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1.
J. Transcatheter Interv ; 31: eA20220020, 2023. ilustração
Artigo em Inglês, Português | LILACS-Express | LILACS | ID: biblio-1413942

RESUMO

Malformações arteriovenosas pulmonares são uma comunicação anormal entre uma artéria e uma veia, causando manifestações clínicas, como hipoxemia crônica e eventos embólicos. As malformações arteriovenosas eram tratadas cirurgicamente, com taxa expressiva de complicações. Na década de 1970, a primeira embolização percutânea por cateter foi realizada com molas. Descrevemos três casos nos quais técnicas de embolização percutânea foram efetivas em prevenir eventos embólicos, hemorrágicos e hipoxêmicos no seguimento dos pacientes.


Pulmonary arteriovenous malformation is an abnormal communication between an artery and a vein, causing clinical manifestations, such as chronic hypoxemia and embolic events. Arteriovenous malformations were treated surgically, with a significant rate of complications. In the 1970 ́s, the first percutaneous catheter embolization was performed with coils. We describe three cases in which percutaneous embolization techniques were effective to prevent embolic, hemorrhagic, and hypoxemic events in the follow-up of patients.

2.
Journal of the Korean Radiological Society ; : 503-506, 1999.
Artigo em Coreano | WPRIM | ID: wpr-101847

RESUMO

Hereditary hemorrhagic telangiectasia (HHT) or Osler-Weber-Rendu disease is an autosomal dominant disorder characterized by repeated episodes of bleeding. Multiple telangiectases consisting of thin-walled, dilated vascular channels with arteriovenous communication may involve, for example, mucocutaneous tissue, the gastrointestinal tract, and the liver, lung, and brain. We report the imaging findings of two cases of HHT involving arteriovenous malformation of both the lungs and liver, a rare condition. Chest radiography revealed a round mass, while helical CT showed a feeding artery and draining vein with arteriovenous malformation in the lung. Color Doppler sonography revealed an enlarged and tortuous hepatic artery with high systolic velocity. CT demonstrated an enlarged hepatic artery, arteriovenous shunt, and early draining hepatic vein in the liver. Celiac angiography showed arteriovenous malformation.


Assuntos
Angiografia , Artérias , Malformações Arteriovenosas , Encéfalo , Trato Gastrointestinal , Hemorragia , Artéria Hepática , Veias Hepáticas , Fígado , Pulmão , Radiografia , Telangiectasia Hemorrágica Hereditária , Telangiectasia , Tórax , Tomografia Computadorizada Espiral , Veias
3.
Journal of the Korean Radiological Society ; : 595-598, 1996.
Artigo em Coreano | WPRIM | ID: wpr-194378

RESUMO

Pulmonary arteriovenous malformation(PAVM) are associated with substantial risks if left untreated. The literature reports a 40-50% incidence of paradoxical embolization. Percutaneous arterial embolization has become the standard treatemtn for PAVM. We report a case of pulmonary arteriovenous malformation successfully treated bytranscatheter embolization using detachable balloons and we also demonstrate long-term follow up CT findings.


Assuntos
Malformações Arteriovenosas , Seguimentos , Incidência
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