11 results
High Attenuation pattern (2) 
1. Non specific interstitial pneumonitis (NSIP): ground glass with traction bronchiectasis, no
(NSIP): ground ... #Clinical #Radiology ... #HRCT #CTChest ... #Comparison #Table ... #RadiologyAssistant
Nodular pattern
1. Hypersensitivity pneumonitis: ill defined centrilobular nodules.
2. Miliary TB: random nodules
3. Sarcoidosis: nodules with perilymphatic
: ill defined centrilobular ... #Clinical #Radiology ... #HRCT #CTChest ... #Comparison #Table ... #RadiologyAssistant
UIP with honeycombing (left) and chronic HP (right)
Differential diagnosis of Hypersensitivity Pneumonitis.
Subacute stage:
- RB-ILD: seen in
Pneumonitis. ... #Clinical #Diagnosis ... #Radiology #CTChest ... #UIP #Comparison ... #ILD #RadiologyAssistant
Ground-glass opacity
Ground-glass opacity (GGO) represents:
- Filling of the alveolar spaces with pus, edema, hemorrhage, inflammation or
resolution of the HRCT ... in ground glass pattern ... , NSIP, DIP. - Centrilobular ... #CTChest #GGO # ... #RadiologyAssistant
The idiopathic interstitial pneumonias (IIPs) comprise a heterogenous group of disorders. 
They represent fundamental responses of
idiopathic interstitial pneumonias ... combinations of fibrosis ... listed in the table ... #Diagnosis #Radiology ... #Pulmonary #CTChest
On the left some diseases with a nodular pattern.
1. Hypersensitivity pneumonitis: ill defined centrilobular nodules.
2. Miliary
#Clinical #Diagnosis ... #CTChest #Nodular ... #Differential # ... Comparison #Table ... #RadiologyAssistant
On the left a patient with ground glass pattern in a mosaic distribution.
Some lobules are involved
with ground glass pattern ... The differential ... are confluent, HRCT ... #Clinical #Radiology ... #CTChest #GGO #
Chronic hypersensitivity pneumonitis (2)
The case on the left shows an inspiratory and expiratory scan: the mosaic
included in the differential ... #Clinical #Radiology ... #CTChest #Chronic ... #HypersensitivityPneumonitis ... #Fibrosis #RadiologyAssistant
Acute interstitial pneumonia (AIP, earlier named Hamman Rich Pneumonitis) is a rare idiopathic lung disease characterized
named Hamman Rich Pneumonitis ... with subsequent fibrosis ... The histologic pattern ... #Clinical #Radiology ... #CTChest #AIP #
On the left a patient who is treated with cytotoxic drugs for a hematologic malignancy.
The radiographic
pattern or NSIP ... disease in the differential ... #Clinical #Radiology ... #CTChest #DrugInduced ... #RadiologyAssistant