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Thoracoabdominal duplication with hematochezia as an onset symptom in a baby: A case report

BACKGROUND: Alimentary tract duplication is a rare congenital disease that may occur in any part of the alimentary tract, whereas thoracoabdominal duplications only account for approximately 2% of all alimentary tract duplication cases. Many symptoms, including abdominal pain, abdominal distension,...

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Autores principales: Yang, Shao-Bo, Yang, Hong, Zheng, Shan, Chen, Gong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8409207/
https://www.ncbi.nlm.nih.gov/pubmed/34540987
http://dx.doi.org/10.12998/wjcc.v9.i24.7261
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author Yang, Shao-Bo
Yang, Hong
Zheng, Shan
Chen, Gong
author_facet Yang, Shao-Bo
Yang, Hong
Zheng, Shan
Chen, Gong
author_sort Yang, Shao-Bo
collection PubMed
description BACKGROUND: Alimentary tract duplication is a rare congenital disease that may occur in any part of the alimentary tract, whereas thoracoabdominal duplications only account for approximately 2% of all alimentary tract duplication cases. Many symptoms, including abdominal pain, abdominal distension, vomiting, gastrointestinal bleeding, chest discomfort, chest pain, and shortness of breath, may be present in patients with abdominal or thoracic duplication. CASE SUMMARY: A 10-mo-old infant, with a free previous medical history, was admitted to our hospital with melena three times in 6 d. Enhanced magnetic resonance imaging of the thoracic vertebrae revealed multiple cervicothoracic vertebral deformities, spina bifida, meningomyelocele towards the posterior mediastinum, and possible concurrent infection. Upper gastroenterography indicated intestinal malrotation. A laparoscopic abdominal examination was performed, and the operation was intraoperatively converted to laparotomy. This case was diagnosed intraoperatively as thoracoabdominal intestinal duplication. The intestinal duplications in the abdomen and large part of the thorax were excised. The results of postoperative pathological examination confirmed that this case was alimentary tract duplication and that part of the duplication contained gastric mucosa. The infant recovered well and was discharged 1 wk after the surgery. A follow-up computed tomography scan 3 mo after operation showed myelomeningocele while the posterior mediastinal cyst was significantly reduced. CONCLUSION: Thoracoabdominal duplication should be considered if a child has suspected abdominal intestinal duplication with hematochezia as an onset symptom.
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spelling pubmed-84092072021-09-16 Thoracoabdominal duplication with hematochezia as an onset symptom in a baby: A case report Yang, Shao-Bo Yang, Hong Zheng, Shan Chen, Gong World J Clin Cases Case Report BACKGROUND: Alimentary tract duplication is a rare congenital disease that may occur in any part of the alimentary tract, whereas thoracoabdominal duplications only account for approximately 2% of all alimentary tract duplication cases. Many symptoms, including abdominal pain, abdominal distension, vomiting, gastrointestinal bleeding, chest discomfort, chest pain, and shortness of breath, may be present in patients with abdominal or thoracic duplication. CASE SUMMARY: A 10-mo-old infant, with a free previous medical history, was admitted to our hospital with melena three times in 6 d. Enhanced magnetic resonance imaging of the thoracic vertebrae revealed multiple cervicothoracic vertebral deformities, spina bifida, meningomyelocele towards the posterior mediastinum, and possible concurrent infection. Upper gastroenterography indicated intestinal malrotation. A laparoscopic abdominal examination was performed, and the operation was intraoperatively converted to laparotomy. This case was diagnosed intraoperatively as thoracoabdominal intestinal duplication. The intestinal duplications in the abdomen and large part of the thorax were excised. The results of postoperative pathological examination confirmed that this case was alimentary tract duplication and that part of the duplication contained gastric mucosa. The infant recovered well and was discharged 1 wk after the surgery. A follow-up computed tomography scan 3 mo after operation showed myelomeningocele while the posterior mediastinal cyst was significantly reduced. CONCLUSION: Thoracoabdominal duplication should be considered if a child has suspected abdominal intestinal duplication with hematochezia as an onset symptom. Baishideng Publishing Group Inc 2021-08-26 2021-08-26 /pmc/articles/PMC8409207/ /pubmed/34540987 http://dx.doi.org/10.12998/wjcc.v9.i24.7261 Text en ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Case Report
Yang, Shao-Bo
Yang, Hong
Zheng, Shan
Chen, Gong
Thoracoabdominal duplication with hematochezia as an onset symptom in a baby: A case report
title Thoracoabdominal duplication with hematochezia as an onset symptom in a baby: A case report
title_full Thoracoabdominal duplication with hematochezia as an onset symptom in a baby: A case report
title_fullStr Thoracoabdominal duplication with hematochezia as an onset symptom in a baby: A case report
title_full_unstemmed Thoracoabdominal duplication with hematochezia as an onset symptom in a baby: A case report
title_short Thoracoabdominal duplication with hematochezia as an onset symptom in a baby: A case report
title_sort thoracoabdominal duplication with hematochezia as an onset symptom in a baby: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8409207/
https://www.ncbi.nlm.nih.gov/pubmed/34540987
http://dx.doi.org/10.12998/wjcc.v9.i24.7261
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