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A 70-year-old woman with rapidly progressive interstitial lung disease associated with clinically amyopathic dermatomyositis (antibody unknown). HRCT images (a,b) show diffuse ground-glass opacification and consolidation just below the pleura. Crazy-paving appearance, interlobular septal thickening and bilateral pleural effusions are also seen. The patient died 2 weeks after admission.
