A Case of Hepatic Involvement in Hereditary Hemorrhagic Telangiectasia Presenting as High Output Heart Failure / 계명의대학술지
Keimyung Medical Journal
; : 204-208, 2015.
Article
Dans Ko
| WPRIM
| ID: wpr-12450
Responsable en Bibliothèque :
WPRO
ABSTRACT
Hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Weber-Rendu disease, is a rare autosomal dominant vascular disorder involving arteriovenous malformation. HHT is characterized by recurrent epistaxis, cutaneous telangiectasia, and visceral arteriovenous malformations. Hepatic arteriovenous malformation can lead to high output heart failure. We report a case of hereditary hemorrhagic telangiectasia patient who complained dyspnea and edema on both lower extremity.
Texte intégral:
1
Indice:
WPRIM
Sujet Principal:
Malformations artérioveineuses
/
Télangiectasie hémorragique héréditaire
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Télangiectasie
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Épistaxis
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Membre inférieur
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Dyspnée
/
Oedème
/
Coeur
/
Défaillance cardiaque
Limites du sujet:
Humans
langue:
Ko
Texte intégral:
Keimyung Medical Journal
Année:
2015
Type:
Article