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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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Detalles Bibliográficos
Autores principales: Chinchilla, Evelyn Alarcon, Gourde, Marie-Pascale, Turcotte, Karine, Mathieu, Steve, Amin-Hashem, Mohamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503601/
https://www.ncbi.nlm.nih.gov/pubmed/31105942
http://dx.doi.org/10.1177/2050313X19845217

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