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继发性嗜血性淋巴细胞增生症治疗进展 被引量:1

Treatment of Secondary Hemophagocytic Lymphohsitiocytosis Syndrome
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摘要 继发性嗜血性淋巴组织细胞增生症(SHLH)是一组单核/巨噬细胞系统异常活化导致的致死性疾病,多继发于感染、恶性肿瘤、风湿性疾病等。SHLH预后与原发病有很大的关系。在引入HLH-94及随后的HLH-04方案后,SHLH预后有了明显的改善。SHLH的治疗取决于原发病的性质和病情,严重者采用自体骨髓移植有望治愈。 Secondary hemophagocytic lymphohsitiocytosis(SHLH)is a series of fatal diseases resulted from abnormally activated monocyte/macrophage system,which is often secondary to infection,malignancy tumor,and rheumatic disease.SHLH prognosis is greatly related with the primary disease.After the introduction of HLH-94 and HLH-04 solution,prognosis of SHLH has been improved significantly,while the treatment for SHLH depends on the nature and condition of the primary disease,auto bone marrow transplantation is a hope for the cure of severe cases.
作者 彭玲 尹晓林
出处 《医学综述》 2012年第3期392-394,共3页 Medical Recapitulate
关键词 嗜血性淋巴细胞增生症 继发性 治疗 Hemophagocytic lymphohistiocytosis Secondary Treatment
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参考文献29

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