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.
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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