Multisystem Langerhans cell histiocytosis: Literature review and case report

Langerhans cell histiocytosis (LCH) refers to a group of diseases of unknown etiology, typically discovered in childhood, characterized by the accumulation of Langerhans cells (white blood cells with large cell nuclei that may contain cytoplasmic histiocytosis X bodies) involving one or more organ s...

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Detalles Bibliográficos
Autores principales: Cong, Cung-Van, Ly, Tran-Thi, Duc, Nguyen Minh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8891995/
https://www.ncbi.nlm.nih.gov/pubmed/35251425
http://dx.doi.org/10.1016/j.radcr.2022.02.024

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8891995/
https://www.ncbi.nlm.nih.gov/pubmed/35251425
http://dx.doi.org/10.1016/j.radcr.2022.02.024

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