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Usual interstitial pneumonia: typical, possible, and “inconsistent” patterns
Idiopathic pulmonary fibrosis is a severe and progressive chronic fibrosing interstitial lung disease, a definitive diagnosis being established by specific combinations of clinical, radiological, and pathological findings. According to current international guidelines, HRCT plays a key role in estab...
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| Publicat a: | J Bras Pneumol |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Sociedade Brasileira de Pneumologia e Tisiologia
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5790657/ https://ncbi.nlm.nih.gov/pubmed/29160385 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/S1806-37562016000000368 |
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