Abstract
BackgroundErdheim-Chester disease (ECD) is a rare, inflammatory disease of unknown etiology, characterized by xanthogranulomatous infiltration of tissues by foamy, CD 68+, CD1a-, S-100- macrophages [1]. ECD almost invariably involves long...
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
