Department of Pediatrics, Mother and Child Health Institute Dr Vukan Cupic, University of Belgrade, Faculty of Medicine and University of Kragujevac, Faculty of Medicine, Serbia.
Indian Pediatr. 2012 Aug;49(8):672-4.
We report the successful use of rituximab as single treatment modality in a five-month-old boy with fulminant warm autoantibody autoimmune hemolytic anemia, resistant to standard treatment. On admission, laboratory tests showed a profound anemia with a hemoglobin of 2.6 g/dL. Indirect and direct antiglobulin tests were strongly positive, and nonspecific IgG autoantibodies were detected. Two days of intravenous corticosteroids (methylprednisolone 4mg/kg) and immunoglobulins (1g/kg) did not halt the hemolysis and the infant was severely transfusion-dependent. Rituximab 375mg/sq m weekly was given for 4 weeks, the hepatosplenomegaly gradually regressed, the lymphocytes normalized and he is free from hemolysis two years after treatment.
我们报告了一例 5 月龄男婴暴发性温自身抗体自身免疫性溶血性贫血,对标准治疗耐药,成功使用利妥昔单抗作为单一治疗方法。入院时,实验室检查显示严重贫血,血红蛋白为 2.6g/dL。间接和直接抗球蛋白试验均呈强阳性,检测到非特异性 IgG 自身抗体。静脉注射皮质类固醇(甲泼尼龙 4mg/kg)和免疫球蛋白(1g/kg)治疗 2 天未能阻止溶血,婴儿严重依赖输血。给予利妥昔单抗 375mg/㎡,每周一次,共 4 周,肝脾肿大逐渐消退,淋巴细胞恢复正常,治疗 2 年后无溶血。