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The Journal of Thoracic and Cardiovascular Surgery, Vol 83, 285-289, Copyright © 1982 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
SE Brown, PW Wright, JW Renner and JB Riker
A patient with hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu
syndrome) with multiple bilateral pulmonary arteriovenous malformations was
hypoxic, cyanotic, polycythemic, and severely limited by dyspnea on
exertion. Following staged bilateral thoracotomies, with removal of 23
major fistulas (12 from the right lung and 11 from the left), marked
improvement in symptoms, blood gases, and objective measurements of
exercise tolerance occurred.
ARTICLES
Staged bilateral thoracotomies for multiple pulmonary arteriovenous malformations complicating hereditary hemorrhagic telangiectasia
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