A Case of the Bronchial Artery-Pulmonary Vein Malformation / 결핵
Tuberculosis and Respiratory Diseases
;
: 767-771, 1995.
Artículo
en Coreano
| WPRIM
| ID: wpr-117116
ABSTRACT
The bronchial artery-pulmonary vein malformation should be called the systemic artery-to- pulmonary vein arterioveonus malformation in the lung. Although pulmonary arteriovenous malformation has been well documented in intrapulmonary arteriovenous malformation, the systemic artery-to-pulmonary vein arteriovenous malformation is rare. Most patients with systemic artery-to-pulmonary vein arteriovenous malformation is asymptomatic and the diagnosis of these anomaly may be done by continuous murmur or abnormal chest X-ray on the physical examination. The pathogenesis of this condition is congenital malformation which explains these anastomoses between the pulmonary vein and accessory brochial arteries and acquired malformation which explains development of new blood vessel to supply large enough to cause significant systemic-pulmonary shunts due to inflammation secondary to infection, trauma, or previous surgery. We experienced a case of the bronchial artery-pulmonary vein malformation which was detected on angiography in 20-year-old women whose chief complain is hemoptysis. This massive hemoptysis was controlled by selective brochial artery embolization with Gelfoam and Ivalon particles.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Examen Físico
/
Arterias
/
Malformaciones Arteriovenosas
/
Venas Pulmonares
/
Tórax
/
Venas
/
Vasos Sanguíneos
/
Angiografía
/
Diagnóstico
/
Esponja de Gelatina Absorbible
Tipo de estudio:
Estudio diagnóstico
Límite:
Femenino
/
Humanos
Idioma:
Coreano
Revista:
Tuberculosis and Respiratory Diseases
Año:
1995
Tipo del documento:
Artículo
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