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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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| Autores principales: | , , , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2010
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| Materias: | |
| Acceso en línea: | 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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