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Rare spontaneous intrahepatic portosystemic shunt in hepatitis B-induced cirrhosis: A case report
BACKGROUND: The portosystemic shunt is the pathway between the portal vein (PV) and systemic circulation. A spontaneous intrahepatic portosystemic shunt (SPISS) is a rare portosystemic shunt type. Here we report an extremely rare type of SPISS, a spontaneous intrahepatic PV-inferior vena cava shunt...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Baishideng Publishing Group Inc
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745322/ https://www.ncbi.nlm.nih.gov/pubmed/31559295 http://dx.doi.org/10.12998/wjcc.v7.i17.2573 |
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author | Tan, You-Wen Sheng, Jian-Hui Tan, Hui-Ying Sun, Li Yin, Yu-Mei |
author_facet | Tan, You-Wen Sheng, Jian-Hui Tan, Hui-Ying Sun, Li Yin, Yu-Mei |
author_sort | Tan, You-Wen |
collection | PubMed |
description | BACKGROUND: The portosystemic shunt is the pathway between the portal vein (PV) and systemic circulation. A spontaneous intrahepatic portosystemic shunt (SPISS) is a rare portosystemic shunt type. Here we report an extremely rare type of SPISS, a spontaneous intrahepatic PV-inferior vena cava shunt (SPIVCS). CASE SUMMARY: A 66-year-old woman was admitted to our hospital with the complaint of abdominal distention and a decreased appetite for 1 mo. The patient had a 20-year history of hepatitis B surface antigen positivity and a 5-year history of cirrhosis. She had been treated with Chinese herbal medicine for a long time. Liver function tests showed: alanine aminotransferase, 35 U/L; aspartate aminotransferase, 42 U/L; serum albumin (ALB) 32.2 g/L; and serum ascites ALB gradient, 25.2 g/L. Abdominal ultrasonography and enhanced computed tomography showed that the left branch of the PV was thin and occluded; the right branch of the PV was thick and showed a vermicular dilatation vein cluster in the upper pole of the right kidney that branched out and converged into the inferior vena cava from the bare area of the lower right posterior lobe of the liver. We diagnosed her with an extremely rare SPIVCS caused by portal hypertension and provided symptomatic treatment after admission. One week later, her symptoms disappeared and she was discharged. CONCLUSION: SPIVCS is a rare portosystemic shunt with a clear history of cirrhosis and portal hypertension. Clarifying the type PV shunt has important clinical significance. |
format | Online Article Text |
id | pubmed-6745322 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-67453222019-09-26 Rare spontaneous intrahepatic portosystemic shunt in hepatitis B-induced cirrhosis: A case report Tan, You-Wen Sheng, Jian-Hui Tan, Hui-Ying Sun, Li Yin, Yu-Mei World J Clin Cases Case Report BACKGROUND: The portosystemic shunt is the pathway between the portal vein (PV) and systemic circulation. A spontaneous intrahepatic portosystemic shunt (SPISS) is a rare portosystemic shunt type. Here we report an extremely rare type of SPISS, a spontaneous intrahepatic PV-inferior vena cava shunt (SPIVCS). CASE SUMMARY: A 66-year-old woman was admitted to our hospital with the complaint of abdominal distention and a decreased appetite for 1 mo. The patient had a 20-year history of hepatitis B surface antigen positivity and a 5-year history of cirrhosis. She had been treated with Chinese herbal medicine for a long time. Liver function tests showed: alanine aminotransferase, 35 U/L; aspartate aminotransferase, 42 U/L; serum albumin (ALB) 32.2 g/L; and serum ascites ALB gradient, 25.2 g/L. Abdominal ultrasonography and enhanced computed tomography showed that the left branch of the PV was thin and occluded; the right branch of the PV was thick and showed a vermicular dilatation vein cluster in the upper pole of the right kidney that branched out and converged into the inferior vena cava from the bare area of the lower right posterior lobe of the liver. We diagnosed her with an extremely rare SPIVCS caused by portal hypertension and provided symptomatic treatment after admission. One week later, her symptoms disappeared and she was discharged. CONCLUSION: SPIVCS is a rare portosystemic shunt with a clear history of cirrhosis and portal hypertension. Clarifying the type PV shunt has important clinical significance. Baishideng Publishing Group Inc 2019-09-06 2019-09-06 /pmc/articles/PMC6745322/ /pubmed/31559295 http://dx.doi.org/10.12998/wjcc.v7.i17.2573 Text en ©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Case Report Tan, You-Wen Sheng, Jian-Hui Tan, Hui-Ying Sun, Li Yin, Yu-Mei Rare spontaneous intrahepatic portosystemic shunt in hepatitis B-induced cirrhosis: A case report |
title | Rare spontaneous intrahepatic portosystemic shunt in hepatitis B-induced cirrhosis: A case report |
title_full | Rare spontaneous intrahepatic portosystemic shunt in hepatitis B-induced cirrhosis: A case report |
title_fullStr | Rare spontaneous intrahepatic portosystemic shunt in hepatitis B-induced cirrhosis: A case report |
title_full_unstemmed | Rare spontaneous intrahepatic portosystemic shunt in hepatitis B-induced cirrhosis: A case report |
title_short | Rare spontaneous intrahepatic portosystemic shunt in hepatitis B-induced cirrhosis: A case report |
title_sort | rare spontaneous intrahepatic portosystemic shunt in hepatitis b-induced cirrhosis: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745322/ https://www.ncbi.nlm.nih.gov/pubmed/31559295 http://dx.doi.org/10.12998/wjcc.v7.i17.2573 |
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