6 results
Figure 3 HRCT-LUS correlation in normal lung, pulmonary congestion, rheumatoid lung disease, idiopathic pulmonary fibrosis.
Notes: (A)
yellow arrow); (E) NSIP ... fibrotic lung with ... #Clinical #Diagnosis ... #HRCT #POCUS #Lung ... Correlation #Table #ILD
The idiopathic interstitial pneumonias (IIPs) comprise a heterogenous group of disorders. 
They represent fundamental responses of
combinations of fibrosis ... morphologic findings on HRCT ... 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
show very similar HRCT ... throughout the whole lung ... #Clinical #Diagnosis ... #Radiology #CTChest ... #UIP #Comparison
The predominant finding is ground glass opacity (GGO).
There is very subtle traction bronchiectasis, indicating that the
the result of fibrosis ... suggestive for the diagnosis ... common interstitial lung ... #Clinical #Radiology ... #CTChest #NSIP
The predominant finding is ground glass opacity (GGO).
There is very subtle traction bronchiectasis, indicating that the
the result of fibrosis ... suggestive for the diagnosis ... common interstitial lung ... #Clinical #Radiology ... #CTChest #NSIP
Acute interstitial pneumonia (AIP, earlier named Hamman Rich Pneumonitis) is a rare idiopathic lung disease characterized
rare idiopathic lung ... with subsequent fibrosis ... suggestive of the diagnosis ... #Clinical #Radiology ... #CTChest #AIP #