haemophagocytic造句

• The most common histiocyte disorders are Langerhans'cell histiocytosis and haemophagocytic lymphohistiocytosis.
• Type 2 have mutations in RAB27A and haemophagocytic syndrome, with abnormal T-cell and macrophage activation.
• Secondary haemophagocytic lymphohistiocytosis ( acquired haemophagocytic lymphohistiocytosis ) occurs after strong immunologic activation, such as that which can occur with systemic infection, immunodeficiency, or underlying malignancy.
• Secondary haemophagocytic lymphohistiocytosis ( acquired haemophagocytic lymphohistiocytosis ) occurs after strong immunologic activation, such as that which can occur with systemic infection, immunodeficiency, or underlying malignancy.
• Primary HLH, also known as "'familial haemophagocytic lymphohistiocytosis "'( FHL ) or familial erythrophagocytic lymphohistiocytosis, is a heterogeneous autosomal recessive disorder found to be more prevalent with parental consanguinity.