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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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| Pubblicato in: | Respir Med Case Rep |
|---|---|
| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Elsevier
2020
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7658490/ https://ncbi.nlm.nih.gov/pubmed/33209579 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.rmcr.2020.101280 |
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