A rare form of non-Langerhans-cell histiocytosis (histiocytosis, non-langerhans-cell) with onset in middle age. The systemic disease is characterized by infiltration of lipid-laden macrophages, multinucleated giant cells, an inflammatory infiltrate of lymphocytes and histiocytes in the bone marrow, and a generalized sclerosis of the long bones.


Leave a message about 'Erdheim-Chester Disease'

We do not evaluate or guarantee the accuracy of any content in this site. Click here for the full disclaimer.