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Fig. 6B —68-year-old man with biopsy-proven idiopathic pulmonary fibrosis (IPF). Low-power view of autopsy specimen shows severe fibrosis and honeycombing consistent with idiopathic pulmonary fibrosis. Microscopic findings were characteristic of usual interstitial pneumonia; there was no microscopic evidence of hypersensitivity pneumonitis. (H and E, x10)