7 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
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 ... #Clinical #Radiology ... #CTChest #NSIP
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 ... #Clinical #Radiology ... #CTChest #NSIP
On the left a patient who is treated with cytotoxic drugs for a hematologic malignancy.
The radiographic
The radiographic findings ... patients with a UIP ... pattern or NSIP ... #Clinical #Radiology ... #RadiologyAssistant
Acute interstitial pneumonia (AIP, earlier named Hamman Rich Pneumonitis) is a rare idiopathic lung disease characterized
(AIP, earlier named ... rare idiopathic lung ... the diagnosis AIP ... #Clinical #Radiology ... #CTChest #AIP #
Chronic hypersensitivity pneumonitis (2)
The case on the left shows an inspiratory and expiratory scan: the mosaic
Signs of fibrosis ... mid and lower lung ... #Clinical #Radiology ... #CTChest #Chronic ... #Fibrosis #RadiologyAssistant