DOUBLE MECKEL'S DIVERTICULUM PRESENTING AS ACUTE APPENDICITIS: A CASE

Background: Meckel's diverticulum is the most common developmental anomaly of the gastrointestinal tract, affecting 1-3% of the general population. This anomaly is caused by incomplete obliteration of the omphalomesenteric duct during the 7th week of gestation and is located in the last meter o...

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Main Authors: Emre, A, Akbulut, S, Yilmaz, M, Kanlioz, M, Aydin, BE
Language:unknown
Published: 2013
Subjects:
Online Access:http://hdl.handle.net/11616/27931
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spelling ftinonuuniv:oai:abakus.inonu.edu.tr:11616/27931 2023-05-15T18:12:46+02:00 DOUBLE MECKEL'S DIVERTICULUM PRESENTING AS ACUTE APPENDICITIS: A CASE Emre, A Akbulut, S Yilmaz, M Kanlioz, M Aydin, BE 2013 http://hdl.handle.net/11616/27931 unknown http://hdl.handle.net/11616/27931 JOURNAL OF EMERGENCY MEDICINE 2013 ftinonuuniv 2022-03-28T19:51:04Z Background: Meckel's diverticulum is the most common developmental anomaly of the gastrointestinal tract, affecting 1-3% of the general population. This anomaly is caused by incomplete obliteration of the omphalomesenteric duct during the 7th week of gestation and is located in the last meter of the ileum in 90% of patients. Meckel's diverticulumis often an incidental finding during a laparotomy for other causes, such as acute appendicitis, and occasional complications are bleeding, obstruction, diverticulitis, and perforation. Objective: Primary aim of this study was to present and share an extremely rare case of double Meckel's diverticulum. Methods: A 20-year-old woman who was admitted due to symptoms of right lower quadrant pain, nausea, and vomiting. A laparotomy with a McBurney's incision was performed because of a presumed diagnosis of acute appendicitis. The surgical exploration revealed a double Meckel's diverticulum localized 50 cm proximal to the ileocecal valve, but no acute appendicitis. The operation was finished after a diverticulectomy and appendectomy. No complications occurred during the postoperative follow-up. Conclusions: We conducted a literature review of studies published in the English language on double Meckel's diverticulum, accessed via PubMed, Medline, and the Google Scholar databases. We found only five case reports of such a Meckel's diverticulum variant. (C) 2013 Elsevier Inc. C1 [Emre, Arif; Kanlioz, Murat] Malatya State Hosp, Dept Surg, Malatya, Turkey. [Akbulut, Sami; Yilmaz, Mehmet] Inonu Univ, Fac Med, Dept Surg, Div Liver Transplantat, TR-44280 Malatya, Turkey. [Aydin, Burcu Elif] Malatya State Hosp, Dept Pathol, Malatya, Turkey. Other/Unknown Material sami Unknown
institution Open Polar
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op_collection_id ftinonuuniv
language unknown
description Background: Meckel's diverticulum is the most common developmental anomaly of the gastrointestinal tract, affecting 1-3% of the general population. This anomaly is caused by incomplete obliteration of the omphalomesenteric duct during the 7th week of gestation and is located in the last meter of the ileum in 90% of patients. Meckel's diverticulumis often an incidental finding during a laparotomy for other causes, such as acute appendicitis, and occasional complications are bleeding, obstruction, diverticulitis, and perforation. Objective: Primary aim of this study was to present and share an extremely rare case of double Meckel's diverticulum. Methods: A 20-year-old woman who was admitted due to symptoms of right lower quadrant pain, nausea, and vomiting. A laparotomy with a McBurney's incision was performed because of a presumed diagnosis of acute appendicitis. The surgical exploration revealed a double Meckel's diverticulum localized 50 cm proximal to the ileocecal valve, but no acute appendicitis. The operation was finished after a diverticulectomy and appendectomy. No complications occurred during the postoperative follow-up. Conclusions: We conducted a literature review of studies published in the English language on double Meckel's diverticulum, accessed via PubMed, Medline, and the Google Scholar databases. We found only five case reports of such a Meckel's diverticulum variant. (C) 2013 Elsevier Inc. C1 [Emre, Arif; Kanlioz, Murat] Malatya State Hosp, Dept Surg, Malatya, Turkey. [Akbulut, Sami; Yilmaz, Mehmet] Inonu Univ, Fac Med, Dept Surg, Div Liver Transplantat, TR-44280 Malatya, Turkey. [Aydin, Burcu Elif] Malatya State Hosp, Dept Pathol, Malatya, Turkey.
author Emre, A
Akbulut, S
Yilmaz, M
Kanlioz, M
Aydin, BE
spellingShingle Emre, A
Akbulut, S
Yilmaz, M
Kanlioz, M
Aydin, BE
DOUBLE MECKEL'S DIVERTICULUM PRESENTING AS ACUTE APPENDICITIS: A CASE
author_facet Emre, A
Akbulut, S
Yilmaz, M
Kanlioz, M
Aydin, BE
author_sort Emre, A
title DOUBLE MECKEL'S DIVERTICULUM PRESENTING AS ACUTE APPENDICITIS: A CASE
title_short DOUBLE MECKEL'S DIVERTICULUM PRESENTING AS ACUTE APPENDICITIS: A CASE
title_full DOUBLE MECKEL'S DIVERTICULUM PRESENTING AS ACUTE APPENDICITIS: A CASE
title_fullStr DOUBLE MECKEL'S DIVERTICULUM PRESENTING AS ACUTE APPENDICITIS: A CASE
title_full_unstemmed DOUBLE MECKEL'S DIVERTICULUM PRESENTING AS ACUTE APPENDICITIS: A CASE
title_sort double meckel's diverticulum presenting as acute appendicitis: a case
publishDate 2013
url http://hdl.handle.net/11616/27931
genre sami
genre_facet sami
op_source JOURNAL OF EMERGENCY MEDICINE
op_relation http://hdl.handle.net/11616/27931
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