6 results
The idiopathic interstitial pneumonias (IIPs) comprise a heterogenous group of disorders. 
They represent fundamental responses of
combinations of fibrosis ... of NSIP, UIP, OP ... and LIP have been ... #Diagnosis #Radiology ... #Pulmonary #CTChest
UIP with honeycombing (left) and chronic HP (right)
Differential diagnosis of Hypersensitivity Pneumonitis.
Subacute stage:
- RB-ILD: seen in
UIP with honeycombing ... Chronic stage: - UIP ... - UIP has a strong ... #Radiology #CTChest ... #UIP #Comparison
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 ... artifact); (G) UIP ... #Clinical #Diagnosis ... #Findings
The predominant finding is ground glass opacity (GGO).
There is very subtle traction bronchiectasis, indicating that the
The predominant finding ... the result of fibrosis ... distribution of UIP ... common interstitial lung ... #ILD #RadiologyAssistant
The predominant finding is ground glass opacity (GGO).
There is very subtle traction bronchiectasis, indicating that the
The predominant finding ... the result of fibrosis ... distribution of UIP ... common interstitial lung ... #ILD #RadiologyAssistant
Acute interstitial pneumonia (AIP, earlier named Hamman Rich Pneumonitis) is a rare idiopathic lung disease characterized
interstitial pneumonia (AIP ... rare idiopathic lung ... with subsequent fibrosis ... AIP. ... #ILD #RadiologyAssistant