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Two clinical reports and literature review of hemophagocytic syndrome |
Hits 1655 Download times 1270 Received:May 10, 2017 |
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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 Name | Affiliation | 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 |
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Abstract
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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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