| Literature DB >> 29884662 |
Muhammad Arshad1,2, Sarah Masroor Jeelani3, Asma Siddiqui2, Rana Rehan4.
Abstract
Alimentary tract duplications are a rare congenital malformation. They can present with varied symptoms owing to the locality of the duplication, along the gastrointestinal tract. Out of these duplications, the ones along the pylorus are the most rare. These are usually only diagnosed intraoperatively, as it is not a common differential on imaging due to its rarity. In lieu of the literature currently available, pyloric duplication cyst can present anytime from 1 week of age to 5 years, with some cases being detected antenatally due to the prevalence of regular antenatal scanning. Surgery remains the main stay of treatment with the goal of complete excision of the cyst and complete removal of the cyst mucosal lining. We report the case of a 5-year-old girl, which to our knowledge is the first ever reported case from Karachi, Pakistan. © BMJ Publishing Group Ltd (unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.Entities:
Keywords: congenital disorders; paediatric surgery
Mesh:
Year: 2018 PMID: 29884662 PMCID: PMC6011471 DOI: 10.1136/bcr-2017-223384
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X