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Erdheim-Chester disease associated with hydrocaiycosis and arthropathy

✍ Scribed by R. Brown; R. Den Van Berg; N. P. Hurst; P. W. Allen

Publisher
John Wiley and Sons
Year
1988
Tongue
English
Weight
205 KB
Volume
31
Category
Article
ISSN
0004-3591

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## Abstract ## Objective Erdheim‐Chester disease (ECD) is a rare form of non–Langerhans' cell histiocytosis (LCH) of unknown etiology, characterized by diffuse histiocyte infiltration of bones and soft tissue. The purpose of this study was to assess cell proliferation and expression of cytokines,

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