What is another word for hemophagocytic syndrome?
Pronunciation: [hˌiːməfˌaɡəsˈɪtɪk sˈɪndɹə͡ʊm] (IPA) 
Hemophagocytic syndrome, also known as hemophagocytic lymphohistiocytosis (HLH), is a rare autoimmune disorder characterized by hyperinflammation and excessive immune activation. Some synonyms for this condition include hemophagocytic histiocytosis, hemophagocytic lymphohistiocytosis syndrome, and reactive histiocytosis. HLH can present as a primary genetic disorder or secondary to other conditions like infections, autoimmune diseases, or malignancies. Its symptoms include fever, hepatosplenomegaly, cytopenias, and hyperferritinemia. Early diagnoses and treatments are crucial for HLH management. Clinicians may utilize chemotherapy, immunosuppressive therapies, or stem cell transplants. Increased awareness and understanding of HLH can lead to better patient outcomes.
