hemophagocytic lymphohistiocytosis

Hemophagocytic Lymphohistiocytosis

Hemophagocytic Disorder

HLH

A rare, but potentially life-threatening disorder, characterized by the proliferation of histiocytes and macrophages, and phagocytosis of red blood cells, white blood cells, and platelets. It may be inherited or secondary due to infections, autoimmune disorders, or underlying malignancies. Signs and symptoms include fever, lymphadenopathy, hepatomegaly, splenomegaly, and pancytopenia.

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C34792

A rare disorder in which histiocytes and lymphocytes (types of white blood cells) build up in organs including the skin, spleen, and liver, and destroy other blood cells. Hemophagocytic lymphohistiocytosis may be inherited or caused by certain conditions or diseases, including infections, immunodeficiency (inability of the body to fight infections), and cancer.

C34792

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C116977

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C118168

CTRP

A rare, but potentially life-threatening disorder, characterized by the proliferation of histiocytes and macrophages, and phagocytosis of red blood cells, white blood cells, and platelets. It may be inherited or secondary due to infections, autoimmune disorders, or underlying malignancies. Signs and symptoms include fever, lymphadenopathy, hepatomegaly, splenomegaly, and pancytopenia.

Hemophagocytic Lymphohistiocytosis

hemophagocytic lymphohistiocytosis

Hemophagocytic Lymphohistiocytosis

Hemophagocytic Disorder

HLH

Hemophagocytic Lymphohistiocytosis

Hemophagocytic_Lymphohistiocytosis

Haemophagocytic lymphohistiocytosis

Hemophagocytic Lymphohistiocytosis

Thesaurus:C34792

Disease or Syndrome

C3554542

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C26324

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C203422

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C53543