PedAM
Pediatric Disease Annotations & Medicines
| Disease | pneumonia |
| Phenotype | C1800706|idiopathic pulmonary fibrosis |
| Sentences | 9 |
| PubMedID- 19597127 | idiopathic pulmonary fibrosis (ipf) (histopathology of usual interstitial pneumonia [uip]) is a progressive disease with poor prognosis. |
| PubMedID- 21166122 | These seven entities are idiopathic pulmonary fibrosis (with features typical of interstitial pneumonia), nonspecific interstitial pneumonia, cryptogenic organising pneumonia, respiratory bronchiolitis with interstitial lung disease, desquamative interstitial pneumonia, lymphocytic interstitial pneumonia, and acute idiopathic interstitial pneumonia (with features of diffuse alveolar damage). |
| PubMedID- 20855643 | The pathogenesis of chronic hypersensitivity pneumonitis in common with idiopathic pulmonary fibrosis: expression of apoptotic markers. |
| PubMedID- 25256743 | One cause of progressive pulmonary fibrosis is dysregulated wound healing after lung inflammation or damage in patients with idiopathic pulmonary fibrosis and severe acute respiratory distress syndrome. |
| PubMedID- 25389350 | Background: emphysema and fibrosis, typically the idiopathic pulmonary fibrosis (ipf) form of usual interstitial pneumonia (uip), can co-exist as combined pulmonary fibrosis emphysema (cpfe). |
| PubMedID- 24886550 | Background: the pathological appearance of idiopathic pleuroparenchymal fibroelastosis (ippfe) with hematoxylin-eosin staining is similar to that of usual interstitial pneumonia (uip) in patients with idiopathic pulmonary fibrosis (ipf). |
| PubMedID- 26578138 | idiopathic pulmonary fibrosis is a type of chronic fibrosing interstitial pneumonia, of unknown etiology, which is associated with a progressive decrease in pulmonary function and with high mortality rates. |
| PubMedID- 21415081 | (d) biopsy from another affected individual (iii.10) shows late stage idiopathic pulmonary fibrosis changes of bronchiolitis obliterans organising pneumonia and usual interstitial pneumonia. |
| PubMedID- 24836398 | Methods: we retrospectively compared the clinical data of ae-ipf-patients, idiopathic pulmonary fibrosis (ipf) with pneumonia-patients and slowly progressive ipf-patients. |
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