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Chest, Vol 89, 760-762, Copyright © 1986 by American College of Chest Physicians
ARTICLES |
EA Streeten, SM de la Monte and TP Kennedy
Respiratory involvement with amyloidosis typically involves the tracheobronchial tree or lung parenchyma. We describe a patient with systemic amyloidosis who was respirator-dependent because of extensive amyloid infiltration of the diaphragm, with no evidence of other pulmonary amyloidosis. Diaphragmatic myopathy from amyloid should be considered in respiratory failure in amyloidosis.
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