PedAM
Pediatric Disease Annotations & Medicines
| Disease | pulmonary fibrosis |
| Phenotype | C0024115|lung disease |
| Sentences | 17 |
| PubMedID- 24480138 | In interstitial lung diseases, the diagnosis of idiopathic pulmonary fibrosis is important where pathology and radiology show usual interstitial pneumonia (uip) pattern. |
| PubMedID- 25288308 | Analysis of ct 3d reconstruction and hounsfield units demonstrated lung disease consistent with restrictive pulmonary fibrosis with an interstitial infiltrate, absence of air trapping, and decrease in total lung volume in group iu as compared to groups uu and pres i. |
| PubMedID- 24250731 | Thoracic radiologic abnormalities occur in over 90% in patients with sarcoidosis at some stage of the disease, whilst 20% develop chronic lung disease leads to pulmonary fibrosis. |
| PubMedID- 26064696 | She had late sequelae of radiotherapy including mediastinal and left pulmonary fibrosis, with severe restrictive lung disease (figure 1). |
| PubMedID- 22450861 | She also had other late sequelae of radiotherapy including thyroid cancer, mediastinal fribrosis and left pulmonary fibrosis with severe restrictive lung disease and a newly diagnosed renal carcinoma. |
| PubMedID- 26552223 | [computed tomography in evaluating the development of different types of pulmonary fibrosis in patients with interstitial lung diseases]. |
| PubMedID- 24860860 | The main indications for ltx in the pediatric population are pulmonary cystic fibrosis, interstitial lung disease associated with pulmonary fibrosis, and congenital vascular disease (4,5). |
| PubMedID- 21050542 | Objectives: to evaluate an improved quantitative lung fibrosis score based on a computer-aided diagnosis (cad) system that classifies ct pixels with the visual semi-quantitative pulmonary fibrosis score in patients with scleroderma-related interstitial lung disease (ssc-ild). |
| PubMedID- 21071376 | Thoracic radiologic abnormalities are seen at some stage in approximately 90% of patients with sarcoidosis, and an estimated 20% develop chronic lung disease leading to pulmonary fibrosis. |
| PubMedID- 24082203 | [9] the diagnosis of systemic sclerosis requires either the presence of the major criterion (typical cutaneous sclerosis involving areas proximal to metacapophalangeal or metatersophalangeal joint) or two of the three minor criteria (sclerodactyly, digital pitting scar and pulmonary fibrosis not attributed to primary lung disease). |
| PubMedID- 22402440 | With regards to pulmonary diseases and models, several studies also have demonstrated that opn expression is increased in mouse models of pulmonary fibrosis and in patients with chronic lung diseases, such as idiopathic pulmonary fibrosis (pardo et al., 2005; prasse et al., 2009; schneider et al., 2010). |
| PubMedID- 22815821 | Our observations suggest that exposure to lps, or other common environmental exposures that activate innate immunity, could contribute to acceleration of, or acute exacerbations of fibrotic lung disease in patients with pulmonary fibrosis. |
| PubMedID- 20966039 | Previous studies have identified subclinical lung disease in family members of probands with familial pulmonary fibrosis, but the natural history of preclinical pulmonary fibrosis is uncertain. |
| PubMedID- 22191026 | Patients who met the following criteria were categorized as having fibrosis: the presence of diffuse parenchymal lung disease with significant pulmonary fibrosis on ct, defined as reticular opacities with peripheral and basal predominance, honeycombing, architectural distortion, and/or traction bronchiectasis or bronchiolectasis; focal ground-glass opacities and/or areas of alveolar condensation may be associated, but should not be prominent. |
| PubMedID- 23903809 | The diagnosis of idiopathic cfip was first based on tsct results: presence of a diffuse parenchymal lung disease with significant pulmonary fibrosis, defined as reticular opacities with peripheral and basal predominance, honeycombing, architectural distortion and/or traction bronchiectasis or bronchiolectasis.13 patients found to have other distinct diseases on the basis of clinical and/or radiographic findings, associated with the development of pulmonary fibrosis, such as connective tissue disease, drug-induced lung disease, pneumoconiosis, hypersensitivity pneumonitis, sarcoidosis, pulmonary histiocytosis and lymphangioleiomyomatosis, were excluded. |
| PubMedID- 26104973 | Recent data suggest that antireflux surgery may be more effective in preventing lung disease progression in patients with idiopathic pulmonary fibrosis or lung transplant recipients who have evidence of allograft dysfunction associated with the presence of excessive ger. |
| PubMedID- 22826322 | Interstitial lung disease (ild) with pulmonary fibrosis is an important manifestation in systemic sclerosis (ssc, scleroderma) where it portends a poor prognosis. |
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