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Two clinical reports and literature review of hemophagocytic syndrome
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DOI   10.11656/j.issn.1672-1519.2017.06.13
Key Words   hemophagocytic syndrome;clinical reports;traditional Chinese medicine;literature
Author NameAffiliation
HE Jing Hematological Department, First Teaching Hospital of Traditional Chinese Medicine, Tianjin 300193, China 
ZENG Li-rong Teaching and Research Section of Typhoid Fever, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China 
GAO Hong Hematological Department, First Teaching Hospital of Traditional Chinese Medicine, Tianjin 300193, China 
SHI Zhe-xin Hematological Department, First Teaching Hospital of Traditional Chinese Medicine, Tianjin 300193, China 
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.

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