Type 1a Duodenojejunal Tubular Duplication Cyst with Complex Rotational Anomaly Masquerading as Chronic Anemia

Priya Mathew1, Ankur Mandelia1, Amit Buan1

  • 1Department of Pediatric Surgery, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.

Insights

This case report highlights a rare instance of a 4-year-old girl with chronic anemia caused by co-occurring enteric duplication cysts and reversed intestinal rotation (RIR). Surgical intervention successfully resolved the condition.

Area of Science:

  • Pediatric Surgery
  • Congenital Anomalies
  • Gastrointestinal Motility Disorders

Background:

  • Enteric duplication cysts and reversed intestinal rotation (RIR) are rare congenital anomalies.
  • Their coexistence is exceptionally uncommon, presenting diagnostic challenges.

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