Disease | lung disease |
Phenotype | C0032285|pneumonias |
Sentences | 6 |
PubMedID- 25362773 | Idiopathic interstitial pneumonias represent approximately 30% of all interstitial lung diseases. |
PubMedID- 24368713 | The diffuse idiopathic interstitial pneumonias describe a spectrum of parenchymal lung diseases sharing clinical, physiological, radiological and pathological similarities, including varying degrees of fibrosis, inflammation and vascular injury.1 idiopathic pulmonary fibrosis (ipf) is associated with usual interstitial pneumonia (uip), poor survival and limited treatment options.2 interstitial lung disease (ild), most typically presenting as non-specific interstitial pneumonitis, is a leading cause of death in systemic sclerosis (ssc)3 and a prominent clinical feature of other connective tissue diseases (ctds), including idiopathic inflammatory myopathy (iim) and sjögren syndrome. |
PubMedID- 26236603 | Given the rise in reported cases of p. multocida community acquired pneumonias, specifically in patients with structural lung disease, consideration should be made to avoid the use of macrolide therapy, especially as monotherapy, in patients with regular exposure to domesticated animals [12]. |
PubMedID- 21309737 | Idiopathic interstitial pneumonias are a group of idiopathic interstitial lung diseases of which idiopathic pulmonary fibrosis (ipf) is the lesion of usual interstitial pneumonia. |
PubMedID- 21207733 | Idiopathic interstitial pneumonias represent a group of complex lung diseases among which the most frequent types are idiopathic pulmonary fibrosis (ipf), idiopathic non-specific interstitial pneumonia (idiopathic nsip), and cryptogenic organizing pneumonia (cop). |
PubMedID- 22997396 | Objective: the interstitial pneumonias are a group of heterogeneous nonneoplastic lung diseases that may be idiopathic or associated with an underlying abnormality. |
Page: 1