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Wilkie’s syndrome, a missed opportunity
Wilkie’s syndrome is a rare cause of duodenal obstruction that can easily be missed at clinical practice. It is characterized by nausea, abdominal pain and vomit. It usually affects young adults, and it’s caused by a low aortomesenteric angle resulting in vascular compression of the duodenum. Sympto...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149230/ https://www.ncbi.nlm.nih.gov/pubmed/30254733 http://dx.doi.org/10.1093/jscr/rjy246 |
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author | Molina Proaño, Gabriel Alejandro Cobo Andrade, María Mercedes Guadalupe Rodríguez, Ramiro Antonio Gálvez Salazar, Patricio Fernando Cadena Aguirre, Diego Paul González Poma, Gregorio Vicente Gutierrez Granja, Bernardo Miguel |
author_facet | Molina Proaño, Gabriel Alejandro Cobo Andrade, María Mercedes Guadalupe Rodríguez, Ramiro Antonio Gálvez Salazar, Patricio Fernando Cadena Aguirre, Diego Paul González Poma, Gregorio Vicente Gutierrez Granja, Bernardo Miguel |
author_sort | Molina Proaño, Gabriel Alejandro |
collection | PubMed |
description | Wilkie’s syndrome is a rare cause of duodenal obstruction that can easily be missed at clinical practice. It is characterized by nausea, abdominal pain and vomit. It usually affects young adults, and it’s caused by a low aortomesenteric angle resulting in vascular compression of the duodenum. Symptoms could resemble many of the symptoms presented in a patient with a suspected eating disorder. The non-specificity of the clinical signs and symptoms can confuse, delay the diagnosis and expose the patient to potentially hazardous therapies. We report a case of a 20-year-old patient who presented to the emergency room with a history of intermittent vomiting and abdominal pain. He had been previously misdiagnosed with an eating disorder and received physiological therapy. Nonetheless, his pain persisted. After further evaluation with the use of imaging techniques, a low aortomesenteric angle was discovered. He underwent surgery and completely recovered. On follow up controls patient is well and he no longer had episodes of vomiting. |
format | Online Article Text |
id | pubmed-6149230 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61492302018-09-25 Wilkie’s syndrome, a missed opportunity Molina Proaño, Gabriel Alejandro Cobo Andrade, María Mercedes Guadalupe Rodríguez, Ramiro Antonio Gálvez Salazar, Patricio Fernando Cadena Aguirre, Diego Paul González Poma, Gregorio Vicente Gutierrez Granja, Bernardo Miguel J Surg Case Rep Case Report Wilkie’s syndrome is a rare cause of duodenal obstruction that can easily be missed at clinical practice. It is characterized by nausea, abdominal pain and vomit. It usually affects young adults, and it’s caused by a low aortomesenteric angle resulting in vascular compression of the duodenum. Symptoms could resemble many of the symptoms presented in a patient with a suspected eating disorder. The non-specificity of the clinical signs and symptoms can confuse, delay the diagnosis and expose the patient to potentially hazardous therapies. We report a case of a 20-year-old patient who presented to the emergency room with a history of intermittent vomiting and abdominal pain. He had been previously misdiagnosed with an eating disorder and received physiological therapy. Nonetheless, his pain persisted. After further evaluation with the use of imaging techniques, a low aortomesenteric angle was discovered. He underwent surgery and completely recovered. On follow up controls patient is well and he no longer had episodes of vomiting. Oxford University Press 2018-09-21 /pmc/articles/PMC6149230/ /pubmed/30254733 http://dx.doi.org/10.1093/jscr/rjy246 Text en Published by Oxford University Press and JSCR Publishing Ltd. All rights reserved. © The Author(s) 2018. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Case Report Molina Proaño, Gabriel Alejandro Cobo Andrade, María Mercedes Guadalupe Rodríguez, Ramiro Antonio Gálvez Salazar, Patricio Fernando Cadena Aguirre, Diego Paul González Poma, Gregorio Vicente Gutierrez Granja, Bernardo Miguel Wilkie’s syndrome, a missed opportunity |
title | Wilkie’s syndrome, a missed opportunity |
title_full | Wilkie’s syndrome, a missed opportunity |
title_fullStr | Wilkie’s syndrome, a missed opportunity |
title_full_unstemmed | Wilkie’s syndrome, a missed opportunity |
title_short | Wilkie’s syndrome, a missed opportunity |
title_sort | wilkie’s syndrome, a missed opportunity |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149230/ https://www.ncbi.nlm.nih.gov/pubmed/30254733 http://dx.doi.org/10.1093/jscr/rjy246 |
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