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Clinical characteristics of hepatic Arterioportal shunts associated with hepatocellular carcinoma

BACKGROUND: Hepatic arterioportal shunt (A-P shunt) is defined as the direct blood flow established between hepatic artery and portal venous system; it is frequently observed in patients with hepatocellular carcinoma (HCC). Clinically, it is important to diagnose HCC associated A-P shunts, as it may...

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Autores principales: Wu, Huiyong, Zhao, Wei, Zhang, Jianbo, Han, Jianjun, Liu, Shuguang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6233279/
https://www.ncbi.nlm.nih.gov/pubmed/30419830
http://dx.doi.org/10.1186/s12876-018-0899-3
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author Wu, Huiyong
Zhao, Wei
Zhang, Jianbo
Han, Jianjun
Liu, Shuguang
author_facet Wu, Huiyong
Zhao, Wei
Zhang, Jianbo
Han, Jianjun
Liu, Shuguang
author_sort Wu, Huiyong
collection PubMed
description BACKGROUND: Hepatic arterioportal shunt (A-P shunt) is defined as the direct blood flow established between hepatic artery and portal venous system; it is frequently observed in patients with hepatocellular carcinoma (HCC). Clinically, it is important to diagnose HCC associated A-P shunts, as it may impact the treatment strategy of the patients. In the present study, we described the imaging findings of the HCC associated A-P shunts and discussed the treatments strategy of such patients. From the findings, we also discussed the potential cause of A-P shunts. METHODS: Clinical data of HCC patients (n = 560), admitted to the hospital between April 2012 to April 2014, were reviewed. Hepatic angiography was used to examine the presence of A-P shunts. Of the 137 patients with A-P shunts, grading of the A-P shunts was performed, and statistical analysis of the different grades of A-P shunts and clinical characteristics was performed. RESULTS: The hepatic angiography confirmed that 99 patients had typical A-P shunts (Grade 1–3), and 38 patients had atypical A-P shunts. Embolization was the main strategy used to treat A-P shunts, in which liquid embolic agents appeared to provide a better treatment outcome. The correlation analysis showed that the grading of portal vein tumor thrombus was significantly associated with the grading of A-P shunt (p = < 0.001, Spearman correlation coefficient was 0.816 ± 0.043). CONCLUSIONS: We characterized A-P shunts and proposed treatment strategy for treating HCC patients with various levels of A-P shunts. The findings supported the hypothesis that the formation of HCC associated A-P shunts was caused by tumor thrombus.
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spelling pubmed-62332792018-11-20 Clinical characteristics of hepatic Arterioportal shunts associated with hepatocellular carcinoma Wu, Huiyong Zhao, Wei Zhang, Jianbo Han, Jianjun Liu, Shuguang BMC Gastroenterol Research Article BACKGROUND: Hepatic arterioportal shunt (A-P shunt) is defined as the direct blood flow established between hepatic artery and portal venous system; it is frequently observed in patients with hepatocellular carcinoma (HCC). Clinically, it is important to diagnose HCC associated A-P shunts, as it may impact the treatment strategy of the patients. In the present study, we described the imaging findings of the HCC associated A-P shunts and discussed the treatments strategy of such patients. From the findings, we also discussed the potential cause of A-P shunts. METHODS: Clinical data of HCC patients (n = 560), admitted to the hospital between April 2012 to April 2014, were reviewed. Hepatic angiography was used to examine the presence of A-P shunts. Of the 137 patients with A-P shunts, grading of the A-P shunts was performed, and statistical analysis of the different grades of A-P shunts and clinical characteristics was performed. RESULTS: The hepatic angiography confirmed that 99 patients had typical A-P shunts (Grade 1–3), and 38 patients had atypical A-P shunts. Embolization was the main strategy used to treat A-P shunts, in which liquid embolic agents appeared to provide a better treatment outcome. The correlation analysis showed that the grading of portal vein tumor thrombus was significantly associated with the grading of A-P shunt (p = < 0.001, Spearman correlation coefficient was 0.816 ± 0.043). CONCLUSIONS: We characterized A-P shunts and proposed treatment strategy for treating HCC patients with various levels of A-P shunts. The findings supported the hypothesis that the formation of HCC associated A-P shunts was caused by tumor thrombus. BioMed Central 2018-11-12 /pmc/articles/PMC6233279/ /pubmed/30419830 http://dx.doi.org/10.1186/s12876-018-0899-3 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Wu, Huiyong
Zhao, Wei
Zhang, Jianbo
Han, Jianjun
Liu, Shuguang
Clinical characteristics of hepatic Arterioportal shunts associated with hepatocellular carcinoma
title Clinical characteristics of hepatic Arterioportal shunts associated with hepatocellular carcinoma
title_full Clinical characteristics of hepatic Arterioportal shunts associated with hepatocellular carcinoma
title_fullStr Clinical characteristics of hepatic Arterioportal shunts associated with hepatocellular carcinoma
title_full_unstemmed Clinical characteristics of hepatic Arterioportal shunts associated with hepatocellular carcinoma
title_short Clinical characteristics of hepatic Arterioportal shunts associated with hepatocellular carcinoma
title_sort clinical characteristics of hepatic arterioportal shunts associated with hepatocellular carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6233279/
https://www.ncbi.nlm.nih.gov/pubmed/30419830
http://dx.doi.org/10.1186/s12876-018-0899-3
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