A Case of Incidentally-diagnosed Erdheim-Chester Disease

Erdheim-Chester disease (ECD) is a rare multisystemic non-Langerhans cell histiocytosis that may be clonal and inflammatory in origin. The hallmark of the disease is infiltration of various organ systems by CD68+/CD1a- histiocytes containing foamy lipid-laden inclusions. The manifestations and cours...

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Detalles Bibliográficos
Autores principales: Dave, Atman A, Gutschow, Susan E, Walker, Christopher M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2016
Materias:
Radiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5063637/
https://www.ncbi.nlm.nih.gov/pubmed/27752407
http://dx.doi.org/10.7759/cureus.781

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5063637/
https://www.ncbi.nlm.nih.gov/pubmed/27752407
http://dx.doi.org/10.7759/cureus.781

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