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Portal Hypertensive Biliopathy Presents with Massive Bleeding during ERCP after Balloon Sphincteroplasty in a Noncirrhotic Saudi Sickler Patient

Portal hypertensive biliopathy (PHB) is described as abnormalities of the walls of the biliary tree secondary to portal hypertension. Gastrointestinal bleeding caused by PHB is rare. PHB as a cause of serious bleeding after sphincteroplasty during ERCP is extremely rare. Here, we report a case of PH...

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Autores principales: Al-Akwaa, Ahmad M., Elsadig, Mohammed, Al-Fayaa, Ahmed E., Al-Shehri, Mohja D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5446870/
https://www.ncbi.nlm.nih.gov/pubmed/28588619
http://dx.doi.org/10.1155/2017/4163919
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author Al-Akwaa, Ahmad M.
Elsadig, Mohammed
Al-Fayaa, Ahmed E.
Al-Shehri, Mohja D.
author_facet Al-Akwaa, Ahmad M.
Elsadig, Mohammed
Al-Fayaa, Ahmed E.
Al-Shehri, Mohja D.
author_sort Al-Akwaa, Ahmad M.
collection PubMed
description Portal hypertensive biliopathy (PHB) is described as abnormalities of the walls of the biliary tree secondary to portal hypertension. Gastrointestinal bleeding caused by PHB is rare. PHB as a cause of serious bleeding after sphincteroplasty during ERCP is extremely rare. Here, we report a case of PHB in a young Saudi male with cell sickle anemia who developed massive hemorrhage during ERCP after balloon dilation of the ampulla of Vater. We further discussed the diagnosis and management. To the best of our knowledge, no such case has been reported.
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spelling pubmed-54468702017-06-06 Portal Hypertensive Biliopathy Presents with Massive Bleeding during ERCP after Balloon Sphincteroplasty in a Noncirrhotic Saudi Sickler Patient Al-Akwaa, Ahmad M. Elsadig, Mohammed Al-Fayaa, Ahmed E. Al-Shehri, Mohja D. Case Rep Med Case Report Portal hypertensive biliopathy (PHB) is described as abnormalities of the walls of the biliary tree secondary to portal hypertension. Gastrointestinal bleeding caused by PHB is rare. PHB as a cause of serious bleeding after sphincteroplasty during ERCP is extremely rare. Here, we report a case of PHB in a young Saudi male with cell sickle anemia who developed massive hemorrhage during ERCP after balloon dilation of the ampulla of Vater. We further discussed the diagnosis and management. To the best of our knowledge, no such case has been reported. Hindawi 2017 2017-05-14 /pmc/articles/PMC5446870/ /pubmed/28588619 http://dx.doi.org/10.1155/2017/4163919 Text en Copyright © 2017 Ahmad M. Al-Akwaa et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Al-Akwaa, Ahmad M.
Elsadig, Mohammed
Al-Fayaa, Ahmed E.
Al-Shehri, Mohja D.
Portal Hypertensive Biliopathy Presents with Massive Bleeding during ERCP after Balloon Sphincteroplasty in a Noncirrhotic Saudi Sickler Patient
title Portal Hypertensive Biliopathy Presents with Massive Bleeding during ERCP after Balloon Sphincteroplasty in a Noncirrhotic Saudi Sickler Patient
title_full Portal Hypertensive Biliopathy Presents with Massive Bleeding during ERCP after Balloon Sphincteroplasty in a Noncirrhotic Saudi Sickler Patient
title_fullStr Portal Hypertensive Biliopathy Presents with Massive Bleeding during ERCP after Balloon Sphincteroplasty in a Noncirrhotic Saudi Sickler Patient
title_full_unstemmed Portal Hypertensive Biliopathy Presents with Massive Bleeding during ERCP after Balloon Sphincteroplasty in a Noncirrhotic Saudi Sickler Patient
title_short Portal Hypertensive Biliopathy Presents with Massive Bleeding during ERCP after Balloon Sphincteroplasty in a Noncirrhotic Saudi Sickler Patient
title_sort portal hypertensive biliopathy presents with massive bleeding during ercp after balloon sphincteroplasty in a noncirrhotic saudi sickler patient
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5446870/
https://www.ncbi.nlm.nih.gov/pubmed/28588619
http://dx.doi.org/10.1155/2017/4163919
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