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Langerhans cell histiocytosis in adults: Advances in pathophysiology and treatment
Langerhans cell histiocytosis (LCH) is a rare systemic disorder characterized by the accumulation of CD1a+/Langerin+ LCH cells and wide‐ranging organ involvement. Langerhans cell histiocytosis was formerly referred to as histiocytosis X, until it was renamed in 1987. Langerhans cell histiocytosis β...
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| Publicat a: | Cancer Sci |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
John Wiley and Sons Inc.
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6272080/ https://ncbi.nlm.nih.gov/pubmed/30281871 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cas.13817 |
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