Ileocecal Valve Atresia - A Take on the Aberrant Phenomenon

Anup Kumar Panigrahi1, Priyanka Anvekar2, Petras Lohana3

  • 1Minimal Access Surgery, Safdarjung Hospital and Lohia Hospital, New Delhi, IND.

Cureus
|October 14, 2021
PubMed

Insights

Ileocecal valve atresia, a rare gastrointestinal obstruction, is detailed in this case report. Surgical intervention led to a successful recovery in a neonate.

Area of Science:

  • Pediatric Surgery
  • Gastrointestinal Malformations
  • Neonatal Care

Background:

  • Ileocecal valve atresia is an exceptionally rare congenital anomaly.
  • It presents as a severe form of intestinal obstruction in newborns.
  • Few documented cases exist in medical literature.

Observation:

  • A one-day-old male infant presented with symptoms of intestinal obstruction.
  • Emergency laparotomy revealed atresia of the ileocecal valve.

Findings:

  • Surgical resection of the atretic segment was performed.
  • An anastomosis was created following resection.
  • The infant experienced a positive postoperative recovery.

Implications:

  • This case highlights the importance of recognizing and managing rare gastrointestinal atresias.
  • Successful surgical outcomes are achievable with prompt intervention.
  • Further documentation of such rare cases aids in understanding and treatment protocols.

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