Adult pulmonary Langerhans cell histiocytosis revealed by central diabetes insipidus: A case report and literature review

Langerhans cell histiocytosis (LCH) is a rare systemic and heterogeneous disease secondary to proliferation and diffuse infiltration of immature CD1a-positive dendritic cells, also known as Langerhans cells. LCH affects predominantly paediatric patients and is rarely diagnosed in adulthood. Despite...

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Detalles Bibliográficos
Autores principales: Lourenço, Jorge, Ferreira, Cristina, Marado, Daniela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7403809/
https://www.ncbi.nlm.nih.gov/pubmed/32765877
http://dx.doi.org/10.3892/mco.2020.2100

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7403809/
https://www.ncbi.nlm.nih.gov/pubmed/32765877
http://dx.doi.org/10.3892/mco.2020.2100

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