Idiopathic pulmonary fibrosis
Idiopathic pulmonary fibrosis | |
Extensive lung fibrosis from usual interstitial pneumonitis | |
ICD-9 | 516.3 |
OMIM | 178500 |
DiseasesDB | 4815 |
MedlinePlus | 000069 |
MeSH | D011658 |
Idiopathic pulmonary fibrosis Microchapters |
Differentiating Idiopathic pulmonary fibrosis from other Diseases |
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Diagnosis |
Treatment |
Case Studies |
Idiopathic pulmonary fibrosis On the Web |
American Roentgen Ray Society Images of Idiopathic pulmonary fibrosis |
Directions to Hospitals Treating Idiopathic pulmonary fibrosis |
Risk calculators and risk factors for Idiopathic pulmonary fibrosis |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: Cryptogenic fibrosing alveolitis; IPF
Overview
Historical Perspective
Classification
Pathophysiology
Causes
Differentiating Idiopathic pulmonary fibrosis from other Diseases
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications and Prognosis
Diagnosis
Diagnostic Criteria | History and Symptoms | Physical Examination | Laboratory Findings | Electrocardiogram | Chest X Ray | CT | Echocardiography or Ultrasound | Other Imaging Findings | Other Diagnostic Studies
Treatment
Medical Therapy | Surgery | Primary Prevention | Secondary Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies
Case Studies
de:Idiopathische interstitielle Pneumonie#Idiopathische_pulmonale_Fibrose_.28IPF.29
fi:Idiopaattinen keuhkofibroosi