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| {{DX tag | Respiratory | | Interstitial Pneumonitis | INTERSTITIAL PNEUMONITIS | 2700 | No | 0 | | | | }}''Notes: '' | | {{DX tag | Respiratory | | Interstitial Pneumonitis | INTERSTITIAL PNEUMONITIS | 2700 | No | 0 | | | | }}''Notes: '' |
| Interstitial lung disease (ILD), or diffuse parenchymal lung disease (DPLD),[1] is a group of lung diseases affecting the interstitium (the tissue and space around the air sacs of the lungs).[2] It concerns alveolar epithelium, pulmonary capillary endothelium, basement membrane, perivascular and perilymphatic tissues. It may occur when an injury to the lungs triggers an abnormal healing response. Ordinarily, the body generates just the right amount of tissue to repair damage. But in interstitial lung disease, the repair process goes awry and the tissue around the air sacs (alveoli) becomes scarred and thickened. This makes it more difficult for oxygen to pass into the bloodstream. The term ILD is used to distinguish these diseases from obstructive airways disease
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| **https://en.wikipedia.org/wiki/Interstitial_lung_disease
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| ILD may be classified according to the cause.[5] One method of classification is as follows:
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| Inhaled substances
| | [https://en.wikipedia.org/wiki/Interstitial_lung_disease See wikipedia} |
| Inorganic
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| Silicosis
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| Asbestosis
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| Berylliosis
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| Organic
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| Hypersensitivity pneumonitis
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| Drug-induced
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| Antibiotics
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| Chemotherapeutic drugs
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| Antiarrhythmic agents
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| Statins
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| Connective tissue and Autoimmune diseases
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| Systemic sclerosis
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| Polymyositis
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| Dermatomyositis
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| Systemic lupus erythematosus
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| Rheumatoid arthritis
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| Infection
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| Atypical pneumonia
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| Pneumocystis pneumonia (PCP)
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| Tuberculosis
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| Chlamydia trachomatis
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| Respiratory Syncytial Virus
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| Idiopathic
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| Sarcoidosis
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| Idiopathic pulmonary fibrosis
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| Hamman-Rich syndrome
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| Antisynthetase syndrome
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| Malignancy
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| Lymphangitic carcinomatosis
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