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Food fear, quick satiety and vomiting in a 16 years old girl: It’s bulimia, or maybe not…? A case report of Wilkie’s syndrome (superior mesenteric artery syndrome)
INTRODUCTION: Wilkie’s syndrome (WS), also known as superior mesenteric artery syndrome, is a rare clinical entity caused by compression of the horizontal (third) part of the duodenum between the superior mesenteric artery and the abdominal aorta leading to duodenal obstruction. PRESENTATION OF CASE...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6854068/ https://www.ncbi.nlm.nih.gov/pubmed/31726254 http://dx.doi.org/10.1016/j.ijscr.2019.10.038 |
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author | Frongia, Giovanni Schenk, Jens-Peter Schaible, Anja Sauer, Peter Mehrabi, Arianeb Günther, Patrick |
author_facet | Frongia, Giovanni Schenk, Jens-Peter Schaible, Anja Sauer, Peter Mehrabi, Arianeb Günther, Patrick |
author_sort | Frongia, Giovanni |
collection | PubMed |
description | INTRODUCTION: Wilkie’s syndrome (WS), also known as superior mesenteric artery syndrome, is a rare clinical entity caused by compression of the horizontal (third) part of the duodenum between the superior mesenteric artery and the abdominal aorta leading to duodenal obstruction. PRESENTATION OF CASE: We report a case of a 16 years girl with long-term history of spontaneous vomiting and self-induced vomiting, also suffering from recurrent retrosternal pain, weight loss and thus reduced quality of life. Contrast intestinal series showed a large axial hernia which was laparoscopically reduced and treated by hiatoplasty and anterior hemifundoplication. After initial relief, recurrent postprandial nausea and vomiting reoccurred 4 weeks postoperatively. Abdominal MRI study revealed findings compatible with WS. After endoscopic exclusion of an anatomical duodenal lumen stenosis, she was successfully treated by duodeno-jejunostomy with a favorable outcome. DISCUSSION: WS might be hidden behind presumably more evident diagnoses such as bulimia, significant axial hernia and gastro-esophageal reflux disease in patients with recurred vomiting, abdominal pain and weight loss. CONCLUSION: The rare clinical entity of a WS necessitates a targeted diagnostic evaluation and therapy. Clinical details, diagnostic studies and treatment are discussed here. |
format | Online Article Text |
id | pubmed-6854068 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-68540682019-11-21 Food fear, quick satiety and vomiting in a 16 years old girl: It’s bulimia, or maybe not…? A case report of Wilkie’s syndrome (superior mesenteric artery syndrome) Frongia, Giovanni Schenk, Jens-Peter Schaible, Anja Sauer, Peter Mehrabi, Arianeb Günther, Patrick Int J Surg Case Rep Article INTRODUCTION: Wilkie’s syndrome (WS), also known as superior mesenteric artery syndrome, is a rare clinical entity caused by compression of the horizontal (third) part of the duodenum between the superior mesenteric artery and the abdominal aorta leading to duodenal obstruction. PRESENTATION OF CASE: We report a case of a 16 years girl with long-term history of spontaneous vomiting and self-induced vomiting, also suffering from recurrent retrosternal pain, weight loss and thus reduced quality of life. Contrast intestinal series showed a large axial hernia which was laparoscopically reduced and treated by hiatoplasty and anterior hemifundoplication. After initial relief, recurrent postprandial nausea and vomiting reoccurred 4 weeks postoperatively. Abdominal MRI study revealed findings compatible with WS. After endoscopic exclusion of an anatomical duodenal lumen stenosis, she was successfully treated by duodeno-jejunostomy with a favorable outcome. DISCUSSION: WS might be hidden behind presumably more evident diagnoses such as bulimia, significant axial hernia and gastro-esophageal reflux disease in patients with recurred vomiting, abdominal pain and weight loss. CONCLUSION: The rare clinical entity of a WS necessitates a targeted diagnostic evaluation and therapy. Clinical details, diagnostic studies and treatment are discussed here. Elsevier 2019-11-06 /pmc/articles/PMC6854068/ /pubmed/31726254 http://dx.doi.org/10.1016/j.ijscr.2019.10.038 Text en © 2019 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Frongia, Giovanni Schenk, Jens-Peter Schaible, Anja Sauer, Peter Mehrabi, Arianeb Günther, Patrick Food fear, quick satiety and vomiting in a 16 years old girl: It’s bulimia, or maybe not…? A case report of Wilkie’s syndrome (superior mesenteric artery syndrome) |
title | Food fear, quick satiety and vomiting in a 16 years old girl: It’s bulimia, or maybe not…? A case report of Wilkie’s syndrome (superior mesenteric artery syndrome) |
title_full | Food fear, quick satiety and vomiting in a 16 years old girl: It’s bulimia, or maybe not…? A case report of Wilkie’s syndrome (superior mesenteric artery syndrome) |
title_fullStr | Food fear, quick satiety and vomiting in a 16 years old girl: It’s bulimia, or maybe not…? A case report of Wilkie’s syndrome (superior mesenteric artery syndrome) |
title_full_unstemmed | Food fear, quick satiety and vomiting in a 16 years old girl: It’s bulimia, or maybe not…? A case report of Wilkie’s syndrome (superior mesenteric artery syndrome) |
title_short | Food fear, quick satiety and vomiting in a 16 years old girl: It’s bulimia, or maybe not…? A case report of Wilkie’s syndrome (superior mesenteric artery syndrome) |
title_sort | food fear, quick satiety and vomiting in a 16 years old girl: it’s bulimia, or maybe not…? a case report of wilkie’s syndrome (superior mesenteric artery syndrome) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6854068/ https://www.ncbi.nlm.nih.gov/pubmed/31726254 http://dx.doi.org/10.1016/j.ijscr.2019.10.038 |
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