Cargando…
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...
Autores principales: | Lorillon, Gwenaël, Tazi, Abdellatif |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
European Respiratory Society
2017
|
Materias: | |
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 |
Ejemplares similares
-
Psychological features of adult patients with langerhans cell histiocytosis
por: Bugnet, Emmanuelle, et al.
Publicado: (2021) -
Clarifying the relationship between pulmonary langerhans cell histiocytosis and Alpha 1 antitrypsin deficiency
por: McCarthy, Cormac, et al.
Publicado: (2021) -
Management and outcomes of pneumothorax in adult patients with Langerhans cell Histiocytosis
por: Le Guen, Pierre, et al.
Publicado: (2019) -
Lack of evidence for the involvement of Merkel cell polyomavirus in pulmonary Langerhans cell histiocytosis
por: Jouenne, Fanélie, et al.
Publicado: (2020) -
Extrathoracic investigation in adult patients with isolated pulmonary langerhans cell histiocytosis
por: Tazi, Abdellatif, et al.
Publicado: (2016)