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Hereditary Hemorrhagic Telangiectasia and Refractory Ascites

Hereditary hemorrhagic telangiectasia is a rare autosomal dominant disease that can involve the liver. The presence of arteriohepatic venous shunts can lead to high output cardiac failure and biliary ischemia, whereas arterioportal venous shunts can result in portal hypertension. Cirrhosis and nodul...

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Detalles Bibliográficos
Autores principales: Thandassery, Ragesh B., Patel, Rahul S., Grewal, Priya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7556362/
https://www.ncbi.nlm.nih.gov/pubmed/33134402
http://dx.doi.org/10.14309/crj.0000000000000458
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author Thandassery, Ragesh B.
Patel, Rahul S.
Grewal, Priya
author_facet Thandassery, Ragesh B.
Patel, Rahul S.
Grewal, Priya
author_sort Thandassery, Ragesh B.
collection PubMed
description Hereditary hemorrhagic telangiectasia is a rare autosomal dominant disease that can involve the liver. The presence of arteriohepatic venous shunts can lead to high output cardiac failure and biliary ischemia, whereas arterioportal venous shunts can result in portal hypertension. Cirrhosis and nodular regenerative hyperplasia are also reported in these patients. Management of these patients in the setting of symptomatic liver disease is challenging. Transarterial embolization and hepatic artery ligation are usually considered palliative options. In selected cases, orthotopic liver transplantation can cure both liver disease and heart failure.
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spelling pubmed-75563622020-10-30 Hereditary Hemorrhagic Telangiectasia and Refractory Ascites Thandassery, Ragesh B. Patel, Rahul S. Grewal, Priya ACG Case Rep J Case Report Hereditary hemorrhagic telangiectasia is a rare autosomal dominant disease that can involve the liver. The presence of arteriohepatic venous shunts can lead to high output cardiac failure and biliary ischemia, whereas arterioportal venous shunts can result in portal hypertension. Cirrhosis and nodular regenerative hyperplasia are also reported in these patients. Management of these patients in the setting of symptomatic liver disease is challenging. Transarterial embolization and hepatic artery ligation are usually considered palliative options. In selected cases, orthotopic liver transplantation can cure both liver disease and heart failure. Wolters Kluwer 2020-10-14 /pmc/articles/PMC7556362/ /pubmed/33134402 http://dx.doi.org/10.14309/crj.0000000000000458 Text en © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The American College of Gastroenterology. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Case Report
Thandassery, Ragesh B.
Patel, Rahul S.
Grewal, Priya
Hereditary Hemorrhagic Telangiectasia and Refractory Ascites
title Hereditary Hemorrhagic Telangiectasia and Refractory Ascites
title_full Hereditary Hemorrhagic Telangiectasia and Refractory Ascites
title_fullStr Hereditary Hemorrhagic Telangiectasia and Refractory Ascites
title_full_unstemmed Hereditary Hemorrhagic Telangiectasia and Refractory Ascites
title_short Hereditary Hemorrhagic Telangiectasia and Refractory Ascites
title_sort hereditary hemorrhagic telangiectasia and refractory ascites
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7556362/
https://www.ncbi.nlm.nih.gov/pubmed/33134402
http://dx.doi.org/10.14309/crj.0000000000000458
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