Síndrome aórtico agudo. Revisión de la literatura y actualización del tema
Author
dc.contributor.author
Vega S., Javier
Author
dc.contributor.author
Zamorano G., Jaime
es_CL
Author
dc.contributor.author
Pereira C., Nicolás
es_CL
Author
dc.contributor.author
Galleguillos G., Alfonso
es_CL
Admission date
dc.date.accessioned
2015-01-08T02:30:25Z
Available date
dc.date.available
2015-01-08T02:30:25Z
Publication date
dc.date.issued
2014
Cita de ítem
dc.identifier.citation
Rev Med Chile 2014; 142: 344-352
en_US
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/124317
General note
dc.description
Artículo de publicación SciELO
en_US
Abstract
dc.description.abstract
Acute aortic syndrome (AAS) is a term that describes interrelated aortic
emergencies with similar clinical characteristics and challenges. These are aortic
dissection (AD), intramural hematoma (IH), and penetrating atherosclerotic
ulcer (PAU). The incidence of AAS is three cases per 100.000 persons per year.
Diverse genetic disorders and acquired conditions have been related to the
pathogenesis of this disease. Clinical features of patients with any of the three
conditions comprising AAS are very similar. A high degree of clinical suspicion
and imaging studies are necessary for an accurate diagnosis. Prognosis is clearly
related to underlying diagnosis and appropriate surgical repair, in the case of
proximal involvement of the aorta. Involvement of distal segments of the aorta
may require medical or endovascular therapy according to the presence of complications.
After hospital discharge, patients require lifelong follow-up.