A case of Erdheim-Chester disease which affected the epiphysis and showed evidence of systemic disease is presented. Clinical and histopathological similarities with other forms of disseminated Langerhans' cell histiocytosis are noted, particularly reaction of infiltrating histiocytes for S100 and HLA-DR.
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Online ISSN 1472-4146
Copyright © 2012 by the BMJ Publishing Group Ltd & Association of Clinical Pathologists. All rights reserved.
