Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/43653
Title: Hereditary Hemorrhagic Telangiectasia and Myocardial Infarction
Authors: Martínez-Quintana, Efrén 
Rodríguez-González, Fayna
Gopar-Gopar, Silvia
UNESCO Clasification: 320501 Cardiología
Keywords: Hereditary hemorrhagic teangiectasi
Osler–Weber–Rendu syndrome
Pulmonary arteriovenous malformations
Myocardial infarction
Issue Date: 2016
Publisher: 1061-1711
Journal: International Journal of Angiology 
Abstract: Hereditary hemorrhagic telangiectasia, also known as Osler–Weber–Rendu syndrome, is an autosomal dominant genetic disorder that leads to epistaxis, gastrointestinal bleeding, iron deficiency anemia, and arteriovenous malformations at the lungs, the liver, and the brain. However, due to its rarity and its unspecific findings on routine examinations, diagnosis is not easy unless suspected due to hypoxemia or paradoxical embolism. We present a case of a 46-year-old-woman with hereditary hemorrhagic telangiectasia and hypoxemia who presented a myocardial infarction secondary to paradoxical embolism through pulmonary arteriovenous malformations.
URI: http://hdl.handle.net/10553/43653
ISSN: 1061-1711
DOI: 10.1055/s-0035-1551795
Source: International Journal of Angiology [ISSN 1061-1711], v. 25, p. e81-e83
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