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Published online before print February 12, 2008, 10.1148/radiol.2471070369
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(Radiology 2008;247:251-259.)
© RSNA, 2008


Thoracic Imaging

Nonspecific Interstitial Pneumonia and Idiopathic Pulmonary Fibrosis: Changes in Pattern and Distribution of Disease over Time1

C. Isabela S. Silva, MD, PhD, Nestor L. Müller, MD, PhD, David M. Hansell, MD, Kyung S. Lee, MD, Andrew G. Nicholson, MD, and Athol U. Wells, MD

1 From the Department of Radiology, Vancouver General Hospital, University of British Columbia, 3350-950 W 10th Ave, Vancouver, BC, Canada V5Z 4E3 (C.I.S.S., N.L.M.); Department of Radiology (D.M.H.), Department of Pathology (A.G.N.), and Interstitial Lung Disease Unit (A.U.W.), Royal Brompton Hospital, London, England; and Department of Radiology and the Center for Imaging Science, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea (K.S.L.). Received February 22, 2007; revision requested May 8; revision received June 12; accepted July 18; final version accepted September 11. Address correspondence to C.I.S.S. (e-mail: isabela.silva{at}vch.ca).

Purpose: To retrospectively assess the change in disease pattern of nonspecific interstitial pneumonia (NSIP) and idiopathic pulmonary fibrosis (IPF) findings seen at thin-section computed tomography (CT) at long-term follow-up and to compare the same with initial findings at CT.

Materials and Methods: The study included 48 patients (28 men, 20 women; mean age, 57.5 years) with biopsy-proved NSIP (n = 23) or IPF (n = 25) who underwent CT at initial diagnosis and at follow-up 34–155 months later. The CT scans were randomized and reviewed by two independent thoracic radiologists for pattern and distribution of ground-glass opacity (GGO), reticulation, traction bronchiectasis and bronchiolectasis, and honeycombing. Statistical analysis was performed by using nonparametric methods and univariate logistic regression.

Results: Follow-up CT in patients with NSIP showed marked decrease in the extent of GGO, increase in reticulation, and a greater likelihood of peripheral distribution (all P < .05). At presentation, the CT findings were interpreted as suggestive of NSIP in 18 of 23 patients with NSIP and indeterminate or suggestive of IPF in five. In five (28%) of 18 patients with initial findings suggestive of NSIP, the follow-up CT scans were interpreted as more suggestive of IPF. No CT features seen at presentation allowed distinction between patients with NSIP that maintained an NSIP pattern at follow-up and those that progressed to an IPF pattern.

Conclusion: At follow-up CT, 28% of patients with initial CT findings suggestive of NSIP progressed to findings suggestive of IPF. Similar initial CT findings for NSIP may have different imaging outcomes.

© RSNA, 2008




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