拉莫三嗪
噬血细胞性淋巴组织细胞增多症
医学
地塞米松
免疫失调
免疫系统
免疫学
儿科
内科学
精神科
癫痫
疾病
作者
Hong Wang,Jing Peng,Wenbin Zeng,Xueyi Pan
出处
期刊:Clinical Laboratory
[Clinical Laboratory Publications]
日期:2024-01-01
卷期号:70 (02/2024)
被引量:2
标识
DOI:10.7754/clin.lab.2023.230730
摘要
Hemophagocytic lymphohistiocytosis (HLH) is a severe inflammatory reaction syndrome caused by genetic or acquired immune dysregulation. The majority of adult HLH cases are caused by tumors, rheumatic immune disorders, and infections. However, drug-induced HLH is rarely reported.
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