PedAM
Pediatric Disease Annotations & Medicines
| Disease | pulmonary fibrosis |
| Phenotype | C1800706|usual interstitial pneumonia |
| Sentences | 7 |
| 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- 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- 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- 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- 23741087 | [5] symptomatic pulmonary fibrosis with a usual interstitial pneumonia pattern on high resolution computerized tomography and histopathology was seen in our case 2 years after the influenza infection. |
| PubMedID- 23434037 | Histologic features of mpo-anca-positive pulmonary fibrosis were compatible with the usual interstitial pneumonia pattern in which alveolar hemorrhage and capillaritis were not observed. |
| 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. |
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