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An unusual presentation of intestinal duplication mimicking torsion of Meckel’s diverticulum: a rare report of a pediatric case
BACKGROUND: Enteric duplication is a congenital disease that occurs throughout the entire gastrointestinal tract. Although it may sometimes cause intestinal volvulus, a few reports have described cases of enteric duplication twisted on itself. We experienced a rare pediatric case of long-segment tub...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8960505/ https://www.ncbi.nlm.nih.gov/pubmed/35344094 http://dx.doi.org/10.1186/s40792-022-01409-6 |
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author | Matsukubo, Makoto Muto, Mitsuru Kedoin, Chihiro Matsui, Mayu Murakami, Masakazu Sugita, Koshiro Yano, Keisuke Onishi, Shun Harumatsu, Toshio Yamada, Koji Yamada, Waka Kaji, Tatsuru Ieiri, Satoshi |
author_facet | Matsukubo, Makoto Muto, Mitsuru Kedoin, Chihiro Matsui, Mayu Murakami, Masakazu Sugita, Koshiro Yano, Keisuke Onishi, Shun Harumatsu, Toshio Yamada, Koji Yamada, Waka Kaji, Tatsuru Ieiri, Satoshi |
author_sort | Matsukubo, Makoto |
collection | PubMed |
description | BACKGROUND: Enteric duplication is a congenital disease that occurs throughout the entire gastrointestinal tract. Although it may sometimes cause intestinal volvulus, a few reports have described cases of enteric duplication twisted on itself. We experienced a rare pediatric case of long-segment tubular ileal duplication showing torsion. Torsion of enteric duplication is extremely rare. We herein report a pediatric case showing unusual torsion of ileal duplication requiring emergency surgery. CASE PRESENTATION: A 3-year-old boy presented with abdominal pain and vomiting. Contrast-enhanced computed tomography (CT) revealed a cystic luminal structure with a blind end and fluid collection in the pelvic cavity. CT also showed no findings of ileus or intestinal dilatation except for a cystic luminal structure. The preoperative diagnosis was torsion of Meckel’s diverticulum. The patient underwent emergent explorative diagnostic laparoscopy. As a result, a necrotic luminal structure and bloody ascites were recognized, and small-scale laparotomy was performed. Long-segment ileal duplication was recognized. The long-segment tubular ileal duplication shared the anti-mesenteric side of the intestinal wall along one-third of its length. The residual two-thirds of its length was free from the ileum and its blind end was twisted in a manner that looked similar to Meckel’s diverticulum. Normal ileum and the duplication, including the twisted necrotic portion, were resected, and ileal anastomosis was performed. The postoperative course was uneventful. A pathological examination confirmed the definitive diagnosis of enteric duplication. CONCLUSIONS: We reported the unusual presentation of intestinal duplication mimicking torsion of Meckel’s diverticulum. Enteric duplication shows various clinical symptoms and presentations. We must understand that the classification of digestive enteric duplication is diverse with a variety of associated clinical symptoms. |
format | Online Article Text |
id | pubmed-8960505 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-89605052022-04-12 An unusual presentation of intestinal duplication mimicking torsion of Meckel’s diverticulum: a rare report of a pediatric case Matsukubo, Makoto Muto, Mitsuru Kedoin, Chihiro Matsui, Mayu Murakami, Masakazu Sugita, Koshiro Yano, Keisuke Onishi, Shun Harumatsu, Toshio Yamada, Koji Yamada, Waka Kaji, Tatsuru Ieiri, Satoshi Surg Case Rep Case Report BACKGROUND: Enteric duplication is a congenital disease that occurs throughout the entire gastrointestinal tract. Although it may sometimes cause intestinal volvulus, a few reports have described cases of enteric duplication twisted on itself. We experienced a rare pediatric case of long-segment tubular ileal duplication showing torsion. Torsion of enteric duplication is extremely rare. We herein report a pediatric case showing unusual torsion of ileal duplication requiring emergency surgery. CASE PRESENTATION: A 3-year-old boy presented with abdominal pain and vomiting. Contrast-enhanced computed tomography (CT) revealed a cystic luminal structure with a blind end and fluid collection in the pelvic cavity. CT also showed no findings of ileus or intestinal dilatation except for a cystic luminal structure. The preoperative diagnosis was torsion of Meckel’s diverticulum. The patient underwent emergent explorative diagnostic laparoscopy. As a result, a necrotic luminal structure and bloody ascites were recognized, and small-scale laparotomy was performed. Long-segment ileal duplication was recognized. The long-segment tubular ileal duplication shared the anti-mesenteric side of the intestinal wall along one-third of its length. The residual two-thirds of its length was free from the ileum and its blind end was twisted in a manner that looked similar to Meckel’s diverticulum. Normal ileum and the duplication, including the twisted necrotic portion, were resected, and ileal anastomosis was performed. The postoperative course was uneventful. A pathological examination confirmed the definitive diagnosis of enteric duplication. CONCLUSIONS: We reported the unusual presentation of intestinal duplication mimicking torsion of Meckel’s diverticulum. Enteric duplication shows various clinical symptoms and presentations. We must understand that the classification of digestive enteric duplication is diverse with a variety of associated clinical symptoms. Springer Berlin Heidelberg 2022-03-28 /pmc/articles/PMC8960505/ /pubmed/35344094 http://dx.doi.org/10.1186/s40792-022-01409-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Case Report Matsukubo, Makoto Muto, Mitsuru Kedoin, Chihiro Matsui, Mayu Murakami, Masakazu Sugita, Koshiro Yano, Keisuke Onishi, Shun Harumatsu, Toshio Yamada, Koji Yamada, Waka Kaji, Tatsuru Ieiri, Satoshi An unusual presentation of intestinal duplication mimicking torsion of Meckel’s diverticulum: a rare report of a pediatric case |
title | An unusual presentation of intestinal duplication mimicking torsion of Meckel’s diverticulum: a rare report of a pediatric case |
title_full | An unusual presentation of intestinal duplication mimicking torsion of Meckel’s diverticulum: a rare report of a pediatric case |
title_fullStr | An unusual presentation of intestinal duplication mimicking torsion of Meckel’s diverticulum: a rare report of a pediatric case |
title_full_unstemmed | An unusual presentation of intestinal duplication mimicking torsion of Meckel’s diverticulum: a rare report of a pediatric case |
title_short | An unusual presentation of intestinal duplication mimicking torsion of Meckel’s diverticulum: a rare report of a pediatric case |
title_sort | unusual presentation of intestinal duplication mimicking torsion of meckel’s diverticulum: a rare report of a pediatric case |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8960505/ https://www.ncbi.nlm.nih.gov/pubmed/35344094 http://dx.doi.org/10.1186/s40792-022-01409-6 |
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