2019
DOI: 10.1016/j.clinimag.2019.07.003
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Progression of probable UIP and UIP on HRCT

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Cited by 12 publications
(14 citation statements)
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“…Analysis of extent of high density areas allows the radiologist to provide a visual quantification of the amount of fibrosis ( 21 ). A grading system can provide a visual quantification of fibrosis ( 22 ). Follow up imaging can be used to assess the extent of conversion of normal lung to fibrotic lung.…”
Section: Usual Interstitial Pneumonitis (Uip)mentioning
confidence: 99%
See 1 more Smart Citation
“…Analysis of extent of high density areas allows the radiologist to provide a visual quantification of the amount of fibrosis ( 21 ). A grading system can provide a visual quantification of fibrosis ( 22 ). Follow up imaging can be used to assess the extent of conversion of normal lung to fibrotic lung.…”
Section: Usual Interstitial Pneumonitis (Uip)mentioning
confidence: 99%
“…Thirty five patients had HC on the initial CT scan of which 57% increased the extent of disease over 31 months, also progressive disease. Enlarged pulmonary artery and emphysema were associated with disease progression ( 22 ). Serial imaging is used to evaluate progression which is not necessarily discovered between the first and second HRCT scans.…”
Section: Usual Interstitial Pneumonitis (Uip)mentioning
confidence: 99%
“…62 In terms of the progression of the disease, a study by Salvatore et al intended to determine patterns of progression in patients with probable UIP patterns. 63 They reviewed clinical information for 103 patients with a working diagnosis of IPF. They found that among patients with an initial diagnosis of probable UIP, 47% of them progressed to a definite diagnosis of UIP.…”
Section: Usual Interstitial Pneumoniamentioning
confidence: 99%
“…Combined pulmonary fibrosis and emphysema is an important radiographic diagnosis with significant centrilobular type emphysema and a UIP pattern (59). Radiologists should describe these findings as they are associated with an increased risk of lung cancer and will likely progress over time (60).…”
Section: Pulmonary Fibrosismentioning
confidence: 99%