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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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Dades bibliogràfiques
Publicat a:Respirol Case Rep
Autors principals: Divithotawela, Chandima, Apte, Simon H., Tan, Maxine E., De Silva, Tharushi A., Chambers, Daniel C.
Format: Artigo
Idioma:Inglês
Publicat: John Wiley & Sons, Ltd 2020
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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