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Ex vivo hepatic venography for hepatocellular carcinoma in livers explanted for liver transplantation

BACKGROUND: Hepatocellular carcinoma (HCC) is supposed to have a venous drainage system to a portal vein, which makes intrahepatic metastasis possible. However, the mechanism of extrahepatic recurrence, including the possibility of a direct route to the systemic circulation from the HCC nodules, rem...

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Autores principales: Miyazaki, Kensuke, Soyama, Akihiko, Hidaka, Masaaki, Hamasaki, Koji, Yamanouchi, Kosho, Takatsuki, Mitsuhisa, Kanematsu, Takashi, Eguchi, Susumu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3204254/
https://www.ncbi.nlm.nih.gov/pubmed/21951398
http://dx.doi.org/10.1186/1477-7819-9-111
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author Miyazaki, Kensuke
Soyama, Akihiko
Hidaka, Masaaki
Hamasaki, Koji
Yamanouchi, Kosho
Takatsuki, Mitsuhisa
Kanematsu, Takashi
Eguchi, Susumu
author_facet Miyazaki, Kensuke
Soyama, Akihiko
Hidaka, Masaaki
Hamasaki, Koji
Yamanouchi, Kosho
Takatsuki, Mitsuhisa
Kanematsu, Takashi
Eguchi, Susumu
author_sort Miyazaki, Kensuke
collection PubMed
description BACKGROUND: Hepatocellular carcinoma (HCC) is supposed to have a venous drainage system to a portal vein, which makes intrahepatic metastasis possible. However, the mechanism of extrahepatic recurrence, including the possibility of a direct route to the systemic circulation from the HCC nodules, remains unclear. Therefore, we performed retrograde hepatic venography for HCC in livers that had been explanted for liver transplantation in order to explore the possible direct connection between the hepatic vein and HCC nodules. METHODS: Of 105 living-donor liver transplantations (LDLT) performed up to July, 2009 at the Department of Surgery, Nagasaki University Hospital, dynamic hepatic venography was performed with contrast media under fluoroscopy for the most recent 13 cases with HCC. The presence of a tumor stain for each HCC case was evaluated and compared with the histological findings of HCC. RESULTS: Hepatic venography revealed a tumor stain in 2 of 13 cases (15%). Neither showed any microscopic tumor invasion of HCC into the hepatic vein. In the other 11 cases, there were 4 microscopic portal venous invasions and 2 microscopic hepatic venous invasions. No patients have shown HCC recurrence in follow-up (median period, 13 months). CONCLUSION: Using ex vivo hepatic venography, a direct connection to the hepatic vein from HCC in whole liver was revealed in 2 cases without demonstrated histopathological invasion to hepatic vein for the first time in the literature. The finding suggests that there is direct spillage of HCC cells into the systemic circulation via hepatic vein.
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spelling pubmed-32042542011-10-30 Ex vivo hepatic venography for hepatocellular carcinoma in livers explanted for liver transplantation Miyazaki, Kensuke Soyama, Akihiko Hidaka, Masaaki Hamasaki, Koji Yamanouchi, Kosho Takatsuki, Mitsuhisa Kanematsu, Takashi Eguchi, Susumu World J Surg Oncol Research BACKGROUND: Hepatocellular carcinoma (HCC) is supposed to have a venous drainage system to a portal vein, which makes intrahepatic metastasis possible. However, the mechanism of extrahepatic recurrence, including the possibility of a direct route to the systemic circulation from the HCC nodules, remains unclear. Therefore, we performed retrograde hepatic venography for HCC in livers that had been explanted for liver transplantation in order to explore the possible direct connection between the hepatic vein and HCC nodules. METHODS: Of 105 living-donor liver transplantations (LDLT) performed up to July, 2009 at the Department of Surgery, Nagasaki University Hospital, dynamic hepatic venography was performed with contrast media under fluoroscopy for the most recent 13 cases with HCC. The presence of a tumor stain for each HCC case was evaluated and compared with the histological findings of HCC. RESULTS: Hepatic venography revealed a tumor stain in 2 of 13 cases (15%). Neither showed any microscopic tumor invasion of HCC into the hepatic vein. In the other 11 cases, there were 4 microscopic portal venous invasions and 2 microscopic hepatic venous invasions. No patients have shown HCC recurrence in follow-up (median period, 13 months). CONCLUSION: Using ex vivo hepatic venography, a direct connection to the hepatic vein from HCC in whole liver was revealed in 2 cases without demonstrated histopathological invasion to hepatic vein for the first time in the literature. The finding suggests that there is direct spillage of HCC cells into the systemic circulation via hepatic vein. BioMed Central 2011-09-27 /pmc/articles/PMC3204254/ /pubmed/21951398 http://dx.doi.org/10.1186/1477-7819-9-111 Text en Copyright ©2011 Miyazaki et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Miyazaki, Kensuke
Soyama, Akihiko
Hidaka, Masaaki
Hamasaki, Koji
Yamanouchi, Kosho
Takatsuki, Mitsuhisa
Kanematsu, Takashi
Eguchi, Susumu
Ex vivo hepatic venography for hepatocellular carcinoma in livers explanted for liver transplantation
title Ex vivo hepatic venography for hepatocellular carcinoma in livers explanted for liver transplantation
title_full Ex vivo hepatic venography for hepatocellular carcinoma in livers explanted for liver transplantation
title_fullStr Ex vivo hepatic venography for hepatocellular carcinoma in livers explanted for liver transplantation
title_full_unstemmed Ex vivo hepatic venography for hepatocellular carcinoma in livers explanted for liver transplantation
title_short Ex vivo hepatic venography for hepatocellular carcinoma in livers explanted for liver transplantation
title_sort ex vivo hepatic venography for hepatocellular carcinoma in livers explanted for liver transplantation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3204254/
https://www.ncbi.nlm.nih.gov/pubmed/21951398
http://dx.doi.org/10.1186/1477-7819-9-111
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