9 results
Ground-glass opacity
Ground-glass opacity (GGO) represents:
- Filling of the alveolar spaces with pus, edema, hemorrhage, inflammation or
predominance: UIP ... , NSIP, DIP. - Centrilobular ... bronchiolitis #Diagnosis #Radiology ... #Pulmonary #CTChest ... #RadiologyAssistant
HRCT findings in UIP
Honeycombing consisting of multilayered thick-walled cysts.
Architectural distortion with traction bronchiectasis due to fibrosis.
Predominance
lymphadenopathy #Clinical ... #Radiology #CTChest ... #Usual #Interstitial ... #Pneumonitis #ILD ... #RadiologyAssistant
The idiopathic interstitial pneumonias (IIPs) comprise a heterogenous group of disorders. 
They represent fundamental responses of
pneumonias (IIPs ... combinations of fibrosis ... arthritis findings of NSIP ... #Diagnosis #Radiology ... #Pulmonary #CTChest
UIP with honeycombing (left) and chronic HP (right)
Differential diagnosis of Hypersensitivity Pneumonitis.
Subacute stage:
- RB-ILD: seen in
chronic HP (right) Differential ... Hypersensitivity Pneumonitis ... #Clinical #Diagnosis ... #Radiology #CTChest ... #Mimic #ILD #RadiologyAssistant
The predominant finding is ground glass opacity (GGO).
There is very subtle traction bronchiectasis, indicating that the
the result of fibrosis ... distribution of UIP ... #Clinical #Radiology ... #CTChest #NSIP ... #RadiologyAssistant
The predominant finding is ground glass opacity (GGO).
There is very subtle traction bronchiectasis, indicating that the
the result of fibrosis ... distribution of UIP ... #Clinical #Radiology ... #CTChest #NSIP ... #RadiologyAssistant
On the left a chest film of a patient with UIP due to IPF.
The findings on
volume loss and fibrotic ... #Clinical #Radiology ... #CXR #CTChest # ... #Usual #Interstitial ... #ILD #RadiologyAssistant
On the left a patient who is treated with cytotoxic drugs for a hematologic malignancy.
The radiographic
patients with a UIP ... pattern or NSIP ... #Clinical #Radiology ... #CTChest #DrugInduced ... #RadiologyAssistant
Acute interstitial pneumonia (AIP, earlier named Hamman Rich Pneumonitis) is a rare idiopathic lung disease characterized
Acute interstitial ... with subsequent fibrosis ... #Clinical #Radiology ... #CTChest #AIP # ... #ILD #RadiologyAssistant