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Bosentan for pulmonary hypertension secondary to idiopathic pulmonary fibrosis
Pulmonary hypertension is a poor prognostic factor in patients with interstitial lung disease. No established treatment exists for pulmonary hypertension secondary to interstitial pneumonia. We describe the case of an 81-year-old woman with idiopathic pulmonary fibrosis (IPF), who was admitted to ou...
Salvato in:
Pubblicato in: | Respir Med Case Rep |
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Autori principali: | , , , |
Natura: | Artigo |
Lingua: | Inglês |
Pubblicazione: |
Elsevier
2014
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Soggetti: | |
Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4356039/ https://ncbi.nlm.nih.gov/pubmed/26029570 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.rmcr.2014.11.008 |
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