14 results
Typical UIP with honeycombing and traction bronchiectasis in a patient with idiopathic pulmonary fibrosis (IPF) #Clinical
Typical UIP with ... idiopathic pulmonary fibrosis ... (IPF) #Clinical ... #Radiology #CTChest ... #UIP #IPF #ILD
Differential diagnosis of Langerhans cell histiocytosis.
Nodular LCH:
- Sarcoidosis: perilymphatic distribution.
- Metastases: random distribution.
Cystic LCH:
- LAM: round
: 'signet ring sign ... central dot. - LIP ... #Clinical #Diagnosis ... #Radiology #CTChest ... #Cystic #Cysts
HRCT findings in UIP
Honeycombing consisting of multilayered thick-walled cysts.
Architectural distortion with traction bronchiectasis due to fibrosis.
Predominance
HRCT findings in UIP ... multilayered thick-walled cysts ... lymphadenopathy #Clinical ... #Radiology #CTChest ... #UIP #UsualInterstitialPneumonitis
On the left a chest film of a patient with UIP due to IPF.
The findings on
a patient with UIP ... preference also think 'UIP ... #Clinical #Radiology ... #CXR #CTChest # ... UIP #UsualInterstitialPneumonitis
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
On the left a patient with DIP.
The HRCT shows diffuse areas of ground-glass density in the
a patient with DIP ... abnormalities and signs ... of fibrosis are ... #Radiology #CTChest ... #DIP #DesquamativeInterstitialPneumonia
UIP
UIP is a histologic pattern of pulmonary fibrosis.
On a chest X-ray UIP manifests as a reticular
UIP UIP is a histologic ... UIP manifests as ... you can suspect UIP ... #Clinical #Radiology ... #CXR #UIP #Reticular
Honeycombing represents the second reticular pattern recognizable on HRCT.
Because of the cystic appearance, honeycombing is also
composed of dense fibrous ... interstitial pneumonia (UIP ... #Clinical #Radiology ... #CTChest #Honeycombing ... #UIP #UsualInterstitialPneumonia
Acute interstitial pneumonia (AIP, earlier named Hamman Rich Pneumonitis) is a rare idiopathic lung disease characterized
interstitial pneumonia (AIP ... HRCT findings in AIP ... the diagnosis AIP ... #Clinical #Radiology ... #CTChest #AIP #
The predominant finding is ground glass opacity (GGO).
There is very subtle traction bronchiectasis, indicating that the
the result of fibrosis ... distribution of UIP ... #Clinical #Radiology ... #CTChest #NSIP ... NonspecificInterstitialPneumonia #ILD