Cardiovascular Involvement in Erdheim–Chester Disease: A Case Report and Review of the Literature

Erdheim–Chester disease (ECD) is a rare, multiorgan, non-Langerhans cell histiocytosis of uncertain origin, characterized by systemic xanthogranulomatous infiltration from CD68+CD1a- histiocytes. Skeletal involvement is present in up to 96% of cases with bilateral osteosclerosis of meta-diaphysis of...

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Detalles Bibliográficos
Autores principales: Nicolazzi, Maria Anna, Carnicelli, Annamaria, Fuorlo, Mariella, Favuzzi, Angela Maria Rita, Landolfi, Raffaele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2015
Materias:
3400
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4985366/
https://www.ncbi.nlm.nih.gov/pubmed/26512552
http://dx.doi.org/10.1097/MD.0000000000001365

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4985366/
https://www.ncbi.nlm.nih.gov/pubmed/26512552
http://dx.doi.org/10.1097/MD.0000000000001365

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