Initial presentation of Pulmonary Langerhans cell histiocytosis as recurrent spontaneous pneumothoraces

Pulmonary Langerhans cell histiocytosis (PLCH) is a rare cystic lung disease. The natural history is often unpredictable making it difficult to diagnose. We report a 63-year-old male with dyspnoea, chronic cough and recurrent respiratory tract infections, who developed progressive multifocal cystic...

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Detalles Bibliográficos
Autores principales: Keane, Ruaidhri J., Subramaniam, Abirami, Varghese, Chithra, Jeffers, Michael, Donnelly, Seamas C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658490/
https://www.ncbi.nlm.nih.gov/pubmed/33209579
http://dx.doi.org/10.1016/j.rmcr.2020.101280

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658490/
https://www.ncbi.nlm.nih.gov/pubmed/33209579
http://dx.doi.org/10.1016/j.rmcr.2020.101280

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