嗜血细胞综合征(hemophagocytic syndrome,HPS)是指在细菌或病毒感染时,于骨髓和淋巴结内发生的成熟组织细胞的自限性增生,吞噬现象明显,于1979年由Risdall等首先报道,属反应性组织细胞增生症的一种特殊类型。现将本院所见的2例报告如下。1病例报告例1女,13岁。因面色、口唇苍白,双下肢浮肿,精神差就诊。查 Hemophagocytic syndrome (hemophagocytic syndrome, HPS) refers to self-limiting hyperplasia and phagocytosis of mature tissue cells occurring in the bone marrow and lymph nodes during bacterial or viral infection. It was first reported by Risdall et al in 1979 as a reaction A special type of histiocytosis. Now see this hospital 2 cases are as follows. 1 case report 1 female, 13 years old. Due to complexion, pale lips, lower extremity edema, mental poor treatment. check