrombocytopenia successfully treated with intravenous immunoglobulin and steroids. Nevertheless, neutropenia occurred during follow-up period. Positivity of direct antiglobulin test and sieric anti-neutrophil antibodies suggested the diagnosis of Evans syndrome trilineage.
我们描述了一例14岁的白种女性患者,患有自身免疫性溶血性贫血和血小板减少症,通过静脉注射免疫球蛋白和类固醇成功治疗。然而,在随访期间出现了中性粒细胞减少症。直接抗球蛋白试验阳性和血清抗中性粒细胞抗体提示诊断为全血细胞减少型伊文氏综合征。