
Hemophagocytic lymphohistiocytosis with high serum levels of IL-18 and predominant lymphocyte activation in a neonate born to a mother with adult-onset Still's disease
Keywords: فعال سازی لنفوسیت; HLH; hemophagocytic lymphohistiocytosis; CTL; cytotoxic T lymphocytes; FHL; familial HLH; MAS; macrophage activation syndrome; AOSD; adult-onset Still's disease; sJIA; systemic-onset juvenile idiopathic arthritis; NK; natural killer; IL; interleukin; sIL2