天津中医药2017，Vol.34Issue(6)：400-402,3.DOI:10.11656/j.issn.16721519.2017.06.13
噬血细胞综合征2例临床报告及文献复习
Two clinical reports and literature review of hemophagocytic syndrome
何敬 1曾丽蓉 2高宏 1史哲新1
作者信息
- 1. 天津中医药大学第一附属医院血液科,天津 300193
- 2. 天津中医药大学伤寒教研室,天津 300193
- 折叠
摘要
Abstract
Hemophagocytic lymphohistiocytosis (HLH), also known as hemophagocytic syndrome, is an uncommon hematologic disorder. It is a life-threatening disease of severe hyperinflammation caused by uncontrolled proliferation of activated lymphocytes and macrophages, characterized by proliferation of morphologically benign lymphocytes and macrophages that secrete high amounts of inflammatory cytokines. It is classified as one of the cytokine storm syndromes. In this article, two clinical cases of our department were reported. Combined with literature review, it was analyzed the thinking way of diagnosing and treating.关键词
嗜血细胞综合征/临床报告/中医/文献Key words
hemophagocytic syndrome/clinical reports/traditional Chinese medicine/literature分类
医药卫生引用本文复制引用
何敬,曾丽蓉,高宏,史哲新..噬血细胞综合征2例临床报告及文献复习[J].天津中医药,2017,34(6):400-402,3.
