RARE DELAYED PRESENTATION OF DUODENAL ATRESIA WITH ANNULAR PANCREAS: A CASE REPORT

Authors

  • DIVYA PRIYA S S POSTGRADUATE, DEPARTMENT OF GENERAL SURGERY, SAVEETHA MEDICAL COLLEGE AND HOSPITAL, CHENNAI
  • JAI DURAIRAJ P PROFESSOR, SAVEETHA MEDICAL COLLEGE AND HOSPITAL, CHENNAI
  • KEERTHIKA M

Abstract

Background: Duodenal atresia is a congenital gastrointestinal obstruction caused by failure of fetal duodenal recanalization. Although it commonly presents in the neonatal period with bilious vomiting, atypical delayed presentations are increasingly recognized, particularly in Type 1 atresia (duodenal web).

Case Presentation: We describe an 11-month-old infant with a 6-month history of recurrent non-bilious vomiting, intolerance to solids, and failure to thrive. Imaging suggested proximal duodenal obstruction, while intraoperative findings revealed Type 1 duodenal atresia due to a duodenal web, compounded by annular pancreas. Surgical correction was achieved via Kimura’s diamond-shaped duodenoduodenostomy.

Outcome: The infant had an uneventful recovery, with resolution of vomiting, tolerance of regular diet, and significant catch-up growth.

Conclusion: This case highlights the importance of maintaining suspicion for congenital duodenal obstruction beyond the neonatal period. Annular pancreas in conjunction with a duodenal web adds diagnostic and operative complexity, but timely recognition and Kimura’s duodenoduodenostomy provide excellent outcomes.

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How to Cite

S S, D. P., P, J. D., & M, K. (2025). RARE DELAYED PRESENTATION OF DUODENAL ATRESIA WITH ANNULAR PANCREAS: A CASE REPORT. TPM – Testing, Psychometrics, Methodology in Applied Psychology, 32(S2(2025) : Posted 09 June), 2069–2072. Retrieved from https://tpmap.org/submission/index.php/tpm/article/view/1077