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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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| Publicado no: | Medicine (Baltimore) |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wolters Kluwer Health
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4985366/ https://ncbi.nlm.nih.gov/pubmed/26512552 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000001365 |
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