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Isolated Infected Non-Communicating Enteric Duplication Cyst of Ileum in a Young Adult-Rare Case

Anand Bhandary Panambur^1*, Ashok Hegde¹, Anand Ignatius Peter¹ and Reba Philipose²

¹Department of General Surgery, A.J. Institute of Medical Sciences and Research Centre, Mangalore, India

²Department of Pathology, A.J. Institute of Medical Sciences and Research Centre, Mangalore, India

Received Date: Jun 20, 2022 / Published Date: Jul 18, 2022

Citation: Panambur AB, Hegde A, Peter AI, Philipose R (2022) Isolated Infected Non-Communicating Enteric Duplication Cyst of Ileum in a Young Adult-Rare Case. J Gastrointest Dig Syst 12:694.DOI: 10.4172/2161-069X.1000694

Copyright: © 2022 Panambur AB, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Enteric duplication cysts are rare and uncommon congenital anomalies that arise during the embryonic period of the human digestive system's development. They are most commonly seen in infancy or early childhood, but they are seldom seen in adulthood. Due to the rarity of this anomaly, the vast bulk of literature on enteric duplication cysts is in the form of case reports, mostly among pediatric population. We present a rare case of infected isolated non communicating enteric duplication cyst in a 25 year male patient who presented with clinical diagnosis of acute appendicitis. Resection of the duplication cyst was performed safely without requiring bowel resection.

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