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radiologyassistant ild nonspecificinterstitialpneumonia nsip chronic cxr ggo groundglass hypersensitivitypneumonitis pulmonary reticular usual usualinterstitialpneumonitis acuteinterstitialpneumonia aip comparison cystic differential druginduced drugrelated
Ground-glass opacity Ground-glass opacity (GGO) represents: - Filling of the alveolar spaces with pus, edema, hemorrhage, inflammation or
predominance: UIP ... Hypersensitivity pneumonitis ... bronchiolitis #Diagnosis ... #Radiology #Pulmonary ... #CTChest #GGO #
The idiopathic interstitial pneumonias (IIPs) comprise a heterogenous group of disorders. They represent fundamental responses of
pneumonias (IIPs ... indicates unknown cause ... combinations of fibrosis ... #Diagnosis #Radiology ... #Pulmonary #CTChest
HRCT findings in UIP Honeycombing consisting of multilayered thick-walled cysts. Architectural distortion with traction bronchiectasis due to fibrosis. Predominance
bronchiectasis due to fibrosis ... lymphadenopathy #Clinical ... #Radiology #CTChest ... #Usual #Interstitial ... #Pneumonitis #ILD
On the left a chest film of a patient with UIP due to IPF. The findings on
volume loss and fibrotic ... reticular densities caused ... #Clinical #Radiology ... #CXR #CTChest # ... #Usual #Interstitial
UIP with honeycombing (left) and chronic HP (right) Differential diagnosis of Hypersensitivity Pneumonitis. Subacute stage: - RB-ILD: seen in
) Differential diagnosis ... Hypersensitivity Pneumonitis ... In chronic HP fibrotic ... #Clinical #Diagnosis ... #Radiology #CTChest
UIP UIP is a histologic pattern of pulmonary fibrosis. On a chest X-ray UIP manifests as a reticular
pattern of pulmonary fibrosis ... On a chest X-ray ... to confirm the diagnosis ... #Clinical #Radiology ... #Interstitial #
On the left a patient who is treated with cytotoxic drugs for a hematologic malignancy. The radiographic
and non-specific interstitial ... pneumonitis or ... patients with a UIP ... #Clinical #Radiology ... #CTChest #DrugInduced
Acute interstitial pneumonia (AIP, earlier named Hamman Rich Pneumonitis) is a rare idiopathic lung disease characterized
Acute interstitial ... named Hamman Rich Pneumonitis ... with subsequent fibrosis ... #Clinical #Radiology ... #CTChest #AIP #
On the left a patient with GGO as dominant pattern. In addition there is traction bronchiectasis indicating
This case is one ... As in UIP (usual ... from that seen in UIP ... #Clinical #Radiology ... #CTChest #NSIP
Chronic hypersensitivity pneumonitis (2) The case on the left shows an inspiratory and expiratory scan: the mosaic
(2) The case on ... Signs of fibrosis ... left suggest the diagnosis ... #Clinical #Radiology ... #CTChest #Chronic
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