9 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 ... artifact); (G) UIP ... #Clinical #Diagnosis ... Correlation #Table #ILD
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 ... IdiopathicInterstitialPneumonia #ILD
UIP with honeycombing (left) and chronic HP (right)
Differential diagnosis of Hypersensitivity Pneumonitis.
Subacute stage:
- RB-ILD: seen in
) Differential diagnosis ... smokers, upper lobe ... throughout the whole lung ... #Clinical #Diagnosis ... #Radiology #CTChest
The predominant finding is ground glass opacity (GGO).
There is very subtle traction bronchiectasis, indicating that the
the result of fibrosis ... distribution of UIP ... suggestive for the diagnosis ... common interstitial lung ... #Clinical #Radiology
The predominant finding is ground glass opacity (GGO).
There is very subtle traction bronchiectasis, indicating that the
the result of fibrosis ... distribution of UIP ... suggestive for the diagnosis ... common interstitial lung ... #Clinical #Radiology
On the left a chest film of a patient with UIP due to IPF.
The findings on
volume loss and fibrotic ... changes in the basal lung ... reticulation with a lower lobe ... #Clinical #Radiology ... Pneumonitis #Reticular #ILD
On the left a patient who is treated with cytotoxic drugs for a hematologic malignancy.
The radiographic
the left lower lobe ... patients with a UIP ... pattern or NSIP ... consider drug-related lung ... #Clinical #Radiology
CT and ultrasonographic features of COVID-19 pneumonia
Lung CT:
 - Thickened pleura
 - Ground glass shadow and
ultrasonographic features of COVID ... More than two lobes ... ultrasound - ... with pulmonary fibrosis ... POCUS #features #Radiology
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 ... AcuteInterstitialPneumonia #ILD