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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...
Autores principales: | Nicolazzi, Maria Anna, Carnicelli, Annamaria, Fuorlo, Mariella, Favuzzi, Angela Maria Rita, Landolfi, Raffaele |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2015
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Materias: | |
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 |
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