Results 81 to 90 of about 73,738 (208)

Choledochal cyst as a diagnostic pitfall: a case report [PDF]

open access: yes, 2008
Introduction Choledochal cysts are rare congenital anomalies. Their diagnosis is difficult, particulary in adults. Case presentation This case report demonstrates the diagnostic and therapeutic pitfalls.
Doris Henne-Bruns   +5 more
core   +2 more sources

A Choledochal Cyst Resulting in Obstructive Jaundice in a Case with Gallbladder Agenesis: Report of a Case and Review of the Literature

open access: yesBalkan Medical Journal, 2012
Co-existence of gallbladder agenesis and choledochal cyst is a very rare congenital anomaly of the extrahepatic biliary system. The literature presents only five cases with this combination. Herein, we report the sixth case.
Abdullah Böyük   +4 more
doaj  

Giant Choledochal Cyst in an Adult at a Teaching Hospital in South-Western Uganda: A Case Report

open access: yesInternational Medical Case Reports Journal, 2021
Mvuyo Maqhawe Sikhondze,1 Carlos Cabrera Dreque,1 Edson Tayebwa,1 Gotharido Tumubugane,1 Charles Newton Odongo,1 Eugene Ogwang2 1Department of Surgery, Mbarara University of Science and Technology, Mbarara City, South-Western Uganda, Uganda; 2Department ...
Sikhondze MM   +5 more
doaj  

Cisto de colédoco: relato de caso e revisão da literatura. [PDF]

open access: yes, 1998
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Departamento de Pediatria, Curso de Medicina, Florianópolis ...
Ozelame, Rodrigo Vieira
core  

Anomalous pancreaticobiliary junction and new-onset biliary dilation: A case series

open access: yesJournal of Pediatric Surgery Case Reports
Introduction: Choledochal cysts are characterized by dilation of the biliary tree with uncertain etiology. It has been theorized that an anomalous pancreaticobiliary junction (APBJ), a congenital malformation in which the pancreatic and bile ducts join ...
Raissa Li   +5 more
doaj   +1 more source

A Choledochal Cyst in a Child Female [PDF]

open access: yes, 2014
Choledochal cysts are rare congenital anomalies. Diagnosis can be made by ultrasonography, CT-scan, endoscopic retrograde cholangiopancreatography (ERCP) and MRCP. The recurrent cholangitis, pancreatitis and malignant diseases associated with choledochal
Jumman, Najwa Aziz   +2 more
core   +1 more source

Laparoscopic resection of type I choledochal cyst

open access: yes, 2003
Type I choledochal cyst is a rare saccular or fusiform congenital dilatation of the extrahepatic biliary tract. It is usually treated by laparotomy at which the cyst is completely excised and a Roux-en-Y hepaticojejunostomy is performed to establish ...
Tan, H. L.   +2 more
core   +1 more source

Choledochal cyst type I in infant: a case report [PDF]

open access: yesRomanian Journal of Pediatrics
Choledochal cysts are rare congenital anomalies characterized by dilatation of the bile ducts. The most frequent subtype of choledochal cyst is type I, which has fusiform dilatation of the common bile duct and poses significant challenges in diagnosis ...
Steven Christian Susianto   +5 more
doaj   +1 more source

Simultaneous choledochal cyst excision and pancreaticojejunostomy (Puestow’s technique) for type IA cyst with associated chronic pancreatitis: a case report

open access: yesEgyptian Liver Journal
Introduction and importance Choledochal cysts are congenital conditions that affect the biliary tree, typically identified during childhood. These cysts present as dilations in the biliary system, occurring either in the extrahepatic or intrahepatic ...
Hamza Bashir   +2 more
doaj   +1 more source

Modified method of T-tube placement in cases of ruptured choledochal cyst having complete loss of anterior wall

open access: yesThe Saudi Journal of Gastroenterology, 2011
Survival rates for infants and children who have choledochal cyst with or without spontaneous rupture have improved dramatically in the past decades. Despite excellent long-term survival for patients with choledochal cyst who undergo elective surgery ...
Ahmed Intezar   +5 more
doaj   +1 more source

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