eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | idiopathic pulmonary fibrosis |
| Comorbidity | C0034069|pulmonary fibrosis |
| Sentences | 8 |
| 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- 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- 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- 25729724 | Dilds include interstitial lung diseases (ild) with a known cause (pneumoconiosis, ild associated with connective tissue disease, hypersensitivity pneumonitis [hp]), sarcoidosis, and idiopathic interstitial pneumonia (iip) including bronchiolitis obliterans organizing pneumonia (boop), eosinophilic pneumonia, nonspecific interstitial pneumonia (nsip) and idiopathic pulmonary fibrosis, a form of usual interstitial pneumonia (uip) according to the statement of the american thoracic society and the european respiratory society [2]. |
| 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- 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- 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- 23086930 | Dysregulated amphiregulin (ar) expression and egr receptor (egfr) activation have been described in animal models of pulmonary fibrosis and in patients with idiopathic pulmonary fibrosis. |
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