PedAM
Pediatric Disease Annotations & Medicines
| Disease | pulmonary fibrosis |
| Phenotype | C0032285|pneumonia |
| Sentences | 11 |
| 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- 22448329 | Imaging diagnosis of interstitial pneumonia with emphysema (combined pulmonary fibrosis and emphysema). |
| 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- 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- 26266064 | Interstitial pneumonia with beginning pulmonary fibrosis was diagnosed in november 2011 during evaluation for progressive dyspnea. |
| PubMedID- 22096546 | Interstitial lung disease (ild), in particular interstitial pneumonia associated with pulmonary fibrosis, is a devastating chronic lung condition with poor prognosis. |
| PubMedID- 25378837 | According to 2013 update, there are three broad categories: first, major idiopathic interstitial pneumonias comprising of idiopathic pulmonary fibrosis (ipf), nonspecific interstitial pneumonia, rb-ild, desquamative interstitial pneumonia, cryptogenic organizing pneumonia and acute interstitial pneumonia. |
| PubMedID- 25591144 | However, acute respiratory distress syndrome, acute interstitial pneumonia, and acute exacerbation of idiopathic pulmonary fibrosis, which, unlike aep are mostly life-threatening diseases, also exhibit dad. |
| 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- 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- 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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