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Acquired Portosystemic Shunts in Cirrhosis and Portal Vein Thrombosis: A Case Report

Acquired portosystemic shunts (PSS) are abnormal blood vessels that develop between the portal vein and systemic circulation as a result of portal hypertension. Recurrent hyperammonemic encephalopathy in our 62-year-old patient with cirrhosis and chronic portal vein thrombosis led to the discovery o...

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Autores principales: Durgham, Anthony, Tessier, Steven, Ido, Firas, Longo, Santo, Nanda, Sudip
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9757660/
https://www.ncbi.nlm.nih.gov/pubmed/36540491
http://dx.doi.org/10.7759/cureus.31587
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author Durgham, Anthony
Tessier, Steven
Ido, Firas
Longo, Santo
Nanda, Sudip
author_facet Durgham, Anthony
Tessier, Steven
Ido, Firas
Longo, Santo
Nanda, Sudip
author_sort Durgham, Anthony
collection PubMed
description Acquired portosystemic shunts (PSS) are abnormal blood vessels that develop between the portal vein and systemic circulation as a result of portal hypertension. Recurrent hyperammonemic encephalopathy in our 62-year-old patient with cirrhosis and chronic portal vein thrombosis led to the discovery of an extremely rare and functioning portosystemic shunt (PSS). The PSS connected the inferior mesenteric and left renal veins. Such shunts are considered pathological structures and may require surgical intervention. The large PSS reported herein likely provided decompression of the portal hypertension. The concurrence of portal vein thrombosis clearly precluded any consideration of surgery. Therapeutic management in each instance of these shunts requires a full understanding of their origination, location, and physiologic implications.
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spelling pubmed-97576602022-12-19 Acquired Portosystemic Shunts in Cirrhosis and Portal Vein Thrombosis: A Case Report Durgham, Anthony Tessier, Steven Ido, Firas Longo, Santo Nanda, Sudip Cureus Gastroenterology Acquired portosystemic shunts (PSS) are abnormal blood vessels that develop between the portal vein and systemic circulation as a result of portal hypertension. Recurrent hyperammonemic encephalopathy in our 62-year-old patient with cirrhosis and chronic portal vein thrombosis led to the discovery of an extremely rare and functioning portosystemic shunt (PSS). The PSS connected the inferior mesenteric and left renal veins. Such shunts are considered pathological structures and may require surgical intervention. The large PSS reported herein likely provided decompression of the portal hypertension. The concurrence of portal vein thrombosis clearly precluded any consideration of surgery. Therapeutic management in each instance of these shunts requires a full understanding of their origination, location, and physiologic implications. Cureus 2022-11-16 /pmc/articles/PMC9757660/ /pubmed/36540491 http://dx.doi.org/10.7759/cureus.31587 Text en Copyright © 2022, Durgham et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Gastroenterology
Durgham, Anthony
Tessier, Steven
Ido, Firas
Longo, Santo
Nanda, Sudip
Acquired Portosystemic Shunts in Cirrhosis and Portal Vein Thrombosis: A Case Report
title Acquired Portosystemic Shunts in Cirrhosis and Portal Vein Thrombosis: A Case Report
title_full Acquired Portosystemic Shunts in Cirrhosis and Portal Vein Thrombosis: A Case Report
title_fullStr Acquired Portosystemic Shunts in Cirrhosis and Portal Vein Thrombosis: A Case Report
title_full_unstemmed Acquired Portosystemic Shunts in Cirrhosis and Portal Vein Thrombosis: A Case Report
title_short Acquired Portosystemic Shunts in Cirrhosis and Portal Vein Thrombosis: A Case Report
title_sort acquired portosystemic shunts in cirrhosis and portal vein thrombosis: a case report
topic Gastroenterology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9757660/
https://www.ncbi.nlm.nih.gov/pubmed/36540491
http://dx.doi.org/10.7759/cureus.31587
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