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Neonatal intestinal obstruction due to double jejunal web causing Windsock deformity
Aejaz A Baba1, Altaf H Shera, Afak Y Sherwani
1Department of Pediatric Surgery, SKIMS, Srinagar, J&K, India.
Journal of Indian Association of Pediatric Surgeons
|December 3, 2010
Summary
Windsock deformity, a rare condition, can cause neonatal intestinal obstruction. This report details a unique case involving double jejunal webs and windsock deformity in an infant.
Area of Science:
- Medical case report
- Pediatric surgery
- Gastrointestinal anomalies
Background:
- Windsock deformity (WD) is an uncommon congenital anomaly affecting the gastrointestinal tract.
- Neonatal intestinal obstruction presents a critical surgical challenge in newborns.
- Jejunal webs are intrinsic obstructions of the small intestine, often presenting in infancy.
Observation:
- This report describes a rare case of a neonate presenting with symptoms of intestinal obstruction.
- The obstruction was attributed to a combination of double jejunal webs and windsock deformity.
- Diagnostic imaging confirmed the presence of these co-occurring anomalies.
Findings:
- The surgical findings revealed a complex anatomical abnormality involving the jejunum.
- Successful surgical intervention was performed to relieve the obstruction caused by the double jejunal webs and WD.
- Histopathological examination confirmed the nature of the defects.
Implications:
- This case highlights the importance of considering rare anomalies in the differential diagnosis of neonatal intestinal obstruction.
- Understanding the coexistence of jejunal webs and windsock deformity can improve diagnostic accuracy.
- Such reports contribute to the limited literature on complex gastrointestinal malformations in neonates, aiding future clinical management and research.
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