Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
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
_version_ 1783356828394979328
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
work_keys_str_mv AT molinaproanogabrielalejandro wilkiessyndromeamissedopportunity
AT coboandrademariamercedes wilkiessyndromeamissedopportunity
AT guadaluperodriguezramiroantonio wilkiessyndromeamissedopportunity
AT galvezsalazarpatriciofernando wilkiessyndromeamissedopportunity
AT cadenaaguirrediegopaul wilkiessyndromeamissedopportunity
AT gonzalezpomagregoriovicente wilkiessyndromeamissedopportunity
AT gutierrezgranjabernardomiguel wilkiessyndromeamissedopportunity