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作 者:陈玉秀[1] 张惠君[1] 常红[1] 吴蒙[1] 张秋业[1]
机构地区:[1]青岛大学医学院附属医院儿科,山东青岛266003
出 处:《现代生物医学进展》2013年第24期4759-4762,共4页Progress in Modern Biomedicine
摘 要:目的:探讨噬血细胞综合征患儿的临床特征、治疗及预后。方法:对38例噬血细胞综合征患儿的临床症状、体征、试验检查结果、治疗及预后,进行回顾性总结与分析。结果:38例患儿主要表现为发热、肝脾淋巴结肿大、外周血细胞减少、铁蛋白升高、凝血功能异常;经针对性治疗后,治愈3例,好转20例,疗效不佳自动出院9例,死亡6例。结论:噬血细胞综合征病因复杂,临床表现多种多样,病情凶险,预后较差,早期诊断及治疗对预后十分关键。Objective: To investigate the clinical characteristics, treatments and prognosis of children with hemophargocytic synd- rome. Methods: Aretrospective summary was performed, and the clinical symptoms, signs, laboratory test results, treatments and progno- sis of 38 cases of childhood hemophargocytic syndrome were analyzed. Results: The main manifestations included fever, enlargement of liver and spleen lymph nodes, reduction of peripheral blood cells, increase offerritin, coagulant function abnormality. After the specific treatments, 3 patients cured, 20 patients improved,9 patients discharged voluntarily due to poor efficacy, 6 patients died. Conclusion: Hemophagocytic syndrome has complicated causes, diverse clinical manifestations, dangerous conditions and poor prognosis. Early diagnosis and treatment are very critical to the prognosis.
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