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Respiratory Tract Diseases > Lung Diseases > Lung Diseases, Interstitial > Pulmonary Fibrosis > Idiopathic Pulmonary Fibrosis
Pathological Conditions, Signs and Symptoms > Pathologic Processes > Fibrosis > Pulmonary Fibrosis > Idiopathic Pulmonary Fibrosis

Término preferido

Idiopathic Pulmonary Fibrosis  

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Tipo

  • mesh:Descriptor

Definición

  • A common interstitial lung disease of unknown etiology, usually occurring between 50-70 years of age. Clinically, it is characterized by an insidious onset of breathlessness with exertion and a nonproductive cough, leading to progressive DYSPNEA. Pathological features show scant interstitial inflammation, patchy collagen fibrosis, prominent fibroblast proliferation foci, and microscopic honeycomb change.

Concepto genérico

Conceptos específicos

Etiquetas alternativas

  • Cryptogenic Fibrosing Alveolitis
  • Fibrocystic Pulmonary Dysplasia
  • Fibrosing Alveolitis, Cryptogenic
  • Idiopathic Fibrosing Alveolitis, Chronic Form
  • Pulmonary Fibrosis, Idiopathic

En otras lenguas

  • Fibrose pulmonaire idiopathique

    francés

  • Alvéolite fibrosante cryptogénique
  • Fibrose interstitielle diffuse idiopathique
  • FPI (Fibrose Pulmonaire Idiopathique)
  • Pneumonie interstitielle usuelle

URI

http://data.loterre.fr/ark:/67375/JVR-PRFK0DWR-M

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RDF/XML TURTLE JSON-LD Creado 8/7/08, última modificación 28/4/22