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Budd-Chiari Syndrome and Esophageal Achalasia: Unrecognized Intrahepatic Cholangiocarcinoma Invading Multiple Organs
Intrahepatic cholangiocarcinoma (ICC) is the second-most common primary liver cancer, although its occurrence is relatively rare. Budd-Chiari syndrome (BCS) is characterized by outflow obstruction from the liver, with hepatocellular carcinoma being the most common cause of malignant BCS. In this cas...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society of Internal Medicine
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6120825/ https://www.ncbi.nlm.nih.gov/pubmed/29526953 http://dx.doi.org/10.2169/internalmedicine.0448-17 |
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author | Kakisaka, Keisuke Endo, Kei Sugimoto, Ryo Ishida, Kazuyuki Sugai, Tamotsu Takikawa, Yasuhiro |
author_facet | Kakisaka, Keisuke Endo, Kei Sugimoto, Ryo Ishida, Kazuyuki Sugai, Tamotsu Takikawa, Yasuhiro |
author_sort | Kakisaka, Keisuke |
collection | PubMed |
description | Intrahepatic cholangiocarcinoma (ICC) is the second-most common primary liver cancer, although its occurrence is relatively rare. Budd-Chiari syndrome (BCS) is characterized by outflow obstruction from the liver, with hepatocellular carcinoma being the most common cause of malignant BCS. In this case report, we describe the occurrence of an unrecognized ICC that induced BCS and esophageal achalasia. |
format | Online Article Text |
id | pubmed-6120825 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Japanese Society of Internal Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-61208252018-09-04 Budd-Chiari Syndrome and Esophageal Achalasia: Unrecognized Intrahepatic Cholangiocarcinoma Invading Multiple Organs Kakisaka, Keisuke Endo, Kei Sugimoto, Ryo Ishida, Kazuyuki Sugai, Tamotsu Takikawa, Yasuhiro Intern Med Case Report Intrahepatic cholangiocarcinoma (ICC) is the second-most common primary liver cancer, although its occurrence is relatively rare. Budd-Chiari syndrome (BCS) is characterized by outflow obstruction from the liver, with hepatocellular carcinoma being the most common cause of malignant BCS. In this case report, we describe the occurrence of an unrecognized ICC that induced BCS and esophageal achalasia. The Japanese Society of Internal Medicine 2018-03-09 2018-08-01 /pmc/articles/PMC6120825/ /pubmed/29526953 http://dx.doi.org/10.2169/internalmedicine.0448-17 Text en Copyright © 2018 by The Japanese Society of Internal Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/ The Internal Medicine is an Open Access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Kakisaka, Keisuke Endo, Kei Sugimoto, Ryo Ishida, Kazuyuki Sugai, Tamotsu Takikawa, Yasuhiro Budd-Chiari Syndrome and Esophageal Achalasia: Unrecognized Intrahepatic Cholangiocarcinoma Invading Multiple Organs |
title | Budd-Chiari Syndrome and Esophageal Achalasia: Unrecognized Intrahepatic Cholangiocarcinoma Invading Multiple Organs |
title_full | Budd-Chiari Syndrome and Esophageal Achalasia: Unrecognized Intrahepatic Cholangiocarcinoma Invading Multiple Organs |
title_fullStr | Budd-Chiari Syndrome and Esophageal Achalasia: Unrecognized Intrahepatic Cholangiocarcinoma Invading Multiple Organs |
title_full_unstemmed | Budd-Chiari Syndrome and Esophageal Achalasia: Unrecognized Intrahepatic Cholangiocarcinoma Invading Multiple Organs |
title_short | Budd-Chiari Syndrome and Esophageal Achalasia: Unrecognized Intrahepatic Cholangiocarcinoma Invading Multiple Organs |
title_sort | budd-chiari syndrome and esophageal achalasia: unrecognized intrahepatic cholangiocarcinoma invading multiple organs |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6120825/ https://www.ncbi.nlm.nih.gov/pubmed/29526953 http://dx.doi.org/10.2169/internalmedicine.0448-17 |
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