PedAM
Pediatric Disease Annotations & Medicines
| Disease | pneumonia |
| Phenotype | C0034069|pulmonary fibrosis |
| Sentences | 24 |
| PubMedID- 22096546 | Interstitial lung disease (ild), in particular interstitial pneumonia associated with pulmonary fibrosis, is a devastating chronic lung condition with poor prognosis. |
| 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- 19597127 | Idiopathic pulmonary fibrosis (ipf) (histopathology of usual interstitial pneumonia [uip]) is a progressive disease with poor prognosis. |
| PubMedID- 26278692 | Comparison of clinical characteristics and outcomes between combined pulmonary fibrosis and emphysema associated with usual interstitial pneumonia pattern and non-usual interstitial pneumonia. |
| PubMedID- 20882179 | By distinction to drug-induced pulmonary pneumonitis that may lead to pulmonary fibrosis, ncpe can be reversed upon prompt recognition, following immediate discontinuation of the offensive drug and start of intensive supportive treatment although fatalities have been reported. |
| PubMedID- 24970330 | Rac2 is involved in bleomycin-induced lung inflammation leading to pulmonary fibrosis. |
| 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. |
| 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- 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- 20836851 | Idiopathic pulmonary fibrosis (ipf) (histopathology of usual interstitial pneumonia, uip) is classified as one of the idiopathic interstitial pneumonias, representing an entity with unknown etiology, aggressive fibrogenesis and a very poor prognosis [1,2]. |
| PubMedID- 23020729 | In the context of clinical trials, pathologists are being asked to assign levels of confidence for histologic diagnosis of usual interstitial pneumonia in patients with idiopathic pulmonary fibrosis. |
| PubMedID- 24721403 | [il-17a promotes pulmonary inflammation in rats with pulmonary fibrosis induced by bleomycin]. |
| PubMedID- 22701025 | After extensive investigation, he was found to have pulmonary fibrosis with usual interstitial pneumonia pattern on high-resolution ct imaging and positive myeloperoxidase antineutrophil cytoplasmic antibodies (mpo-anca) with no infectious cause or other evidence of vasculitis organ involvement. |
| PubMedID- 25473539 | The autopsied lungs demonstrated a diffuse fibrotic nonspecific interstitial pneumonia (nsip) pattern with emphysema (combined pulmonary fibrosis and emphysema) and widespread severe intimal and medial thickening ranging from proximal elastic to distal muscular pulmonary arteries. |
| PubMedID- 21048214 | pulmonary fibrosis is associated with pulmonary inflammation, angiogenesis, and deposition of collagen and is modeled by instillation of bleomycin. |
| PubMedID- 20855643 | The pathogenesis of chronic hypersensitivity pneumonitis in common with idiopathic pulmonary fibrosis: expression of apoptotic markers. |
| PubMedID- 25889053 | Specifically, kk/hij, c57bl/6j, 129s1/svimj mice all had significant pulmonary fibrosis, with pneumonitis, when in distress and mice of the c3h/hej, a/j and akr/j strains succumbed with pneumonitis and no fibrosis. |
| 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- 20976305 | In chronic pulmonary fibrosis of viral pneumonia, mmp-2 (figure 3(f)) and mmp-9 (figure 3(g)) were expressed actively near the margin of intraluminal plugs of bronchioles as macrophage and mfbs. |
| PubMedID- 26266064 | Interstitial pneumonia with beginning pulmonary fibrosis was diagnosed in november 2011 during evaluation for progressive dyspnea. |
| 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- 22778574 | Chest ct revealed pulmonary fibrosis consistent with typical interstitial pneumonitis (uip pattern) showing reticular opacity at the subpleural area in both lungs, especially in the right lower lobe. |
| PubMedID- 22448329 | Imaging diagnosis of interstitial pneumonia with emphysema (combined pulmonary fibrosis and emphysema). |
| PubMedID- 20861649 | Background: chronic hypersensitivity pneumonitis (hp) can lead to irreversible pulmonary fibrosis. |
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