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Salvage living donor liver transplantation after percutaneous transluminal angioplasty for recurrent Budd-Chiari syndrome: a case report

INTRODUCTION: Budd-Chiari syndrome is a very rare pathological entity that ultimately leads to liver failure. Several therapeutic modalities, including percutaneous transluminal angioplasty, have been attempted to save the life of patients with Budd-Chiari syndrome. Few reports have described a salv...

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Autores principales: Shirai, Yusaku, Yoshiji, Hitoshi, Ko, Saiho, Yamazaki, Masaharu, Ikenaka, Yasuhide, Noguchi, Ryuichi, Morioka, Chie, Kaji, Kosuke, Aihara, Yosuke, Nakanishi, Keisuke, Yamao, Junichi, Toyohara, Masahisa, Mitoro, Akira, Sawai, Masayoshi, Yoshida, Motoyuki, Fujimoto, Masao, Uemura, Masahito, Nakajima, Yoshiyuki, Fukui, Hiroshi
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3078858/
https://www.ncbi.nlm.nih.gov/pubmed/21447168
http://dx.doi.org/10.1186/1752-1947-5-124
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author Shirai, Yusaku
Yoshiji, Hitoshi
Ko, Saiho
Yamazaki, Masaharu
Ikenaka, Yasuhide
Noguchi, Ryuichi
Morioka, Chie
Kaji, Kosuke
Aihara, Yosuke
Nakanishi, Keisuke
Yamao, Junichi
Toyohara, Masahisa
Mitoro, Akira
Sawai, Masayoshi
Yoshida, Motoyuki
Fujimoto, Masao
Uemura, Masahito
Nakajima, Yoshiyuki
Fukui, Hiroshi
author_facet Shirai, Yusaku
Yoshiji, Hitoshi
Ko, Saiho
Yamazaki, Masaharu
Ikenaka, Yasuhide
Noguchi, Ryuichi
Morioka, Chie
Kaji, Kosuke
Aihara, Yosuke
Nakanishi, Keisuke
Yamao, Junichi
Toyohara, Masahisa
Mitoro, Akira
Sawai, Masayoshi
Yoshida, Motoyuki
Fujimoto, Masao
Uemura, Masahito
Nakajima, Yoshiyuki
Fukui, Hiroshi
author_sort Shirai, Yusaku
collection PubMed
description INTRODUCTION: Budd-Chiari syndrome is a very rare pathological entity that ultimately leads to liver failure. Several therapeutic modalities, including percutaneous transluminal angioplasty, have been attempted to save the life of patients with Budd-Chiari syndrome. Few reports have described a salvage living donor liver transplantation performed after percutaneous transluminal angioplasty in a patient with acute Budd-Chiari syndrome. CASE PRESENTATION: A 26-year-old Japanese man developed severe progressive manifestations, such as massive ascites and hematemesis due to rupture of esophageal varices. After making several investigations, we diagnosed the case as Budd-Chiari syndrome. We first performed percutaneous transluminal angioplasty to dilate a short-segment stenosis of his inferior vena cava. The first percutaneous transluminal angioplasty greatly improved the clinical manifestations. However, after a year, re-stenosis was detected, and a second percutaneous transluminal angioplasty failed to open the severe stricture of his inferior vena cava. Since our patient had manifestations of acute liver failure, we decided to perform salvage living donor liver transplantation from his brother. The transplantation was successfully performed and all clinical manifestations were remarkably alleviated. CONCLUSION: In cases of recurrent Budd-Chiari syndrome, the blocked hepatic venous outflow is not always relieved, even with invasive therapies. We have to take into account the possibility of adopting alternative salvage therapies if the first therapeutic modalities fail. When invasive therapy such as percutaneous transluminal angioplasty fails, liver transplantation should be considered as an alternative option.
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spelling pubmed-30788582011-04-19 Salvage living donor liver transplantation after percutaneous transluminal angioplasty for recurrent Budd-Chiari syndrome: a case report Shirai, Yusaku Yoshiji, Hitoshi Ko, Saiho Yamazaki, Masaharu Ikenaka, Yasuhide Noguchi, Ryuichi Morioka, Chie Kaji, Kosuke Aihara, Yosuke Nakanishi, Keisuke Yamao, Junichi Toyohara, Masahisa Mitoro, Akira Sawai, Masayoshi Yoshida, Motoyuki Fujimoto, Masao Uemura, Masahito Nakajima, Yoshiyuki Fukui, Hiroshi J Med Case Reports Case Report INTRODUCTION: Budd-Chiari syndrome is a very rare pathological entity that ultimately leads to liver failure. Several therapeutic modalities, including percutaneous transluminal angioplasty, have been attempted to save the life of patients with Budd-Chiari syndrome. Few reports have described a salvage living donor liver transplantation performed after percutaneous transluminal angioplasty in a patient with acute Budd-Chiari syndrome. CASE PRESENTATION: A 26-year-old Japanese man developed severe progressive manifestations, such as massive ascites and hematemesis due to rupture of esophageal varices. After making several investigations, we diagnosed the case as Budd-Chiari syndrome. We first performed percutaneous transluminal angioplasty to dilate a short-segment stenosis of his inferior vena cava. The first percutaneous transluminal angioplasty greatly improved the clinical manifestations. However, after a year, re-stenosis was detected, and a second percutaneous transluminal angioplasty failed to open the severe stricture of his inferior vena cava. Since our patient had manifestations of acute liver failure, we decided to perform salvage living donor liver transplantation from his brother. The transplantation was successfully performed and all clinical manifestations were remarkably alleviated. CONCLUSION: In cases of recurrent Budd-Chiari syndrome, the blocked hepatic venous outflow is not always relieved, even with invasive therapies. We have to take into account the possibility of adopting alternative salvage therapies if the first therapeutic modalities fail. When invasive therapy such as percutaneous transluminal angioplasty fails, liver transplantation should be considered as an alternative option. BioMed Central 2011-03-29 /pmc/articles/PMC3078858/ /pubmed/21447168 http://dx.doi.org/10.1186/1752-1947-5-124 Text en Copyright ©2011 Shirai 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 Case Report
Shirai, Yusaku
Yoshiji, Hitoshi
Ko, Saiho
Yamazaki, Masaharu
Ikenaka, Yasuhide
Noguchi, Ryuichi
Morioka, Chie
Kaji, Kosuke
Aihara, Yosuke
Nakanishi, Keisuke
Yamao, Junichi
Toyohara, Masahisa
Mitoro, Akira
Sawai, Masayoshi
Yoshida, Motoyuki
Fujimoto, Masao
Uemura, Masahito
Nakajima, Yoshiyuki
Fukui, Hiroshi
Salvage living donor liver transplantation after percutaneous transluminal angioplasty for recurrent Budd-Chiari syndrome: a case report
title Salvage living donor liver transplantation after percutaneous transluminal angioplasty for recurrent Budd-Chiari syndrome: a case report
title_full Salvage living donor liver transplantation after percutaneous transluminal angioplasty for recurrent Budd-Chiari syndrome: a case report
title_fullStr Salvage living donor liver transplantation after percutaneous transluminal angioplasty for recurrent Budd-Chiari syndrome: a case report
title_full_unstemmed Salvage living donor liver transplantation after percutaneous transluminal angioplasty for recurrent Budd-Chiari syndrome: a case report
title_short Salvage living donor liver transplantation after percutaneous transluminal angioplasty for recurrent Budd-Chiari syndrome: a case report
title_sort salvage living donor liver transplantation after percutaneous transluminal angioplasty for recurrent budd-chiari syndrome: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3078858/
https://www.ncbi.nlm.nih.gov/pubmed/21447168
http://dx.doi.org/10.1186/1752-1947-5-124
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