Disease | pneumonia |
Phenotype | C2350236|idiopathic interstitial pneumonias |
Sentences | 14 |
PubMedID- 24578677 | Idiopathic ppfe has been listed as one of the rare idiopathic interstitial pneumonias (iips) in the revised international multidisciplinary classification of the iips [2]. |
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- 20502709 | We have previously reported that ∼25% of human subjects with the sporadic idiopathic interstitial pneumonias have short telomere lengths (<10th percentile) in the absence of telomerase mutations[19], suggesting a role of this epigenetic modification in the development of non-familial pulmonary fibrosis. |
PubMedID- 26557259 | Ipf is the most common of the idiopathic interstitial pneumonias and is a chronic fibrotic, irreversibly progressive ild with an estimated incidence in the nordic countries of 0.4–10/100,000 corresponding to 1–980 new ipf patients each year in iceland and sweden, respectively. |
PubMedID- 23984154 | Though the ats/ers consensus classification on idiopathic interstitial pneumonias suggest that a diagnosis of cop may be confirmed by transbronchial biopsy in the appropriate clinical setting, many experts believe that a surgical lung biopsy is needed for confirmation as such pathological changes can occur around vasculitis, eosinophilic pneumonia, nonspecific interstitial pneumonia, hypersensitivity pneumonitis, and malignancy [1, 4]. |
PubMedID- 23316404 | The idiopathic interstitial pneumonias (iip) is defined as a group of chronic, progressive diffuse parenchymal lung diseases with unclear cause, characterized by expansion of the interstitial compartment of inflammatory cells, and is potential to develop pulmonary fibrosis in many cases. |
PubMedID- 26029526 | The recent published updated classification of idiopathic interstitial pneumonias (iip) classifies ippfe in the group of rare iip [4]. |
PubMedID- 23734820 | Idiopathic interstitial pneumonias (iips) make up a heterogeneous group of diseases, which are collectively included in the umbrella term “interstitial lung diseases (ilds)” [1]. |
PubMedID- 22205929 | These results implicate for the first time the hsv-1 with fibrotic idiopathic interstitial pneumonias since the virus presented similar incidence in two different biological samples. |
PubMedID- 26013144 | It is the most common of the idiopathic interstitial pneumonias, is increasing in prevalence, and it is a progressive disease that causes significant morbidity and mortality. |
PubMedID- 25378843 | [45] with subsequent characterization of idiopathic interstitial pneumonias (iips),[16] an increase in the burden of ipf is being reported from various centers in india. |
PubMedID- 26202767 | Ct images of 74 patients with fibrotic idiopathic interstitial pneumonias (ipf, 36; non-specific interstitial pneumonia, 9; unclassifiable idiopathic interstitial pneumonia, 29) were analyzed via in-house computer software, which automatically calculated haa%, ca%, mean lung density (mld), standard deviation of lung density (sd-ld), kurtosis, and skewness from ct attenuation histograms. |
PubMedID- 26415510 | Human lung biopsies of patients with idiopathic interstitial pneumonias (iip), ipf and nsip, and human control lung tissue samples, were obtained in accordance to an approved protocol by the institutional ethics committees of the university hospitals geneva (hug) and the hôpital bichat, paris. |
PubMedID- 24270907 | Theoretically, idiopathic interstitial pneumonias could be caused by theepstein-barr virus, cytomegalovirus, adenovirus, hepatitis c virus, respiratorysyncytial virus, and herpesvirus, which may be present in such small amounts or suchconfiguration that routine histopathological analysis or viral culture techniquescannot detect them. |
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