Pulmonary arteriovenous malformations associated with hereditary hemorrhagic telangiectasia are often multiple and may enlarge with time.1 Shunt-induced hypoxemia is surgically correctable when the lesions are solitary or localized to one or two lobes.2 When surgery is contraindicated the therapeutic options are limited. We wish to describe a patient with hereditary hemorrhagic telangiectasia in whom multiple balloons were embolized into eight pulmonary arteriovenous malformations to correct severe shunt-induced hypoxemia. Case Report A 55-year-old man with hereditary hemorrhagic telangiectasia noted the onset of dyspnea in January 1979 and was hospitalized for evaluation of its progression in March 1979. The chest film showed. . .
|Original language||English (US)|
|Number of pages||2|
|Journal||New England Journal of Medicine|
|State||Published - May 22 1980|
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