1. Congenital intrathoracic stomach can be safely managed laparoscopically.
- Author
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Gupta A, Zia B, Mullassery D, De Coppi P, Giuliani S, Curry JI, and Cross KM
- Subjects
- Child, Preschool, Female, Hernia, Hiatal congenital, Hernia, Hiatal diagnosis, Humans, Infant, Infant, Newborn, Male, Recurrence, Retrospective Studies, Fundoplication methods, Gastrostomy methods, Hernia, Hiatal surgery, Herniorrhaphy methods, Laparoscopy methods, Stomach surgery
- Abstract
Purpose: Congenital intrathoracic stomach (CIS) is an uncommon pediatric surgical diagnosis where > 2/3rd of the stomach lies within the chest through a hiatus defect. We reviewed our recent experience with this condition., Methods: A retrospective single-center review of children with a diagnosis of CIS (2007-2018) was performed. Patient demographics, presentation, imaging and management were assessed. Results are expressed as median (range)., Results: Eleven patients (6 girls) were identified with onset of symptoms at 2 (0-26) months of age. Presenting symptoms were vomiting (8/11), respiratory symptoms (4/11) and failure to thrive (2/11). Two patients had Marfan's syndrome. An upper gastrointestinal contrast study demonstrated gastric herniation in all. All were corrected laparoscopically with hiatus repair and fundoplication [age at surgery 10.5 (1.5-34.5) months]. A concurrent gastrostomy was done in children ≤ 6 months (n = 5). Enteral feeds were commenced on post-operative day one in 9 and second post-operative day in 2. At 7 (0-95) months follow-up, all were on full enteral feeds. One patient had a recurrence 6 months post-operatively, which was re-operated laparoscopically without any further recurrence., Conclusion: This is the largest reported series of children with CIS. All could be managed laparoscopically with no conversions and a low recurrence.
- Published
- 2020
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