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Pulmonary alveolar proteinosis after lung transplantation
We report the case of a 69‐year‐old man five‐month post double lung transplant for idiopathic pulmonary fibrosis (IPF) who presented with progressive breathlessness, loss of lung function, and diffuse ground glass shadowing on the chest computed tomography. Transbronchial lung biopsy revealed foamy...
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| Publicat a: | Respirol Case Rep |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
John Wiley & Sons, Ltd
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7199162/ https://ncbi.nlm.nih.gov/pubmed/32377344 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/rcr2.566 |
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