Abstract

A choledochal cyst involving the cystic duct (type 6) is a rare disease. Dilatation of the common bile duct along with the involvement of cystic duct is extremely rare and only a few cases have been reported until now. A 38-year-old woman was evaluated for complaints of pain in the upper abdomen. On initial imaging with ultrasonography (USG) and magnetic resonance cholangiopancreatography (MRCP), she was diagnosed to have a type 1a choledochal cyst. Intraoperatively we found that it was not a simple cystic dilatation of the common bile duct (CBD) alone but the cystic duct was also dilated. Simple cholecystectomy with excision of the cyst and reconstruction with a Roux en Y hepaticojejunostomy was performed. The patient is doing well after six months of follow up. This type of choledochal cyst (CDC) with combined dilatation of cystic duct and CBD has not been defined in the Todani classification. Two studies published until now have given their own extension of the Todani classification as either type 1D or 6B. Our another case where a 23-year-old female with similar complaints was diagnosed with an isolated cystic duct dilatation (type 6A); here, we did a simple laparoscopic cholecystectomy. Thus, we need to know that these distinct type of choledochal cyst exists and has to be added to the classification. It is also important to classify type 6 into two types A and B as their management differs.

Highlights

  • Choledochal cysts are either congenital or acquired dilatation of the biliary tree involving either the intrahepatic or extrahepatic biliary radicals or both

  • We present first an extremely rare case of combined dilatation of the common bile duct and cystic duct in a 38-year-old female evaluated for upper abdominal pain in our institution

  • She was diagnosed to have type 1 choledochal cyst but intraoperatively we found involvement of the cystic duct. This type of presentation is very rare and few cases have been reported in the literature earlier, but these have not been included in the Todani classification and are not standardized. Some have reported these as a variant of type 6-type 6B involving combined dilatation of cystic duct as well as the common bile duct (CBD) [3]

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Summary

Introduction

Choledochal cysts are either congenital or acquired dilatation of the biliary tree involving either the intrahepatic or extrahepatic biliary radicals or both. We present first an extremely rare case of combined dilatation of the common bile duct and cystic duct in a 38-year-old female evaluated for upper abdominal pain in our institution She was diagnosed to have type 1 choledochal cyst but intraoperatively we found involvement of the cystic duct . This type of presentation is very rare and few cases have been reported in the literature earlier, but these have not been included in the Todani classification and are not standardized. There are many cases being reported in the literature with combined dilatation of cystic duct and rest of biliary tract We present these cases to appreciate this type of choledochal cyst as a distinct entity and addition to the existing literature, for a standardized classification for these variants. She is doing well after five years of follow-up

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