scholarly journals Cholangiocarcinoma Derived from Remnant Intrapancreatic Bile Duct Arising 32 Years after Congenital Choledochal Cyst Excision: A Case Report

2015 ◽  
Vol 8 (2) ◽  
pp. 265-273 ◽  
Author(s):  
Kentaro Ishikawa ◽  
Sadahisa Ogasawar ◽  
Tetsuhiro Chiba ◽  
Dai Sakamoto ◽  
Naoya Kanogawa ◽  
...  
Keyword(s):  
Case Report ◽  
Bile Duct ◽  
Choledochal Cyst ◽  
Congenital Choledochal Cyst ◽  
Cyst Excision ◽  
Intrapancreatic Bile Duct

Laparoscopic management of type VI choledochal cyst with common bile duct stone: report of a case and review of literature

2021 ◽  
Vol 14 (10) ◽  
pp. e244393
Author(s):  
G Revathi ◽  
Brijesh Kumar Singh ◽  
Yashwant Singh Rathore ◽  
Sunil Chumber
Keyword(s):  
Bile Duct ◽  
Common Bile Duct ◽  
Choledochal Cyst ◽  
Cystic Duct ◽  
Incidental Finding ◽  
Laparoscopic Approach ◽  
Biliary Colic ◽  
Type I ◽  
Laparoscopic Management ◽  
Cyst Excision

A young adult male presented with biliary colic and intermittent jaundice for 1 year. Abdomen findings were unremarkable. Routine investigations revealed a raised total bilirubin. On abdominal ultrasonography, common bile duct (CBD) dilatation with multiple stones was noted. On further imaging with magnetic resonance cholangiopancreatography, type I choledochal cyst (CDC) was suspected. A laparoscopic approach was planned. Intraoperatively, dilatation of cystic duct was noted which constitute type VI CDC. Partial malrotation of the gut and accessory right hepatic artery were also noted as incidental finding. Laparoscopic cholecystectomy with CBD exploration and removal of stones, biliary stent placement, cystic duct cyst excision and primary repair of CBD was done. Postoperatively, the patient improved symptomatically with a fall in bilirubin to normal range. We are describing the laparoscopic management of a rare case of type IV CDC which was diagnosed intraoperatively.

scholarly journals Intracholecystic papillary-tubular neoplasm in a patient with choledochal cyst and anomalous pancreaticobiliary junction: case report

2019 ◽  
Vol 5 (2) ◽  
pp. 20180079
Author(s):  
Marta Reis de Sousa ◽  
Inês Santiago ◽  
Maria J Barata ◽  
Mireia Castillo ◽  
Celso Matos
Keyword(s):  
Case Report ◽  
Bile Duct ◽  
Gastric Adenocarcinoma ◽  
Choledochal Cyst ◽  
Histopathological Analysis ◽  
Gallbladder Neoplasms ◽  
Choledochal Cysts ◽  
Bile Duct Dilatation ◽  
Duct Dilatation ◽  
Anomalous Pancreaticobiliary Junction

A 75-year-old female incidentally presented with an enhancing intraluminal gallbladder mass, main bile duct dilatation and anomalous pancreaticobiliary junction (APBJ) during the staging of gastric adenocarcinoma. Histopathological analysis confirmed the diagnosis of intracholecystic papillary-tubular neoplasm. Intracholecystic papillary-tubular neoplasms (ICPN) of the gallbladder are rare gallbladder neoplasms, defined as intramucosal, preinvasive, exophytic, mass forming lesions. An association between choledochal cysts and anomalous pancreaticobiliary junction with gallbladder neoplasms is well known, and this case potentially illustrates gallbladder carcinogenesis related to these biliary anomalies.

scholarly journals Congenital choledochal cyst

1973 ◽  
Vol 13 (1) ◽  
pp. 31
Author(s):  
Heyder Bin Heyder
Keyword(s):  
Bile Duct ◽  
Choledochal Cyst ◽  
Medical Literature ◽  
Personal Contact ◽  
Congenital Choledochal Cyst ◽  
Unusual Condition ◽  
The Pacific ◽  
The Common ◽  
The Right ◽  
Upper Abdomen

Although congenital choledochal cyst, a localized dilatation of the common bile duct, is an unusual condition in many countries, it should be expected in any infant who presents the triad of jaundice, tumor and pain in the right upper abdomen. Not less than 500 cases have been reported in the medical literature. Recently it is pointed out, that the congenital chledochal cyst is more common in Japan than in Europe or American countries. A personal contact with the Japanese delegation attending the meeting of the Pacific Association of Pediatric Surgeons in Vancouver, May 1971, confirmed it.

scholarly journals Biliary cancer developed after the reparative surgery for congenital choledochal cyst: a case report and review of the literature

2016 ◽  
Vol 6 (2) ◽  
pp. 43-49
Author(s):  
Kou Ikegame ◽  
Atsushi Takano ◽  
Hideki Watanabe ◽  
Atsushi Yamamoto ◽  
Yoshiaki Miyasaka ◽  
...  
Keyword(s):  
Case Report ◽  
Choledochal Cyst ◽  
Biliary Cancer ◽  
Review Of The Literature ◽  
Congenital Choledochal Cyst

Intrapancreatic Bile Duct Injury: Case Report

2002 ◽  
Vol 52 (4) ◽  
pp. 786-788 ◽  
Author(s):  
Sanjeev Kaul ◽  
Adena Homnick ◽  
David Livingston
Keyword(s):  
Case Report ◽  
Bile Duct ◽  
Bile Duct Injury ◽  
Intrapancreatic Bile Duct

scholarly journals Well-Differentiated Endocrine Carcinoma Originating From the Bile Duct in Association With a Congenital Choledochal Cyst

2013 ◽  
Vol 97 (4) ◽  
pp. 315-320 ◽  
Author(s):  
Kazuhiro Takahashi ◽  
Ryoko Sasaki ◽  
Yukio Oshiro ◽  
Kiyoshi Fukunaga ◽  
Tatsuya Oda ◽  
...  
Keyword(s):  
Bile Duct ◽  
Choledochal Cyst ◽  
Extrahepatic Bile Duct ◽  
Laboratory Data ◽  
World Health ◽  
Congenital Choledochal Cyst ◽  
Endocrine Carcinoma ◽  
Intrahepatic Bile Ducts ◽  
Extrahepatic Bile Duct Resection ◽  
Well Differentiated

Abstract We encountered a rare case of a well-differentiated endocrine carcinoma originating from the bile duct in association with a congenital choledochal cyst (CCC). The patient is a 28-year-old woman referred to our clinic for pruritus. Laboratory data showed mild elevation of serum hepatobiliary enzymes. Computed tomography and magnetic resonance imaging demonstrated pancreatobiliary maljunction and a Todani type IV-A CCC from the inferior bile duct to the bilateral intrahepatic bile ducts. A solid tumor was detected in the middle portion of the common bile duct. Pancreatoduodenectomy and total extrahepatic bile duct resection was performed. Based on pathologic and immunohistochemical examinations, a diagnosis of well-differentiated endocrine carcinoma was made according to the World Health Organization criteria. To our knowledge, this is the third report of a neuroendocrine tumor originating from the bile duct in association with a CCC.

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