Gamuts

Diffuse mixed airspace-interstitial lung disease

Idiopathic pulmonary fibrosis (IPF) is a rare, progressive illness of the respiratory system, characterized by the thickening and stiffening of lung tissue, associated with the formation of scar tissue. It is a type of chronic scarring lung disease characterized by a progressive and irreversible decline in lung function. [Source: Wikipedia ]

May Be Caused by
Amiodarone
Bleomycin
Bronchiolo-alveolar carcinoma
Busulfan
Chronic pulmonary hemorrhage
Cyclophosphamide
Cytomegalovirus pneumonia
Desquamative interstitial pneumonitis
Drug toxicity
Gold
Goodpasture syndrome
Hypersensitivity pneumonitis
Idiopathic pulmonary hemosiderosis
Methotrexate
Mitomycin
Mycoplasma pneumonia
Nonspecific interstitial pneumonitis
Poison toxicity
Pulmonary edema in heart failure or ARDS
Sarcoidosis
SARS
Strongyloides pneumonia
May Be Caused by
Amiodarone
Bleomycin
Bronchiolo-alveolar carcinoma
Busulfan
Chronic pulmonary hemorrhage
Cyclophosphamide
Cytomegalovirus pneumonia
Desquamative interstitial pneumonitis
Drug toxicity
Gold
Goodpasture syndrome
Hypersensitivity pneumonitis
Idiopathic pulmonary hemosiderosis
Methotrexate
Mitomycin
Mycoplasma pneumonia
Nonspecific interstitial pneumonitis
Poison toxicity
Pulmonary edema in heart failure or ARDS
Sarcoidosis
SARS
Strongyloides pneumonia


Copyright © 2025, Charles E. Kahn, Jr., MD, MS
ALL RIGHTS RESERVED
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