Idiopathic pulmonary fibrosis (Q42939): Difference between revisions

@@ description / pt-br / description / pt-br @@
+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.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1074069640
@@ Property / Canonical URI: https://id.who.int/icd/entity/1074069640 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:CB03.4
@@ Property / CURIE: CID11:CB03.4 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-CB03.4
@@ Property / Canary Token: dki-india-CB03.4 / rank @@
+Normal rank
@@ Property / Verification Status @@
+Concluído
@@ Property / Verification Status: Concluído / rank @@
+Normal rank
@@ Property / Knowledge Architect @@
+https://pauloleads.com.br/cases-publicos/
+Normal rank
@@ Property / Collection date @@
+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-13T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 13 August 2026 / rank @@
+Normal rank
@@ Property / Linked ICD 10 @@
+J84.1
@@ Property / Linked ICD 10: J84.1 / rank @@
+Normal rank

Latest 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
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.