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Updated: Feb 20, 2026

A Rat Model of Mild Intrauterine Hypoperfusion with Microcoil Stenosis
Published on: January 7, 2018
[CONGENITAL ILEAL STENOSIS: LATE CLINICAL MANIFESTATIONS OF EARLY PRENATAL SUSPICION]
Avi On1, Mary Abdo2, Sammi Haddad3
1Pediatric Gastroenterology Unit, Baruch Padeh Poriya Medical Center, affiliated with Bar-Ilan University Faculty of Medicine in the Galilee.
Congenital small intestine stenosis can present atypically in newborns. Early diagnosis is crucial, even with non-classic symptoms like diarrhea, to prevent delayed treatment of this rare obstruction.
Area of Science:
- Pediatric Surgery
- Neonatal Gastroenterology
Background:
- Congenital small intestine stenosis is a rare condition, often presenting later than complete obstruction (atresia).
- Delayed clinical manifestations can complicate diagnosis in neonates.
Observation:
- A neonate presented with prenatal ultrasound findings suggestive of small bowel obstruction.
- Postnatal clinical presentation and imaging were atypical, delaying surgical intervention for ileal stenosis.
Findings:
- Surgical resection of the stenotic ileum resolved vomiting but was followed by persistent diarrhea.
- Transitioning infant formula from long-chain triglycerides to medium-chain triglycerides effectively managed post-operative diarrhea.
Implications:
- Highlights the importance of considering congenital intestinal obstruction in neonates with vomiting, even with atypical symptoms like diarrhea.
- Emphasizes the need for prompt diagnosis and surgical management of small intestine stenosis, despite non-classic imaging findings.
- Demonstrates the therapeutic role of medium-chain triglyceride formulas in managing post-surgical malabsorption in infants.
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