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Meckels diverticulum and intestinal ischaemia

We report an exceptional case of intestinal ischaemia requiring resection, secondary to torsion around a long Meckel’s diverticulum. Meckel’s diverticulum is an uncommon congenital abnormality of the small bowel. Meckel’s diverticulum giving rise to intestinal ischaemia that requires resection is ve...

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Detalles Bibliográficos
Autores principales: Halliday, J., Jamieson, RW, Gillies, TE
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JSCR Publishing Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3649195/
https://www.ncbi.nlm.nih.gov/pubmed/24950543
http://dx.doi.org/10.1093/jscr/2011.1.5
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author Halliday, J.
Jamieson, RW
Gillies, TE
author_facet Halliday, J.
Jamieson, RW
Gillies, TE
author_sort Halliday, J.
collection PubMed
description We report an exceptional case of intestinal ischaemia requiring resection, secondary to torsion around a long Meckel’s diverticulum. Meckel’s diverticulum is an uncommon congenital abnormality of the small bowel. Meckel’s diverticulum giving rise to intestinal ischaemia that requires resection is very rare but potentially fatal complication. A 62 year old woman presented as an emergency with sudden onset upper abdominal pain and vomiting. Clinical suspicion of cholecystitis prompted an ultrasound scan which revealed a distended gallbladder with multiple gallstones and an otherwise normal abdomen. Laparoscopy revealed a large volume of free blood in all four quadrants and a loop of gangrenous small bowel. The case was converted to laparotomy and a 640 mm loop of infarcted small bowel, torted around a Meckel’s diverticulum, was resected. Detection of a complication arising from a Meckel’s diverticulum presents a diagnostic challenge and can be mistaken for more common surgical presentations.
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spelling pubmed-36491952013-05-14 Meckels diverticulum and intestinal ischaemia Halliday, J. Jamieson, RW Gillies, TE J Surg Case Rep Upper GI Surgery We report an exceptional case of intestinal ischaemia requiring resection, secondary to torsion around a long Meckel’s diverticulum. Meckel’s diverticulum is an uncommon congenital abnormality of the small bowel. Meckel’s diverticulum giving rise to intestinal ischaemia that requires resection is very rare but potentially fatal complication. A 62 year old woman presented as an emergency with sudden onset upper abdominal pain and vomiting. Clinical suspicion of cholecystitis prompted an ultrasound scan which revealed a distended gallbladder with multiple gallstones and an otherwise normal abdomen. Laparoscopy revealed a large volume of free blood in all four quadrants and a loop of gangrenous small bowel. The case was converted to laparotomy and a 640 mm loop of infarcted small bowel, torted around a Meckel’s diverticulum, was resected. Detection of a complication arising from a Meckel’s diverticulum presents a diagnostic challenge and can be mistaken for more common surgical presentations. JSCR Publishing Ltd 2011-01-01 /pmc/articles/PMC3649195/ /pubmed/24950543 http://dx.doi.org/10.1093/jscr/2011.1.5 Text en © JSCR
spellingShingle Upper GI Surgery
Halliday, J.
Jamieson, RW
Gillies, TE
Meckels diverticulum and intestinal ischaemia
title Meckels diverticulum and intestinal ischaemia
title_full Meckels diverticulum and intestinal ischaemia
title_fullStr Meckels diverticulum and intestinal ischaemia
title_full_unstemmed Meckels diverticulum and intestinal ischaemia
title_short Meckels diverticulum and intestinal ischaemia
title_sort meckels diverticulum and intestinal ischaemia
topic Upper GI Surgery
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3649195/
https://www.ncbi.nlm.nih.gov/pubmed/24950543
http://dx.doi.org/10.1093/jscr/2011.1.5
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