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CT findings in pulmonary alveolar proteinosis: serial changes and prognostic implications
BACKGROUND: Pulmonary alveolar proteinosis (PAP) is a rare disease of unknown origin, characterized by impaired surfactant metabolism. In some patients, residual disease is observed after treatment; notably, this may progress to end-stage pulmonary fibrosis. This study was performed to evaluate chan...
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| Pubblicato in: | J Thorac Dis |
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| Autori principali: | , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
AME Publishing Company
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6236152/ https://ncbi.nlm.nih.gov/pubmed/30505485 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/jtd.2018.09.86 |
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