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Superior mesenteric artery syndrome: A rare but life threatening disease

Superior mesenteric artery syndrome was observed in an adolescent patient. He had a 1-day history of nausea, vomiting, and abdominal pain, without chronic or recurrent symptoms. Diagnosis was established by abdominal plain x-ray, contrast enhanced abdominal computed tomography, and endoscopic examin...

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Autores principales: Ugras, Meltem, Bicer, Suat, Coskun, Fatma Tugba, Romano, Endi, Ekci, Baki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5459523/
https://www.ncbi.nlm.nih.gov/pubmed/28616620
http://dx.doi.org/10.1016/j.tjem.2017.01.001
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author Ugras, Meltem
Bicer, Suat
Coskun, Fatma Tugba
Romano, Endi
Ekci, Baki
author_facet Ugras, Meltem
Bicer, Suat
Coskun, Fatma Tugba
Romano, Endi
Ekci, Baki
author_sort Ugras, Meltem
collection PubMed
description Superior mesenteric artery syndrome was observed in an adolescent patient. He had a 1-day history of nausea, vomiting, and abdominal pain, without chronic or recurrent symptoms. Diagnosis was established by abdominal plain x-ray, contrast enhanced abdominal computed tomography, and endoscopic examination. The patient was hospitalized, monitorized, and decompressed by nasogastric tube without oral feeding. The symptoms of the patient were gradually relieved by conservative treatment and he was discharged after one week. Clinicians should be careful when facing upper gastrointestinal symptoms that are resistant and non-responsive to treatment, and this syndrome should be kept in mind. This case is presented to draw attention to this disease because of its rare incidence.
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spelling pubmed-54595232017-06-14 Superior mesenteric artery syndrome: A rare but life threatening disease Ugras, Meltem Bicer, Suat Coskun, Fatma Tugba Romano, Endi Ekci, Baki Turk J Emerg Med Case Report Superior mesenteric artery syndrome was observed in an adolescent patient. He had a 1-day history of nausea, vomiting, and abdominal pain, without chronic or recurrent symptoms. Diagnosis was established by abdominal plain x-ray, contrast enhanced abdominal computed tomography, and endoscopic examination. The patient was hospitalized, monitorized, and decompressed by nasogastric tube without oral feeding. The symptoms of the patient were gradually relieved by conservative treatment and he was discharged after one week. Clinicians should be careful when facing upper gastrointestinal symptoms that are resistant and non-responsive to treatment, and this syndrome should be kept in mind. This case is presented to draw attention to this disease because of its rare incidence. Elsevier 2017-01-31 /pmc/articles/PMC5459523/ /pubmed/28616620 http://dx.doi.org/10.1016/j.tjem.2017.01.001 Text en Copyright © 2017 The Emergency Medicine Association of Turkey. Production and hosting by Elsevier B.V. on behalf of the Owner. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Ugras, Meltem
Bicer, Suat
Coskun, Fatma Tugba
Romano, Endi
Ekci, Baki
Superior mesenteric artery syndrome: A rare but life threatening disease
title Superior mesenteric artery syndrome: A rare but life threatening disease
title_full Superior mesenteric artery syndrome: A rare but life threatening disease
title_fullStr Superior mesenteric artery syndrome: A rare but life threatening disease
title_full_unstemmed Superior mesenteric artery syndrome: A rare but life threatening disease
title_short Superior mesenteric artery syndrome: A rare but life threatening disease
title_sort superior mesenteric artery syndrome: a rare but life threatening disease
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5459523/
https://www.ncbi.nlm.nih.gov/pubmed/28616620
http://dx.doi.org/10.1016/j.tjem.2017.01.001
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