摘要
噬血细胞综合征(hemophagocytic syndrome, HPS)又称噬血细胞性淋巴组织细胞增生症(hemophagocytic lymphphistiocysis, HLH)是一种过度炎症反应综合征。即使在适当的治疗下死亡率仍高[1]。分为两大类,即原发性和继发性HPS[2],现将我院2013年诊治的2例继发性HPS报告如下。
出处
《罕少疾病杂志》
2014年第3期51-53,共3页
Journal of Rare and Uncommon Diseases
参考文献9
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共引文献7
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同被引文献6
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