Idiopathic pulmonary fibrosis (Q42939): Difference between revisions
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Fibrose pulmonar idiopática (FPI) é definida como uma forma específica de pneumonia (pneumonite) intersticial crônica progressiva de causa desconhecida, que ocorre principalmente em adultos mais velhos, limitada aos pulmões e associada a padrão histopatológico e/ou radiológico de PIU (pneumonia intersticial usual). A definição de FPI requer a exclusão de outras formas de pneumonia (pneumonite) intersticial, incluindo outras pneumonias (pneumonites) intersticiais idiopáticas e Doença Intersticial Pulmonar (DIP) associada a exposição ambiental, medicação ou doença sistêmica. | |||
| description / en | description / en | ||
Idiopathic pulmonary fibrosis (IPF) is defined as a specific form of chronic, progressive fibrosing interstitial pneumonia (pneumonitis) of unknown cause, occurring primarily in older adults, limited to the lungs, and associated with the histopathologic and/or radiologic pattern of UIP (Usual Interstitial Pneumonia). The definition of IPF requires the exclusion of other forms of interstitial pneumonia (pneumonitis) including other idiopathic interstitial pneumonias (pneumonitis) and Interstitial Lung Disease (ILD) associated with environmental exposure, medication, or systemic disease. | |||
Revision as of 09:42, 13 August 2026
Idiopathic pulmonary fibrosis (IPF) is defined as a specific form of chronic, progressive fibrosing interstitial pneumonia (pneumonitis) of unknown cause, occurring primarily in older adults, limited to the lungs, and associated with the histopathologic and/or radiologic pattern of UIP (Usual Interstitial Pneumonia). The definition of IPF requires the exclusion of other forms of interstitial pneumonia (pneumonitis) including other idiopathic interstitial pneumonias (pneumonitis) and Interstitial Lung Disease (ILD) associated with environmental exposure, medication, or systemic disease.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | CB03.4 |
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| English | Idiopathic pulmonary fibrosis |
Idiopathic pulmonary fibrosis (IPF) is defined as a specific form of chronic, progressive fibrosing interstitial pneumonia (pneumonitis) of unknown cause, occurring primarily in older adults, limited to the lungs, and associated with the histopathologic and/or radiologic pattern of UIP (Usual Interstitial Pneumonia). The definition of IPF requires the exclusion of other forms of interstitial pneumonia (pneumonitis) including other idiopathic interstitial pneumonias (pneumonitis) and Interstitial Lung Disease (ILD) associated with environmental exposure, medication, or systemic disease. |
