Purpose:To investigate the prevalence of diffuse pulmonary ossification (DPO) in patients with fibrosing interstitial lung disease (ILD) and determine whether there are differences among the types of ILDs.
Materials and Methods:Institutional review board approval was given and patient consent was not required for this study.
Results:In the whole population, the prevalence of DPO was 166 (18.6%) and 106 (11.9%) of 892 patients according to definitions 1 and 2, respectively. The prevalence of DPO (definition 1) was significantly higher in patients with IPF (28.5%) than in those without IPF (8.3%, P , .001). Nine of 192 (4.7%) had chronic hypersensitivity pneumonitis (P , .001), and 27 of 244 (11.1%) had nonspecific interstitial pneumonia (P , .001). At multivariate analysis, DPO according to definition 1 was an independent predictor of IPF diagnosis (P , .001) and male sex (P = .003).Coarseness of fibrosing ILD (P = .011) and IPF diagnosis (P = .016) were independently associated with pulmonary ossification profusion.
Conclusion:DPO is common in patients with fibrosing ILD and is significantly more prevalent in patients with IPF than in those with other fibrosing ILDs, and thus, computed tomographic signs of DPO may be helpful for diagnosis of IPF.q RSNA, 2017