Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Añadir filtros








Intervalo de año
1.
Korean Journal of Radiology ; : 132-137, 2013.
Artículo en Inglés | WPRIM | ID: wpr-44582

RESUMEN

CT scans in four cases of chronic superior vena cava or left brachiocephalic vein obstruction demonstrate a systemic-to-cardiac collateral venous pathway through anastomoses between the pericardial branches of systemic veins and the presumed adventitial veins of the ascending aorta and pulmonary trunk. These adventitial veins then drain into tributaries of the anterior cardiac veins or ventricular coronary veins.


Asunto(s)
Anciano , Humanos , Masculino , Venas Braquiocefálicas/anomalías , Circulación Colateral , Medios de Contraste , Anomalías de los Vasos Coronarios/diagnóstico por imagen , Síndrome de la Vena Cava Superior/diagnóstico por imagen , Tomografía Computarizada por Rayos X
2.
Korean Circulation Journal ; : 726-731, 1994.
Artículo en Coreano | WPRIM | ID: wpr-18064

RESUMEN

Behcet's syndrome has been known as multisystemic disease caused by nonspecific immune mediated vasculitis, but it's precise etiology is not yet identified. Among the various systemic manifestations, pericardial effusion is extremely rare, and pericardial tamponade caused by massive pericardial effusion in Behcet'sydrome has not been reported in the literature. We report a case of Behcet's syndrome manifested as SVC syndrome due to SVC and right atrial thrombus with massive pericardial effusion resulting cardiac tamponade with the review of the literature.


Asunto(s)
Síndrome de Behçet , Taponamiento Cardíaco , Derrame Pericárdico , Síndrome de la Vena Cava Superior , Trombosis , Vasculitis , Vena Cava Superior
3.
Korean Circulation Journal ; : 946-952, 1993.
Artículo en Coreano | WPRIM | ID: wpr-11298

RESUMEN

The clinical triad of relapsing iritis, ulcers of the mouth and genitalia was first described in 1939 by Hulusi Behcet. This entity, originally confined to the above triad of symptoms appears to be systemic disease manifested by skin lesion, thrombophlebitis, neurologic, cardiovascular or visceral symptoms. The vascular involvement in Behcet's syndrome has been reported since Mischima first described a case in 1961, four types of vascular lesion are freuqnetly observed most commonly on the inferior or superior vena cava. Treatments consist of anticoagulation and administering oral steroids. We report a case of SVC obstruction in 36 years old female patient with Behcet's syndrome.


Asunto(s)
Adulto , Femenino , Humanos , Síndrome de Behçet , Genitales , Iritis , Boca , Piel , Esteroides , Tromboflebitis , Úlcera , Vena Cava Superior
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA