MeSH 搜索器

Idiopathic Pulmonary Fibrosis

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.
推出的年份: 2009
副标题
树号: C08.381.483.652.500, C08.381.483.652.500.750.624
MeSH 单一 ID: D054990
进入的组:
  • Idiopathic Pulmonary Fibroses
  • Pulmonary Fibroses, Idiopathic
  • Idiopathic Fibrosing Alveolitis, Chronic Form
  • Fibrosing Alveolitis, Cryptogenic
  • Fibrocystic Pulmonary Dysplasia
  • Dysplasia, Fibrocystic Pulmonary
  • Fibrocystic Pulmonary Dysplasias
  • Pulmonary Dysplasia, Fibrocystic
  • Cryptogenic Fibrosing Alveolitis
  • Cryptogenic Fibrosing Alveolitides
  • Fibrosing Alveolitides, Cryptogenic
  • Pulmonary Fibrosis, Idiopathic
  • Usual Interstitial Pneumonia
  • Interstitial Pneumonia, Usual
  • Usual Interstitial Pneumonias
  • Interstitial Pneumonitis, Usual
  • Pneumonitides, Usual Interstitial
  • Pneumonitis, Usual Interstitial
  • Usual Interstitial Pneumonitides
  • Usual Interstitial Pneumonitis
  • Familial Idiopathic Pulmonary Fibrosis
  • Idiopathic Pulmonary Fibrosis, Familial
早前的内容:
  • Pulmonary Fibrosis (1964-2008)

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