Diagnostic Dilemma Between Todani Type II Choledochal Cyst and Duplication of Gallblader in an Adult Patient

2020 ◽  
Vol 92 (2) ◽  
pp. 85-87
Author(s):  
Michail L Lorentziadis ◽  
Amir Mounir Hussein ◽  
Moustafa Mahmoud Nafady Hego ◽  
Ghada M Almakhaita
2021 ◽  
Vol 14 (2) ◽  
pp. e238971
Author(s):  
Anish Chowdhury ◽  
Cherring Tandup ◽  
Amaresh Aruni ◽  
Vanji Nathan Subramani

Choledochal cyst and gallbladder duplication are rare congenital anomalies. They typically are surgical problems of infancy or childhood but rarely may present in adults also. Despite high resolution imaging, the differentiation of type II choledochal cyst from gallbladder duplication often causes the diagnostic dilemma; which may result in high risk for intraoperative iatrogenic injury. Operative management of choledochal cyst is the definite treatment because of its malignant potential. A type II choledochal cyst arising from the hepatic hilum presenting as gallbladder duplication on imaging has not been reported earlier in the literature and here we present a case report of the same which was managed successfully.


2021 ◽  
Author(s):  
Atsushi Yamaguchi ◽  
Hirotaka Kouno ◽  
Hiroshi Kohn

2021 ◽  
Vol 17 (2) ◽  
pp. 259
Author(s):  
Rekha Arcot ◽  
Arihanth Ravichandran ◽  
Anbalagan Pichaimuthu

2020 ◽  
Vol 27 (10) ◽  
pp. 789-790
Author(s):  
Jun Suh Lee ◽  
Yoo‐Seok Yoon ◽  
Ho‐Seong Han ◽  
Junyub Kim ◽  
Boram Lee ◽  
...  

2019 ◽  
Vol 22 (2) ◽  
pp. 38-40
Author(s):  
Tul Maya Gurung ◽  
Rabin Koirala ◽  
Amit Shrestha

Choledochal cysts are rare congenital anomalies that have a variable presentation with occasional diagnostic and therapeutic dilemmas. Our case is a 14-year female presented with recurrent abdomen pain with confusing diagnostic findings, suggestive of a large choledochal cyst (22x29x17cm) initially managed by percutaneous tube biliary drainage and later underwent excision and HPE revealing non-malignant findings. The choledochal cyst should always be a differential diagnosis for any patient presenting with an abdominal mass and should be managed accordingly.


2018 ◽  
Vol 100 (2) ◽  
pp. e34-e37 ◽  
Author(s):  
R Kilambi ◽  
AN Singh ◽  
KS Madhusudhan ◽  
P Das ◽  
S Pal

Isolated choledochal cysts involving the cystic duct are rare. We present a case of a choledochal cyst involving only the proximal cystic duct, and discuss the taxonomic and therapeutic challenges. There is a need for a clearly defined classification system for these cysts as they may be categorised as either type II or type VI cysts. The optimal treatment remains debatable, with some authors recommending a bilioenteric reconstruction owing to the wide cystic duct–bile duct junction. However, we suggest that a cholecystectomy should be performed with examination of the specimen and frozen section in case of any abnormality rather than upfront bile duct excision. In addition, given the rarity of this condition and the paucity of long-term data, we recommend meticulous follow-up for development of any malignancy.


2020 ◽  
Vol 26 (1) ◽  
pp. 33
Author(s):  
Jeesun Kim ◽  
Dayoung Ko ◽  
Ji-Won Han ◽  
Hyun-Young Kim

Sign in / Sign up

Export Citation Format

Share Document