Spontaneous Rupture of Choledochal Cyst: A Rare Presentation
نویسندگان
چکیده
Abstract Choledochal cyst (CDC) is a rare surgical cause of cholestatic jaundice in infants. Spontaneous rupture an unusual presentation previously undiagnosed CDC and also biliary peritonitis children. Here, we report case 1-year-old boy who was evaluated for progressive abdominal distension. Ultrasonogram showed gross ascites with echogenic particles, dilated common bile duct (CBD), hepatic (CHD), upstream intra radicle dilatation (IHBRD). CECT sections the abdomen IHBRD disproportionate CHD CBD. At laparotomy, type 1 anterior wall found. The excised followed by hepaticojejunostomy. In sick child pain, ascites, high index suspicion during imaging will help correct diagnosis surgery potentially fatal ruptured CDC.
منابع مشابه
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ژورنال
عنوان ژورنال: Journal of Gastriontestinal and Abdominal Radiology ISGAR
سال: 2023
ISSN: ['2581-9178']
DOI: https://doi.org/10.1055/s-0042-1759682