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Updated: Jun 2, 2026

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Published on: March 17, 2026
Duodenal stenosis in a child
A Y Kshirsagar1, Sanjitsingh R Sulhyan, Gaurav Vasisth
1Department of Surgery, Krishna Institute of Medical Sciences University, Karad, Maharashtra, India. drayk@indiatimes.com
Delayed diagnosis of incomplete duodenal obstruction, such as duodenal stenosis or atresia, presents challenges. However, with prompt intervention, survival rates for these congenital conditions remain high.
Area of Science:
- Pediatric Surgery
- Neonatal Medicine
- Gastrointestinal Development
Background:
- Duodenal atresia arises from failed duodenal lumen recanalization between the 8th-10th gestational weeks.
- Incomplete recanalization can manifest as duodenal stenosis or a duodenal web.
- Congenital duodenal obstructions require timely diagnosis and management.
Observation:
- This case highlights a delayed presentation of incomplete duodenal obstruction.
- Delayed diagnosis complicates the diagnostic process and intervention timing.
- The specific clinical presentation and diagnostic challenges are detailed.
Findings:
- Incomplete duodenal obstruction, including stenosis and atresia, is addressed.
- The etiology linked to failed embryonic recanalization is discussed.
- High survival rates are noted when diagnosed and treated, especially without comorbidities.
Implications:
- Emphasizes the importance of early recognition of congenital duodenal anomalies.
- Highlights the need for advanced diagnostic imaging and surgical planning.
- Underscores the favorable prognosis for duodenal stenosis and atresia with appropriate care.
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