S Laugier Robiolle

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CONTEXT Erdheim-Chester disease (ECD) is a rare non-Langerhans cell histiocytosis, characterized by infiltration of foamy histiocytes in multiple organs. Endocrine involvement has mostly been described in case reports. OBJECTIVE We performed systematic endocrine evaluation in a large cohort of patients with ECD. DESIGN This was a single-center(More)
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