Idiopathic interstitial pneumonia
Idiopathic Interstitial Pneumonia Microchapters |
Differentiating Idiopathic interstitial pneumonia from other Diseases |
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Diagnosis |
Treatment |
Case Studies |
Idiopathic interstitial pneumonia On the Web |
American Roentgen Ray Society Images of Idiopathic interstitial pneumonia |
Directions to Hospitals Treating Idiopathic interstitial pneumonia |
Risk calculators and risk factors for Idiopathic interstitial pneumonia |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ahmed Zaghw, M.D. [2] Template:CL
Overview
Historical Perspective
Classification
Pathophysiology
Causes
Differentiating Idiopathic interstitial pneumonia from other Diseases
Epidemiology and Demographics
The true incidence is unknown. UIP is the most common (50%-60%) of the idiopathic interstitial pneumonia, then NSIP 14%-36%, then DIP/RB-ILD (10%-17%) and AIP (0%-2%)[1]
Natural History, Complications and Prognosis
Diagnosis
History and Symptoms | Physical Examination | Laboratory Findings |CT | Other Imaging Findings | Other Diagnostic Studies
Treatment
Medical Therapy | Surgery | Primary Prevention | Secondary Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies