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Diffuse Pulmonary Ossification as a Rare Cause of Interstitial Lung Disease
Author(s) -
Andrew Burkett,
Niamh Coffey,
Nha Voduc
Publication year - 2014
Publication title -
canadian respiratory journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.675
H-Index - 53
eISSN - 1916-7245
pISSN - 1198-2241
DOI - 10.1155/2014/640419
Subject(s) - medicine , lung biopsy , interstitial lung disease , lung , respiratory distress , diffusing capacity , rare disease , pulmonary fibrosis , diffuse alveolar damage , cardiology , pathology , disease , radiology , acute respiratory distress , lung function
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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