{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,28]],"date-time":"2026-02-28T09:15:23Z","timestamp":1772270123283,"version":"3.50.1"},"reference-count":9,"publisher":"Oxford University Press (OUP)","issue":"3","license":[{"start":{"date-parts":[[2022,3,31]],"date-time":"2022-03-31T00:00:00Z","timestamp":1648684800000},"content-version":"vor","delay-in-days":30,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2022,3,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:p>Type VI choledochal cysts or cystic duct dilatation cysts are a relatively new and rare condition. We report the case of a 35-year-old man who presented with a history of recurrent episodes of epigastrium pain. Magnetic resonance cholangiography revealed a cyst lodged between the cystic duct and the right anterior sectoral bile duct. He underwent a laparoscopic right anterior sectorectomy with cholecystectomy. Pathological examination revealed a cyst with a fibrous wall, dense chronic inflammatory infiltration, lined by columnar epithelium. Due to its rarity, the diagnosis is often made intraoperatively. The treatment of cystic duct cysts includes cholecystectomy, complete cyst excision, recontinuity of the common bile duct. Type VI choledochal cysts are extremely rare. Preoperative diagnosis, using either magnetic resonance cholangiopancreatography or endoscopic retrograde cholangiopancreatography, is vital to prevent postoperative complications. Treatment of this type of cysts includes cholecystectomy and complete cyst excision and biliary-enteric reconstruction if necessary.<\/jats:p>","DOI":"10.1093\/jscr\/rjac126","type":"journal-article","created":{"date-parts":[[2022,3,11]],"date-time":"2022-03-11T20:09:55Z","timestamp":1647029395000},"source":"Crossref","is-referenced-by-count":2,"title":["Choledochal cysts type VI: biliary cyst of the cystic duct with connecting to right anterior sectoral bile duct: a case report"],"prefix":"10.1093","volume":"2022","author":[{"given":"Nattaporn","family":"Maneepairoj","sequence":"first","affiliation":[{"name":"Division of HPB Surgery, Department of Surgery, Phramongkutklao Hospital, Thung Phaya Thai, Ratchathewi, Bangkok, Thailand"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Pipit","family":"Burasakarn","sequence":"additional","affiliation":[{"name":"Division of HPB Surgery, Department of Surgery, Phramongkutklao Hospital, Thung Phaya Thai, Ratchathewi, Bangkok, Thailand"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Anuparp","family":"Thienhiran","sequence":"additional","affiliation":[{"name":"Division of HPB Surgery, Department of Surgery, Phramongkutklao Hospital, Thung Phaya Thai, Ratchathewi, Bangkok, Thailand"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Pusit","family":"Fuengfoo","sequence":"additional","affiliation":[{"name":"Division of HPB Surgery, Department of Surgery, Phramongkutklao Hospital, Thung Phaya Thai, Ratchathewi, Bangkok, Thailand"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sutdhachit","family":"Linananda","sequence":"additional","affiliation":[{"name":"Division of HPB Surgery, Department of Surgery, Phramongkutklao Hospital, Thung Phaya Thai, Ratchathewi, Bangkok, Thailand"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sermsak","family":"Hongjinda","sequence":"additional","affiliation":[{"name":"Division of HPB Surgery, Department of Surgery, Phramongkutklao Hospital, Thung Phaya Thai, Ratchathewi, Bangkok, Thailand"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"286","published-online":{"date-parts":[[2022,3,30]]},"reference":[{"key":"2022033108135859800_ref1","doi-asserted-by":"crossref","first-page":"263","DOI":"10.1016\/0002-9610(77)90359-2","article-title":"Congenital bile duct cysts: classification, operative procedures, and review of thirty-seven cases including cancer arising from choledochal cyst","volume":"134","author":"Todani","year":"1977","journal-title":"Am J Surg"},{"key":"2022033108135859800_ref2","first-page":"320","article-title":"Cystic dilatation of the cystic duct: a new type of biliary cyst","volume":"109","author":"Serradel","year":"1991","journal-title":"Surgery"},{"key":"2022033108135859800_ref3","doi-asserted-by":"crossref","first-page":"828","DOI":"10.1016\/0002-9610(83)90152-6","article-title":"Isolated cystic dilatation of the cystic duct","volume":"145","author":"Bode","year":"1983","journal-title":"Am J Surg"},{"key":"2022033108135859800_ref4","first-page":"e91","article-title":"Type VI choledochal cyst revisited","volume":"52","author":"De","year":"2011","journal-title":"Singapore Med J"},{"key":"2022033108135859800_ref5","first-page":"190","article-title":"Pancreatico-biliary ductal union","volume":"22","author":"Bheerappa","year":"2001","journal-title":"Trop Gastroenterol"},{"key":"2022033108135859800_ref6","first-page":"12","article-title":"Type IV choledochal cyst with gall bladder carcinoma","volume":"29","author":"Vishwanath","year":"2019","journal-title":"BMJ Case Rep"},{"key":"2022033108135859800_ref7","doi-asserted-by":"crossref","first-page":"619","DOI":"10.2214\/ajr.173.3.10470889","article-title":"Choledochal cyst an unusual type of cystic dilatation of the cystic duct","volume":"173","author":"Loke","year":"1999","journal-title":"Am J Roentgenol"},{"key":"2022033108135859800_ref8","doi-asserted-by":"crossref","first-page":"e82","DOI":"10.1055\/s-0039-1693652","article-title":"Type VI choledochal cysts-case report and review of literature","volume":"5","author":"Amarjothi","year":"2019","journal-title":"Surg J"},{"key":"2022033108135859800_ref9","doi-asserted-by":"crossref","first-page":"458","DOI":"10.1016\/j.vgie.2019.07.005","article-title":"Type VI choledochal cyst diagnosed on ERCP with direct cholangioscopy","volume":"4","author":"Ku","year":"2019","journal-title":"VideoGIE"}],"container-title":["Journal of Surgical Case 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