Erdheim–Chester disease (ECD) is a disease of non-Langerhans cell histiocyte
multisystemic proliferation. The pathogenesis is related to accumulation of histiocytes across …

Erdheim-Chester disease (ECD) is a rare, non-Langerhans cell histiocytosis of unknown
etiology, characterized by multiple organ involvement. Erdheim-Chester disease is usually …

History A 61-year-old man with no relevant medical history was admitted to the emergency
department with symptoms of congestive heart failure and a 1-week history of chest pain …

Abstract Background Erdheim-Chester disease (ECD) is a rare, non-Langerhans cell
histiocytosis with characteristic radiological and histological features. This entity is defined …

Erdheim‑Chester disease (ECD) is a rare tumor of histiocytic origin, characterized by foamy
or lipid‑laden histiocytes mixed or surrounded by fibrosis that infiltrate multiple organs …

Discussion: Erdheim-Chester Disease (ECD) is a multisystemic non-Langerhans cell
histiocytic disorder seen in adults between 40 and 70 years [1], which manifests with diverse …

Abstract Introduction: Erdheim-Chester disease (ECD) is an uncommon non-Langerhans
cell histiocytosis. Bilateral symmetric sclerosis of the long bones and probable multiorgan …

Erdheim-Chester disease (ECD) is a rare histiocytic disease that affects multiple systems in
the body. While it typically targets long bones, cardiovascular structures, the …

Abstract Background Erdheim–Chester disease (ECD) is a rare non-Langerhans cell
histiocytosis that can affect the bones, heart, lungs, brain, and other organs. Cardiovascular …

Erdheim-Chester disease (ECD) is a rare non-Langerhans cell histiocytic disorder. The
diagnosis was based on the relationship between radiologic findings, clinical …