How I manage pulmonary Langerhans cell histiocytosis

Pulmonary Langerhans cell histiocytosis (PLCH) is a rare sporadic cystic lung disease of unknown aetiology that is characterised by the infiltration and destruction of the wall of distal bronchioles by CD1a(+) Langerhans-like cells. In adults, PLCH is frequently isolated and affects young smokers of...

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Detalles Bibliográficos
Autores principales: Lorillon, Gwenaël, Tazi, Abdellatif
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2017
Materias:
Frontiers in Clinical Practice
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9489169/
https://www.ncbi.nlm.nih.gov/pubmed/28877978
http://dx.doi.org/10.1183/16000617.0070-2017

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9489169/
https://www.ncbi.nlm.nih.gov/pubmed/28877978
http://dx.doi.org/10.1183/16000617.0070-2017

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