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Management with right atrium to jugular and brachiocephalic vein bypass for dialysis catheter-related superior vena cava syndrome

Superior vena cava (SVC) syndrome is a spectrum of potentially life-threatening clinical manifestations resulting from either partial or complete obstruction of central venous blood flow. Approximately 70% of cases are caused by malignancy. The primary treatment end point for SVC syndrome is the ach...

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Detalles Bibliográficos
Autores principales: Nguyen, Daniel, Berman, Scott S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10522989/
https://www.ncbi.nlm.nih.gov/pubmed/37771730
http://dx.doi.org/10.1016/j.jvscit.2023.101306
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author Nguyen, Daniel
Berman, Scott S.
author_facet Nguyen, Daniel
Berman, Scott S.
author_sort Nguyen, Daniel
collection PubMed
description Superior vena cava (SVC) syndrome is a spectrum of potentially life-threatening clinical manifestations resulting from either partial or complete obstruction of central venous blood flow. Approximately 70% of cases are caused by malignancy. The primary treatment end point for SVC syndrome is the achievement of long-term patency of the SVC. Malignant SVC syndrome is managed by either radiation therapy, open surgical intervention, or endovascular therapy with angioplasty and stenting. The current report describes an uncommon case of nonmalignant SVC syndrome resulting from complications of hemodialysis catheters that was managed with open revascularization between the right internal jugular and brachiocephalic veins and the right atrium.
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spelling pubmed-105229892023-09-28 Management with right atrium to jugular and brachiocephalic vein bypass for dialysis catheter-related superior vena cava syndrome Nguyen, Daniel Berman, Scott S. J Vasc Surg Cases Innov Tech Case report Superior vena cava (SVC) syndrome is a spectrum of potentially life-threatening clinical manifestations resulting from either partial or complete obstruction of central venous blood flow. Approximately 70% of cases are caused by malignancy. The primary treatment end point for SVC syndrome is the achievement of long-term patency of the SVC. Malignant SVC syndrome is managed by either radiation therapy, open surgical intervention, or endovascular therapy with angioplasty and stenting. The current report describes an uncommon case of nonmalignant SVC syndrome resulting from complications of hemodialysis catheters that was managed with open revascularization between the right internal jugular and brachiocephalic veins and the right atrium. Elsevier 2023-08-28 /pmc/articles/PMC10522989/ /pubmed/37771730 http://dx.doi.org/10.1016/j.jvscit.2023.101306 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case report
Nguyen, Daniel
Berman, Scott S.
Management with right atrium to jugular and brachiocephalic vein bypass for dialysis catheter-related superior vena cava syndrome
title Management with right atrium to jugular and brachiocephalic vein bypass for dialysis catheter-related superior vena cava syndrome
title_full Management with right atrium to jugular and brachiocephalic vein bypass for dialysis catheter-related superior vena cava syndrome
title_fullStr Management with right atrium to jugular and brachiocephalic vein bypass for dialysis catheter-related superior vena cava syndrome
title_full_unstemmed Management with right atrium to jugular and brachiocephalic vein bypass for dialysis catheter-related superior vena cava syndrome
title_short Management with right atrium to jugular and brachiocephalic vein bypass for dialysis catheter-related superior vena cava syndrome
title_sort management with right atrium to jugular and brachiocephalic vein bypass for dialysis catheter-related superior vena cava syndrome
topic Case report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10522989/
https://www.ncbi.nlm.nih.gov/pubmed/37771730
http://dx.doi.org/10.1016/j.jvscit.2023.101306
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