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Interstitial pulmonary fibrosis is a rare, diffuse lug disease which has a tendency to destroy the lung
architectures by consequent healing with progressively severe fibrosis.
We report with a brief review of literature, one case of a 7-year old female with the typical pictures
of interstitial pulmonary fibrosis, histologically on open lung biopsy, and clinically presenting with
chronic respiratory difficulty but without definite symptoms... |
