Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
4161143 | Journal of Pediatric Surgery Case Reports | 2016 | 5 Pages |
Abstract
•10-year old presented with abdominal pain, diagnosed through ERCP as 5 cm, type III choledochal cyst.•Upon open exploration, the choledochocele was noted to be lined by intestinal mucosa.•A transduodenal subtotal cyst excision with extensive sphincteroplasty was performed.•18 month follow up uneventful.
Choledochal cysts are rare congenital anomalies of the biliary tree which may progress to obstruction or malignancy. Of the five Todani variants, choledochocele, or type III choledochal cyst is the rarest. In this case report, we describe a previously healthy 10-year old female who presented with a choledochocele and was treated by near-total excision with transposition of the common channel, resulting in an extended sphincteroplasty.
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Authors
Inna N. Lobeck, Phylicia Dupree, Richard A. Falcone Jr., Tom K. Lin, Andrew T. Trout, Jaimie D. Nathan, Greg M. Tiao,