Choledochal cyst type I in infant: a case report

Choledochal cysts are rare congenital anomalies characterized by dilatation of the bile ducts. The most frequent subtype of choledochal cyst is type I, which has fusiform dilatation of the common bile duct and poses significant challenges in diagnosis and management, particularly, in pediatric patie...

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Bibliographic Details
Main Authors: Steven Christian Susianto, Rendi Aji Prihaningtyas, Bagus Setyoboedi, Sarwendah Pratiwi Budiman, Fendy Matulatan, Sjamsul Arief
Format: Article
Language:English
Published: Amaltea Medical Publishing House 2024-06-01
Series:Romanian Journal of Pediatrics
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Online Access:https://rjp.com.ro/articles/2024.2/RJP_2024_2_Art-08.pdf
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Summary:Choledochal cysts are rare congenital anomalies characterized by dilatation of the bile ducts. The most frequent subtype of choledochal cyst is type I, which has fusiform dilatation of the common bile duct and poses significant challenges in diagnosis and management, particularly, in pediatric patients. We present a case report of a child diagnosed with a Type I choledochal cyst, detailing the clinical presentation, diagnostic workup, surgical intervention, and postoperative outcome. Early recognition and appropriate surgical management are crucial for optimal outcomes in children with this rare entity.
ISSN:1454-0398
2069-6175