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hemophagocytic lymphohistiocytosis : ウィキペディア英語版
hemophagocytic lymphohistiocytosis

Hemophagocytic lymphohistiocytosis (HLH), also known as haemophagocytic lymphohistiocytosis (British spelling), and hemophagocytic or haemophagocytic syndrome, is an uncommon hematologic disorder. It is a life-threatening disease of severe hyperinflammation caused by uncontrolled proliferation of activated lymphocytes and macrophages characterised 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.
==History==
The first case report of HLH was published in 1952.(Farquhar and Claireaux )

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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