Continuous Thoraco-Abdominal Duplication in Children Type Ia: Case Report

Introduction: Thoraco-abdominal duplications, rare malformations of the oesophagus gastrointestinal tract, present diagnostic challenges often requiring surgical confirmation. Observation: A 22-month-old male with a thoraco-abdominal mass. After laparotomy, histological analysis confirmed an esophagogastroduodenal duplication extending from the esophagus to the duodenum. Discussion: The esophagogastroduodenal duplication extending from the esophagus to the duodenum is rare, with variable presentation and embryological origins. Clinical manifestations vary, imaging aids diagnosis, and surgery is the definitive treatment. Conclusion: This case underscores the importance of prompt identification and management of digestive duplications, emphasizing the necessity of resection and potential adjacent tissue involvement.

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Publication Details

Journal
Scholars Journal of Medical Case Reports
Published
2025-02-19
DOI
https://doi.org/10.36347/sjmcr.2025.v13i02.010
Primary Topic
Gastrointestinal disorders and treatments
Type
article
Field-Weighted Citation Impact
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article

Continuous Thoraco-Abdominal Duplication in Children Type Ia: Case Report

Rihab Sadqi, Hicham Zerhouni, Mounir Kisra, Monim Ochan et al.
Scholars Journal of Medical Case Reports
Gastrointestinal disorders and treatments
article

Continuous Thoraco-Abdominal Duplication in Children Type Ia: Case Report

Rihab Sadqi, Hicham Zerhouni, Mounir Kisra, Monim Ochan, Ahmed El Baoudi
article en

Abstract

Introduction: Thoraco-abdominal duplications, rare malformations of the oesophagus gastrointestinal tract, present diagnostic challenges often requiring surgical confirmation. Observation: A 22-month-old male with a thoraco-abdominal mass. After laparotomy, histological analysis confirmed an esophagogastroduodenal duplication extending from the esophagus to the duodenum. Discussion: The esophagogastroduodenal duplication extending from the esophagus to the duodenum is rare, with variable presentation and embryological origins. Clinical manifestations vary, imaging aids diagnosis, and surgery is the definitive treatment. Conclusion: This case underscores the importance of prompt identification and management of digestive duplications, emphasizing the necessity of resection and potential adjacent tissue involvement.

Scholars Journal of Medical Case ReportsVol. 13(02)
Openalex Percentile: Top 94%
Gastrointestinal disorders and treatments
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