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A Unique Case of Hematemesis in a 17-Year-Old Female

Hemosuccus pancreaticus (HP) is a rare cause of gastrointestinal bleeding (GIB) that should be considered in a patient with a history of pancreatitis and GIB. A 17-year-old female presented with nausea followed by an episode of hematemesis. Fourteen weeks prior to presentation, she had 3 episodes of...

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Autores principales: Zuchelli, Tobias, Alsheik, Eva, Bhandari, Bhavik, Ringold, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American College of Gastroenterology 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4435304/
https://www.ncbi.nlm.nih.gov/pubmed/26157858
http://dx.doi.org/10.14309/crj.2014.34
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author Zuchelli, Tobias
Alsheik, Eva
Bhandari, Bhavik
Ringold, Daniel
author_facet Zuchelli, Tobias
Alsheik, Eva
Bhandari, Bhavik
Ringold, Daniel
author_sort Zuchelli, Tobias
collection PubMed
description Hemosuccus pancreaticus (HP) is a rare cause of gastrointestinal bleeding (GIB) that should be considered in a patient with a history of pancreatitis and GIB. A 17-year-old female presented with nausea followed by an episode of hematemesis. Fourteen weeks prior to presentation, she had 3 episodes of vomiting within a week. Six weeks prior to presentation, she developed abdominal pain and was diagnosed with acute idiopathic pancreatitis. Computed tomography (CT) revealed a cystic lesion arising in the gastroduodenal artery (GDA), and coil embolization was performed. There are no reported cases of HP in an adolescent with acute idiopathic pancreatitis.
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spelling pubmed-44353042015-07-08 A Unique Case of Hematemesis in a 17-Year-Old Female Zuchelli, Tobias Alsheik, Eva Bhandari, Bhavik Ringold, Daniel ACG Case Rep J Case Report Hemosuccus pancreaticus (HP) is a rare cause of gastrointestinal bleeding (GIB) that should be considered in a patient with a history of pancreatitis and GIB. A 17-year-old female presented with nausea followed by an episode of hematemesis. Fourteen weeks prior to presentation, she had 3 episodes of vomiting within a week. Six weeks prior to presentation, she developed abdominal pain and was diagnosed with acute idiopathic pancreatitis. Computed tomography (CT) revealed a cystic lesion arising in the gastroduodenal artery (GDA), and coil embolization was performed. There are no reported cases of HP in an adolescent with acute idiopathic pancreatitis. American College of Gastroenterology 2014-04-04 /pmc/articles/PMC4435304/ /pubmed/26157858 http://dx.doi.org/10.14309/crj.2014.34 Text en Copyright © Zuchelli et al. This is an open-access article. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Case Report
Zuchelli, Tobias
Alsheik, Eva
Bhandari, Bhavik
Ringold, Daniel
A Unique Case of Hematemesis in a 17-Year-Old Female
title A Unique Case of Hematemesis in a 17-Year-Old Female
title_full A Unique Case of Hematemesis in a 17-Year-Old Female
title_fullStr A Unique Case of Hematemesis in a 17-Year-Old Female
title_full_unstemmed A Unique Case of Hematemesis in a 17-Year-Old Female
title_short A Unique Case of Hematemesis in a 17-Year-Old Female
title_sort unique case of hematemesis in a 17-year-old female
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4435304/
https://www.ncbi.nlm.nih.gov/pubmed/26157858
http://dx.doi.org/10.14309/crj.2014.34
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