Interstitial Lung Disease |
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Conditions and Treatments
The UCSF Interstitial Lung Disease Program evaluates all forms of interstitial lung disease (ILD). The following is a list of some of these conditions:
- Acute Eosinophilic Pneumonia
- Acute Interstitial Pneumonia (AIP or Hamman-Rich Syndrome)
- Asbestosis
- Bronchiolitis
- Chronic Eosinophilic Pneumonia
- Connective Tissue-related ILD
- Myositis-related ILD
- Rheumatoid arthritis-related ILD
- Scleroderma-related ILD
- Sjogren's syndrome-related ILD
- Systemic Lupus Erythematosis-related ILD
- Undifferentiated Connective Tissue Disease-related ILD
- Cryptogenic Organizing Pneumonia (COP)
- Desquamative Interstitial Pneumonia (DIP)
- Diffuse Alveolar Hemorrhage (DAH)
- Drug-related ILD
- Hypersensitivity Pneumonitis
- Idiopathic Pulmonary Fibrosis (IPF)
- Langerhan's Cell Histiocytosis (aka Eosinophilic granuloma or Histiocytosis X)
- Lymphangioleiomyomatosis (LAM)
- Lymphocytic interstitial Pneumonia (LIP)
- Non-specific Interstitial Pneumonia (NSIP)
- Pulmonary Alveolar Proteinosis (PAP)
- Radiation fibrosis
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- Respiratory Bronchiolitis-related ILD (RB-ILD)
- Sarcoidosis
- Wegener's granulomatosis and other vasculitidies
Reviewed by health care specialists at UCSF Medical Center. Last updated September 16, 2008
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