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Case of Erdheim–Chester presenting with xanthelasma-like eruption and osteolytic bone lesions: A case report
Erdheim–Chester disease is a rare multisystemic non-Langerhans cell histiocytosis presenting 95% with skeletal lesions. Erdheim–Chester disease is due to mutations in the RAS-MEK-ERK pathway where 50% are due to BRAF-V600E mutations. Typical histopathological, clinical, and radiologic features are n...
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| Publicado no: | SAGE Open Med Case Rep |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
SAGE Publications
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6503601/ https://ncbi.nlm.nih.gov/pubmed/31105942 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2050313X19845217 |
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