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A Case of Embolization Seen in Pulmonary Arteriovenous Malformation in a Patient with Osler-Rendu-Weber Syndrome
Korean Circulation Journal ; : 820-822, 2006.
Article in English | WPRIM | ID: wpr-197265
ABSTRACT
Osler-Rendu-Weber Syndrome or hereditary hemorrhagic telangiectasia (HHT) is characterized by telangiectasia of the skin and of the mucous membranes and intermittent bleeding from vascular abnormalities; in about 20% of the patients pulmonary arteriovenous malformation is present. Pulmonary arteriovenous malformation is a congenital anomaly in the lung which causes shunting of venous blood in the pulmonary artery to systemic circulation, resulting in cyanosis, polycythemia and clubbing. Recently we experienced a case of multiple pulmonary arteriovenous malformation associated with the telangiectatic change of the cerebral artery in a 16-year-old male patient, which was confirmed by pulmonary angiography.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Polycythemia / Arteriovenous Malformations / Pulmonary Artery / Skin / Telangiectasia, Hereditary Hemorrhagic / Telangiectasis / Angiography / Cerebral Arteries / Cyanosis / Hemorrhage Limits: Adolescent / Humans / Male Language: English Journal: Korean Circulation Journal Year: 2006 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Polycythemia / Arteriovenous Malformations / Pulmonary Artery / Skin / Telangiectasia, Hereditary Hemorrhagic / Telangiectasis / Angiography / Cerebral Arteries / Cyanosis / Hemorrhage Limits: Adolescent / Humans / Male Language: English Journal: Korean Circulation Journal Year: 2006 Type: Article