We describe a 76-year-old former smoker with a diagnosis of combined pulmonary fibrosis and emphysema associated with pulmonary hypertension and rapidly progressive right heart failure, in whom combined treatment with sitaxsentan and sildenafil resulted in sustained improvement of his clinical condition and exercise performance, without any relevant adverse events. Combined pulmonary fibrosis and emphysema comprises a recently identified syndrome, probably related to tobacco use, and characterized by the coexistence of upper-lobe emphysema and fibrotic changes of the lower lobes, preserved lung volumes, significant hypoxemia, and a high prevalence of pulmonary hypertension, resulting in severe dyspnea. To date, no prospective series, to the...
Pulmonary hypertension (PH) is present in an important proportion of patients with interstitial lung...
In 2005, the combined pulmonary fibrosis and emphysema (CPFE) was first defined as a distinct entity...
In 2015, the international guidelines for diagnosis and treatment of pulmonary hypertension (PH) wer...
We describe a 76-year-old former smoker with a diagnosis of combined pulmonary fibrosis and emphysem...
SummaryIntroductionSmoking can cause a variety of pulmonary interstitial diseases. Pulmonary fibrosi...
This study aims to describe the haemodynamic and survival characteristics of patients with pulmonary...
International audienceThe syndrome resulting from combined pulmonary fibrosis and emphysema has not ...
ABSTRACT: The syndrome resulting from combined pulmonary fibrosis and emphysema has not been compreh...
A syndrome associating an upper-lobe emphysema and pulmonary fibrosis of the lower lung was recently...
Combined pulmonary fibrosis and emphysema (CPFE) is a recently defined syndrome, in which centrilobu...
Introduction: Pulmonary fibrosis is a disease that is characterized by an accumulation of excess fi...
A 75-year-old woman with a history of smoking was admitted to the hospital with dyspnea and desatura...
Combined pulmonary fibrosis and emphysema (CPFE) has been increasingly recognized in the literature....
Background: The presence of emphysema is relatively common in patients with fibrotic interstitial lu...
Pulmonary hypertension (PH) is present in an important proportion of patients with interstitial lung...
Pulmonary hypertension (PH) is present in an important proportion of patients with interstitial lung...
In 2005, the combined pulmonary fibrosis and emphysema (CPFE) was first defined as a distinct entity...
In 2015, the international guidelines for diagnosis and treatment of pulmonary hypertension (PH) wer...
We describe a 76-year-old former smoker with a diagnosis of combined pulmonary fibrosis and emphysem...
SummaryIntroductionSmoking can cause a variety of pulmonary interstitial diseases. Pulmonary fibrosi...
This study aims to describe the haemodynamic and survival characteristics of patients with pulmonary...
International audienceThe syndrome resulting from combined pulmonary fibrosis and emphysema has not ...
ABSTRACT: The syndrome resulting from combined pulmonary fibrosis and emphysema has not been compreh...
A syndrome associating an upper-lobe emphysema and pulmonary fibrosis of the lower lung was recently...
Combined pulmonary fibrosis and emphysema (CPFE) is a recently defined syndrome, in which centrilobu...
Introduction: Pulmonary fibrosis is a disease that is characterized by an accumulation of excess fi...
A 75-year-old woman with a history of smoking was admitted to the hospital with dyspnea and desatura...
Combined pulmonary fibrosis and emphysema (CPFE) has been increasingly recognized in the literature....
Background: The presence of emphysema is relatively common in patients with fibrotic interstitial lu...
Pulmonary hypertension (PH) is present in an important proportion of patients with interstitial lung...
Pulmonary hypertension (PH) is present in an important proportion of patients with interstitial lung...
In 2005, the combined pulmonary fibrosis and emphysema (CPFE) was first defined as a distinct entity...
In 2015, the international guidelines for diagnosis and treatment of pulmonary hypertension (PH) wer...