Erdheim-Chester Disease

Known as: Lipid Granulomatosis, Erdheim Chester Disease, Lipogranulomatosis 
A very rare, multisystem non-Langerhans cell histiocytosis that predominantly affects adults. It is characterized by the proliferation in the tissues… (More)
National Institutes of Health

Papers overview

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2015
2015
BACKGROUND The diagnosis of Erdheim-Chester disease, a rare illness, is difficult and requires increased awareness. CASE REPORT… (More)
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2012
2012
Introduction Erdheim-Chester disease (ECD) is a rare, non-Langerhans histiocytosis characterized by xanthogranulomatous… (More)
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2011
2011
BACKGROUND Erdheim-Chester disease (ECD) is a rare multisystem non-Langerhans cell histiocytosis that is characterized… (More)
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2010
2010
Erdheim-Chester disease is a rare non-Langerhans cell histiocytosis of unknown etiology, the commonest sites of involvement being… (More)
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Review
2006
Review
2006
A 42-year-old woman suffered from pain in both legs, and fever. She was diagnosed with Erdheim-Chester disease (ECD), based upon… (More)
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2005
2005
Erdheim-Chester disease is a disseminated non-Langerhans' cell histiocytosis involving multiple organs with characteristic… (More)
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2004
2004
We describe a rare case of non-Langerhans histiocytosis, consistent with Erdheim-Chester disease (ECD), which presented with… (More)
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2004
2004
Pituitary morphologic changes in patients with Erdheim-Chester disease have not been described in detail. We report here the… (More)
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2000
2000
We report on a rare manifestation of Erdheim-Chester disease with intramuscular lipogranuloma. The patient was a 66-year-old man… (More)
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1997
1997
A 33-year-old woman presented with a 3-year history of progressive numbness in the hand, cerebellar ataxia, limb weakness… (More)
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