Volume 21, Issue 1 640419 pp. 23-24
Open Access

Diffuse Pulmonary Ossification as a Rare Cause of Interstitial Lung Disease

Andrew Burkett

Corresponding Author

Andrew Burkett

Division of Respiratory Medicine The Ottawa Hospital Ottawa Ontario, Canada , ottawahospital.on.ca

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Niamh Coffey

Niamh Coffey

Department of Medical Imaging The Ottawa Hospital Ottawa Ontario, Canada , ottawahospital.on.ca

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Nha Voduc

Nha Voduc

Division of Respiratory Medicine The Ottawa Hospital Ottawa Ontario, Canada , ottawahospital.on.ca

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First published: 01 January 2014
Citations: 14

Abstract

Diffuse pulmonary ossification (DPO) is a rare form of interstitial lung disease. The present article describes a case of DPO in an elderly man who presented with progressive dyspnea on exertion and an isolated reduction in diffusing capacity for carbon monoxide. DPO may occur as sequelae of mitral stenosis, left heart failure, idiopathic pulmonary fibrosis, recurrent aspiration pneumonia, solid organ transplant, adult respiratory distress syndrome or may arise idiopathically. In the absence of other findings of interstitial lung disease, a lung biopsy is unlikely to be helpful in the management of these patients.

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