Idiopathic pulmonary fibrosis, formerly known as cryptogenic fibrosing alveolitis, is a rare, progressive illness of the respiratory system characterized by the thickening and stiffening of the lung tissue surrounding the air sacs, associated with the formation of scar tissue. It is a type of chronic pulmonary fibrosis marked by a progressive and irreversible decline in lung function.
Facts
Classification
ICD-10 ChapterX: Diseases of the Respiratory System 1 Communicable or Non-communicable Transmission Route Causative Agent
Causative Agent (category)Idiopathic / Multifactorial 2 Connections
Sources
1. Wikipedia: ICD-10
WikipediaList of chapters, Chapter XQuote, List of chapters, Chapter X
Diseases of the respiratory system
2. Idiopathic Pulmonary Fibrosis (Wikipedia)
WikipediaBody text, cause statement
The cause is unknown, hence the term idiopathic.
lead paragraph
The cause is unknown, hence the term idiopathic.
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