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Endovascular treatment of spontaneous isolated abdominal aortic dissection

Isolated abdominal aortic dissection is a rare clinical disease representing only 1.3% of all dissections. There are a few case series reported in the literature. The causes of this pathology can be spontaneous, iatrogenic, or traumatic. Most patients are asymptomatic and symptoms are usually abdomi...

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Autores principales: Giribono, Anna Maria, Ferrara, Doriana, Spalla, Flavia, Narese, Donatella, Bracale, Umberto, Pecoraro, Felice, Bracale, Renata, del Guercio, Luca, Bracale, Umberto Marcello
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5152934/
https://www.ncbi.nlm.nih.gov/pubmed/27994881
http://dx.doi.org/10.1177/2058460116681042
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author Giribono, Anna Maria
Ferrara, Doriana
Spalla, Flavia
Narese, Donatella
Bracale, Umberto
Pecoraro, Felice
Bracale, Renata
del Guercio, Luca
Bracale, Umberto Marcello
author_facet Giribono, Anna Maria
Ferrara, Doriana
Spalla, Flavia
Narese, Donatella
Bracale, Umberto
Pecoraro, Felice
Bracale, Renata
del Guercio, Luca
Bracale, Umberto Marcello
author_sort Giribono, Anna Maria
collection PubMed
description Isolated abdominal aortic dissection is a rare clinical disease representing only 1.3% of all dissections. There are a few case series reported in the literature. The causes of this pathology can be spontaneous, iatrogenic, or traumatic. Most patients are asymptomatic and symptoms are usually abdominal or back pain, while claudication and lower limb ischemia are rare. Surgical and endovascular treatment are two valid options with acceptable results. We herein describe nine cases of symptomatic spontaneous isolated abdominal aortic dissection, out of which four successfully were treated with an endovascular approach between July 2003 and July 2013. All patients were men, smokers, symptomatic (either abdominal or back pain or lower limb ischemia), with a history of high blood pressure, with a medical history negative for concomitant aneurysmatic dilatation or previous endovascular intervention. Diagnosis of isolated abdominal aortic dissection were established by contrast-enhanced computed tomography angiography (CTA) of the thoracic and abdominal aorta. All nine patients initially underwent medical treatment. In four symptomatic cases, non-responsive to medical therapy, bare-metal stents or stent grafts were successfully positioned. All patients completed a CTA follow-up of at least 12 months, during which they remained symptom-free. Endovascular management of this condition is associated with a high rate of technical success and a low mortality; therefore, it can be considered the treatment of choice when it is feasible.
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spelling pubmed-51529342016-12-19 Endovascular treatment of spontaneous isolated abdominal aortic dissection Giribono, Anna Maria Ferrara, Doriana Spalla, Flavia Narese, Donatella Bracale, Umberto Pecoraro, Felice Bracale, Renata del Guercio, Luca Bracale, Umberto Marcello Acta Radiol Open Case Report Isolated abdominal aortic dissection is a rare clinical disease representing only 1.3% of all dissections. There are a few case series reported in the literature. The causes of this pathology can be spontaneous, iatrogenic, or traumatic. Most patients are asymptomatic and symptoms are usually abdominal or back pain, while claudication and lower limb ischemia are rare. Surgical and endovascular treatment are two valid options with acceptable results. We herein describe nine cases of symptomatic spontaneous isolated abdominal aortic dissection, out of which four successfully were treated with an endovascular approach between July 2003 and July 2013. All patients were men, smokers, symptomatic (either abdominal or back pain or lower limb ischemia), with a history of high blood pressure, with a medical history negative for concomitant aneurysmatic dilatation or previous endovascular intervention. Diagnosis of isolated abdominal aortic dissection were established by contrast-enhanced computed tomography angiography (CTA) of the thoracic and abdominal aorta. All nine patients initially underwent medical treatment. In four symptomatic cases, non-responsive to medical therapy, bare-metal stents or stent grafts were successfully positioned. All patients completed a CTA follow-up of at least 12 months, during which they remained symptom-free. Endovascular management of this condition is associated with a high rate of technical success and a low mortality; therefore, it can be considered the treatment of choice when it is feasible. SAGE Publications 2016-12-05 /pmc/articles/PMC5152934/ /pubmed/27994881 http://dx.doi.org/10.1177/2058460116681042 Text en © The Foundation Acta Radiologica 2016 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page(https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Giribono, Anna Maria
Ferrara, Doriana
Spalla, Flavia
Narese, Donatella
Bracale, Umberto
Pecoraro, Felice
Bracale, Renata
del Guercio, Luca
Bracale, Umberto Marcello
Endovascular treatment of spontaneous isolated abdominal aortic dissection
title Endovascular treatment of spontaneous isolated abdominal aortic dissection
title_full Endovascular treatment of spontaneous isolated abdominal aortic dissection
title_fullStr Endovascular treatment of spontaneous isolated abdominal aortic dissection
title_full_unstemmed Endovascular treatment of spontaneous isolated abdominal aortic dissection
title_short Endovascular treatment of spontaneous isolated abdominal aortic dissection
title_sort endovascular treatment of spontaneous isolated abdominal aortic dissection
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5152934/
https://www.ncbi.nlm.nih.gov/pubmed/27994881
http://dx.doi.org/10.1177/2058460116681042
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