Acute interstitial pneumonitis
Updates to Study Attributes
There is brogressionprogression of the bi-basilar traction broncheactasis and parenchymal architectural distortion of the lung bases.
Updates to Study Attributes
Persistent low lung volume with bi-basilar atelectasis/scaring/scarring.
Updates to Study Attributes
Persistent, essentially stable, bi-basilar traction broncheiactasis and architectural distortion.
Updates to Case Attributes
This case demonstrates the typical findings of AIPacute interstitial pneumonitis (AIP), considered as a rapidly progressive interstitial disease of unknown etiology.
The disease suspicion confirmed by open lung biopsy; which demonstrates the combination of diffuse alveolar damage (DAD) along with some changes of cryptogenic organizing pneumonia (COP).
-<p>This case demonstrates the typical findings of AIP, considered as a rapidly progressive interstitial disease of unknown etiology.</p><p>The disease suspicion confirmed by open lung biopsy; which demonstrates the combination of diffuse alveolar damage (DAD) along with some changes of cryptogenic organizing pneumonia (COP).</p>- +<p>This case demonstrates the typical findings of <a title="Acute interstitial pneumonitis" href="/articles/acute-interstitial-pneumonitis">acute interstitial pneumonitis</a> (AIP), considered a rapidly progressive interstitial disease of unknown etiology.</p><p>The disease suspicion confirmed by open lung biopsy; which demonstrates the combination of <a title="Diffuse alveolar damage" href="/articles/diffuse-alveolar-damage">diffuse alveolar damage</a> (DAD) along with some changes of <a title="Cryptogenic organizing pneumonia" href="/articles/cryptogenic-organising-pneumonia-1">cryptogenic organizing pneumonia</a> (COP).</p>