7 results
The idiopathic interstitial pneumonias (IIPs) comprise a heterogenous group of disorders. 
They represent fundamental responses of
combinations of fibrosis ... arthritis findings of NSIP ... , UIP, OP and LIP ... #Diagnosis #Radiology ... #Pulmonary #CTChest
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 ... Correlation #Table #ILD
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 ... #Clinical #Diagnosis ... #UIP #Comparison
The predominant finding is ground glass opacity (GGO).
There is very subtle traction bronchiectasis, indicating that the
the result of fibrosis ... distribution of UIP ... 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 ... distribution of UIP ... common interstitial lung ... #Clinical #Radiology ... #CTChest #NSIP
Cavities frequently arise within a mass or an area of consolidation as a result of necrosis.
We
the surrounding lung ... fibrosis (11). ... #Clinical #Diagnosis ... #Radiology #CTChest ... Cyst #Emphysema #Comparison
Acute interstitial pneumonia (AIP, earlier named Hamman Rich Pneumonitis) is a rare idiopathic lung disease characterized
rare idiopathic lung ... with subsequent fibrosis ... AIP. ... #Clinical #Radiology ... #CTChest #AIP #