Interstitial pneumonitis
Interstitial Pneumonitis | |
---|---|
[[File:|250px|]] | |
Synonyms | |
Pronounce | |
Specialty | Pulmonology |
Symptoms | Shortness of breath, dry cough, fatigue |
Complications | Respiratory failure, Pulmonary hypertension |
Onset | |
Duration | |
Types | Acute, chronic |
Causes | Infection, Autoimmune diseases, exposure to toxins |
Risks | Smoking, genetics, certain medications |
Diagnosis | Chest X-ray, CT scan, Lung biopsy |
Differential diagnosis | Pneumonia, Pulmonary edema, Lung cancer |
Prevention | Avoidance of known toxins, smoking cessation |
Treatment | Corticosteroids, Immunosuppressive drugs, oxygen therapy |
Medication | |
Prognosis | Varies |
Frequency | |
Deaths |
Interstitial pneumonitis is a form of pneumonia characterized by inflammation of the interstitial tissue of the lung, leading to severe scarring (fibrosis). This condition is part of a larger group of diseases known as interstitial lung diseases, which affect the tissue and space around the air sacs of the lungs.
Causes[edit | edit source]
Interstitial pneumonitis can be caused by a variety of factors, including:
- Infections by viruses, bacteria, or fungi
- Autoimmune diseases such as rheumatoid arthritis, scleroderma, or systemic lupus erythematosus
- Exposure to environmental and occupational irritants such as asbestos, silica, or coal dust
- Radiation therapy to the chest
- Use of certain medications, including chemotherapy drugs and heart arrhythmia medications
Symptoms[edit | edit source]
Common symptoms of interstitial pneumonitis include:
- Persistent dry cough
- Shortness of breath, especially during or after physical activity
- Fatigue and weakness
- Unintended weight loss
- Chest discomfort
Diagnosis[edit | edit source]
Diagnosis of interstitial pneumonitis involves a combination of clinical evaluation, imaging, and sometimes invasive procedures such as a lung biopsy. Key diagnostic tools include:
- Chest X-rays
- High-resolution CT scans
- Pulmonary function tests
- Bronchoscopy with or without biopsy
Treatment[edit | edit source]
Treatment for interstitial pneumonitis focuses on reducing inflammation and preventing further lung damage. Common treatments include:
- Corticosteroids to reduce inflammation
- Immunosuppressive drugs to control the immune system
- Oxygen therapy to manage symptoms of low blood oxygen levels
- Pulmonary rehabilitation to improve lung function and quality of life
In severe cases, a lung transplant may be considered.
Prognosis[edit | edit source]
The prognosis for interstitial pneumonitis varies widely depending on the underlying cause, the severity of the disease at diagnosis, and the patient's overall health. Early diagnosis and treatment are crucial for improving outcomes.
See also[edit | edit source]
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Contributors: Prab R. Tumpati, MD