Journal of Thoracic Imaging · 2007 · 72 citations · 11 references
Medical ImagingOphthalmologyAdvanced Lung DiseaseSystemic SclerodermaSystemic SclerosisVascular ImagingGround GlassGround-glass OpacityRadiologic ImagingSclerodermaMedicineLong-term Follow-upRadiologyHealth Sciences
Despite little supportive evidence, ground-glass opacity at high-resolution computed tomography, without other signs of fibrosis, has been equated with potentially reversible disease, and in systemic sclerosis, frequently prompts aggressive anti-inflammatory treatment to prevent pulmonary fibrosis. Our study evaluates ground-glass opacity on sequential high-resolution computed tomography in 41 patients with systemic sclerosis over a mean follow-up period of 27 months (r6 to 60 mo). Ground-glass opacity was the most common imaging finding, present in 66%, and usually associated with other signs of interstitial disease, including nonfibrotic interstitial opacities in 27% and fibrotic interstitial opacities in 32%. Improvement was only documented in 2(5%) patients with ground glass and nonfibrotic interstitial opacities. In systemic sclerosis, ground-glass opacity is most commonly associated with irreversible disease. Disease progression or improvement could not be predicted by the presence of ground-glass opacity.
11
Disease activity in idiopathic pulmonary fibrosis: CT and pathologic correlation.
Néstor L. Müller, C A Staples, Roberta R. Miller et al. · Radiology · 1987 · 207 citations