Erdheim–Chester disease presenting with cutaneous involvement: a case report and literature review

Erdheim–Chester disease (ECD) is a rare, systemic, non-familial histiocytic disorder, first described by Jakob Erdheim and William Chester in 1930. Most patients have multiple sites of involvement at presentation. The most common site of involvement is the long bones of the axial skeleton, which is...

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Main Authors: Volpicelli, Elgida Radoncipi, Doyle, Leona, Annes, Justin P., Murray, Michael F., Jacobsen, Eric, Murphy, George F., Saavedra, Arturo P.
Format: Artigo
Jezik:Inglês
Izdano: 2010
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Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC3619727/
https://ncbi.nlm.nih.gov/pubmed/21143617
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1600-0560.2010.01650.x
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