New insights in lymphangioleiomyomatosis and pulmonary Langerhans cell histiocytosis

Lymphangioleiomyomatosis (LAM) and pulmonary Langerhans cell histiocytosis (PLCH) are rare diseases that lead to progressive cystic destruction of the lungs. Despite their distinctive characteristics, these diseases share several features. Patients affected by LAM or PLCH have similar radiological c...

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Detalles Bibliográficos
Autores principales: Torre, Olga, Elia, Davide, Caminati, Antonella, Harari, Sergio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2017
Materias:
Reviews
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9488980/
https://www.ncbi.nlm.nih.gov/pubmed/28954765
http://dx.doi.org/10.1183/16000617.0042-2017

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9488980/
https://www.ncbi.nlm.nih.gov/pubmed/28954765
http://dx.doi.org/10.1183/16000617.0042-2017

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