Erdheim-Chester Disease
Abstract
Erdheim-Chester disease (ECD) is a rare form of systemic non-Langerhans cell histiocytosis with characteristic bone involvement. However, extraskeletal involvement occurs in approximately half of the patients. Because of its protean findings, the diagnosis of ECD is often delayed; thus, a clinical suspicion may prompt specific imaging studies to recognize suggestive signs of organ involvement. In this study, a case of a patient with ECD with...
Paper Details
Title
Erdheim-Chester Disease
Published Date
Aug 1, 2011
Journal
Volume
36
Issue
8
Pages
704 - 706
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