PedAM

Pediatric Disease Annotations & Medicines

Disease	lung disease
Phenotype	C0034069\|pulmonary fibrosis
Sentences	17
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.
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- 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- 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- 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- 20655294	pulmonary fibrosis is a type of interstitial lung disease that causes progressive scarring in lung tissues.
PubMedID- 26399999	Idiopathic pulmonary fibrosis (ipf), the prototype of interstitial lung diseases, has the worst prognosis and is the only interstitial lung disease for which approved pharmacological treatments are available.
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- 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- 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- 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- 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- 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- 23668427	Secondly, there are patients whose predominant symptom is cough but clearly have conditions which are a recognised illness, such as pulmonary fibrosis due to interstitial lung disease or non cystic fibrosis bronchiectasis.
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.

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