Advanced interstitial lung fibrosis with emphysema and pulmonary hypertension with no evidence for interstitial lung disease on high resolution CT

The diagnosis of idiopathic pulmonary arterial hypertension (iPAH) is complex and, besides invasive hemodynamic evaluation, includes several diagnostic steps to exclude any underlying diseases. The role of a decreased diffusion capacity of the lung for carbon monoxide (DLCO) is a matter of discussio...

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Detalles Bibliográficos
Autores principales: Foris, Vasile, Brcic, Luka, Douschan, Philipp, Kovacs, Gabor, Stacher-Priehse, Elvira, Olschewski, Horst
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6614945/
https://www.ncbi.nlm.nih.gov/pubmed/30729872
http://dx.doi.org/10.1177/2045894019832214

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6614945/
https://www.ncbi.nlm.nih.gov/pubmed/30729872
http://dx.doi.org/10.1177/2045894019832214

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