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Published on: August 23, 2022
Congenital duodenal obstruction with delayed presentation: seven years of experience
Seyed Abdollah Mousavi1, Hasan Karami2, Hossein Saneian3
1Department of Pediatric Surgery, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Insights
Congenital duodenal webs can cause later-age obstruction, presenting as failure to thrive. Early diagnosis of these duodenal obstructions is crucial for better outcomes.
Area of Science:
- Pediatric Surgery
- Gastroenterology
- Congenital Malformations
Background:
- Congenital intestinal obstruction commonly affects the duodenum.
- Duodenal webs with fenestrations may not show immediate signs of obstruction.
- Late presentation can lead to significant complications.
Purpose of the Study:
- To evaluate complications and operative findings in children with congenital intestinal obstruction.
- To analyze cases of duodenal webs presenting later in childhood.
- To highlight the importance of timely diagnosis.
Main Methods:
- Retrospective review of pediatric congenital intestinal obstruction cases over 7 years.
- Analysis of operative findings, including duodenal atresia, annular pancreas, malrotation, and fenestrated duodenal webs.
- Evaluation of patient demographics, associated conditions (e.g., trisomy 21), and clinical presentations.
Main Results:
- 81 infants with congenital intestinal obstruction were identified.
- Fenestrated duodenal webs were found in 8 patients, with ages ranging from 5 days to 72 months.
- Late-presenting patients (over 2 years) experienced complications like gastroesophageal reflux, esophageal ulcer, stricture, and dysphagia. A unique case involved a patient with a massive fruit seed bezoar.
Conclusions:
- Duodenal webs can present subtly in later childhood with failure to thrive and food intolerance, mimicking other conditions.
- A high index of suspicion is vital for diagnosing duodenal webs presenting beyond the typical neonatal period.
- Prompt diagnosis and intervention are essential to prevent severe complications associated with congenital duodenal obstruction.
Introduction:
The duodenum is the most common site for congenital intestinal obstruction. The duodenal web with a central hole can present without any overt signs of obstruction at a later age.
Material And Methods:
Over a 7-year period, children with congenital intestinal obstruction were identified in this study. The complications and operative findings of patients with duodenal web with conditions such as wind sock deformity and delayed diagnosis were evaluated in this study.
Results:
This study included 81 infants with congenital intestinal obstruction. At operation, 48 patients demonstrated duodenal obstruction with atresia in 27, annular pancreas in 15 and malrotation in 6. Also, we observed incomplete obstruction of the duodenum due to a fenestrated web in 8 patients. The age of these patients at operation time ranged from 5 days to 72 months. Fifty percent of affected patients were associated with trisomy 21, all of whom exhibited failure to thrive due to food intolerance. The patients older than 2 years presented with major complications of gastroesophageal reflux such as esophageal ulcer, stricture and dysphagia. Additionally we had a unique case of a patient who had been referred with an epigastric mass. During the operation, we found 440 seeds of various fruits in the stomach and the first portion of the duodenum.
Conclusions:
Our study emphasizes that duodenal web with a central hole can present without signs of obstruction at a later age with only failure to thrive and food intolerance. Therefore a high index of suspicion is necessary for diagnosis when it presents beyond the usual age.
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