Secondary hemophagocytic lymphohistiocytosis Secondary hemophagocytic lymphohistiocytosis (secondary HLH) also known as acquired hemophagocytic lymphohistiocytosis (acquired HLH) is a rare life-threatening intense immune activation syndrome in which
Familial hemophagocytic lymphohistiocytosis Familial hemophagocytic lymphohistiocytosis (FHL) also called primary hemophagocytic lymphohistiocytosis is a rare, genetic inborn errors of immunity causing aggressive life-threatening intense immune
Hemophagocytic lymphohistiocytosis Hemophagocytic lymphohistiocytosis also called HLH syndrome is a rare, life-threatening intense immune activation syndrome in which your body makes too many activated immune cells
Rosai Dorfman disease Rosai-Dorfman disease (RDD) also called Rosai-Dorfman-Destombes disease or sinus histiocytosis with massive lymphadenopathy (SHML), is a rare benign non-Langerhans cell histiocytosis which is
Erdheim–Chester disease Erdheim-Chester disease (ECD) also known as lipid granulomatosis or polyostotic sclerosing histiocytosis, is a rare slow-growing blood cancer, a non-Langerhans cell histiocytosis neoplasm, which
What is Langerhans cell histiocytosis Langerhans cell histiocytosis (LCH) previously referred to as Hand‐Schuller‐Christian disease, Letterer‐Siwe disease, eosinophilic granuloma or histiocytosis X, is a rare
What is eosinophilic granuloma Eosinophilic granuloma now known as Langerhans cell histiocytosis, is a group of rare disorders in which too many Langerhans cells (a