GERD and idiopathic pulmonary fibrosis: cause or effect
نویسندگان
چکیده
منابع مشابه
Pediatric Idiopathic Pulmonary Fibrosis: A Case Series report
Khalilzadeh S1, Baghaei N2, Bolorsaz MR1, Masjedi MR3 1. Associate professor, Department of pediatrics, Education, research and treatment center of tuberculosis and long diseases, Shahid Beheshti University of medical sciences 2. Assistant professor, Department of pediatrics, Education, research and treatment center of tuberculosis and long diseases, Shahid Beheshti University of medical s...
متن کاملREPORT OF FOUR CASES OF FAMILIAL IDIOPATHIC PULMONARY FIBROSIS
A 25 year old male and his 46 year old aunt presented with shortness of breath and a dramatic response to steroids. The other two patients are sisters with more advanced disease. One of these responded partially to steroids, while the other died within 4 months of treatment. The genetic basis and pathogenesis are discussed.
متن کاملThe Cause of Idiopathic Pulmonary Fibrosis: A Hypothesis
Idiopathic pulmonary fibrosis (IPF) is a rapidly fatal condition of unknown cause. The alveolar membrane becomes thickened with collagen and inflammatory and immune cells, which accumulate in the sub-alveolar tissues. The reduction in the ability of oxygen to diffuse across the membrane leads inevitably to progressive anoxia. There is no satisfactory treatment. It is proposed that the histologi...
متن کاملPulmonary Rehabilitation in Idiopathic Pulmonary Fibrosis: A Chance for a Multidisciplinary Treatment Approach
Background and Objectives: Idiopathic pulmonary fibrosis (IPF) is characterized by progressively worsening lung function, ventilation capacity, dyspnea, and finally reduced exercise intolerance. All of these have a significant negative impact on functional capacity and quality of life. In this study, we aim to evaluate the effects of pulmonary rehabilitation (PR) in IPF and assess the predictor...
متن کامل[Idiopathic Pulmonary Fibrosis].
Idiopathic pulmonary fibrosis (IPF) is the most common idiopathic interstitial pneumonia and a disease of the elderly. Cigarette smoking and longterm exposure to substances harming alveolar epithelial cells are risk factors for the development of IPF. There is also evidence for a genetic susceptibility. IPF is defined as the idiopathic variant of Usual Interstitial Pneumonitis (UIP). Diagnosis ...
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ژورنال
عنوان ژورنال: Current Respiratory Care Reports
سال: 2013
ISSN: 2161-332X
DOI: 10.1007/s13665-013-0066-9