A Choledochal Cyst Resulting In Obstructive Jaundice In A Case With Gallbladder Agenesis: Report Of A Case And Review Of The Literature

2010 ◽  
Author(s):  
Abdullah Boyuk ◽  
Cuneyt Kirkil ◽  
Koray Karabulut ◽  
Selim Sozen ◽  
Salih Demirelli
Keyword(s):  
Obstructive Jaundice ◽  
Choledochal Cyst ◽  
Review Of The Literature ◽  
Gallbladder Agenesis

scholarly journals Obstructive jaundice due to a blood clot after ERCP: a case report and review of the literature

2018 ◽  
Vol 18 (1) ◽  
Author(s):  
Yangbei Zhu ◽  
Shuling Wang ◽  
Shengbing Zhao ◽  
Lin Qi ◽  
Zhaoshen Li ◽  
...  
Keyword(s):  
Case Report ◽  
Obstructive Jaundice ◽  
Blood Clot ◽  
Review Of The Literature

scholarly journals Gallbladder Agenesis and Cystic Duct Absence in an Adult Patient Diagnosed by Magnetic Resonance Cholangiography: Report of a Case and Review of the Literature

2009 ◽  
Vol 2009 ◽  
pp. 1-4 ◽  
Author(s):  
Valeria Fiaschetti ◽  
Giovanna Calabrese ◽  
Silvia Viarani ◽  
Gabriele Bazzocchi ◽  
Giovanni Simonetti
Keyword(s):  
Congenital Anomaly ◽  
Magnetic Resonance ◽  
Adult Patient ◽  
Biliary Tract ◽  
Cystic Duct ◽  
Congenital Abnormalities ◽  
Review Of The Literature ◽  
Rare Congenital Anomaly ◽  
Biliary Tract Abnormality ◽  
Gallbladder Agenesis

Gallbladder agenesis (GA) is a rare congenital anomaly of the biliary system often associated with other congenital abnormalities. Patients become symptomatic in 23% of cases. GA is often misinterpreted as other diseases, therefore, leading to unnecessary surgery. We report a case of congenital GA associated to cystic duct absence and a biliary tract abnormality diagnosed by Magnetic Resonance with Cholangiopancreatography.

Choledochal Cyst Cholangiocarcinoma Arising from Adenoma: Case Report and a Review of the Literature

2006 ◽  
Vol 63 (4) ◽  
pp. 281-284 ◽  
Author(s):  
Jan Franko ◽  
Michael L. Nussbaum ◽  
Jon B. Morris
Keyword(s):  
Case Report ◽  
Choledochal Cyst ◽  
Review Of The Literature

scholarly journals Primary Pancreatic Burkitt’s Lymphoma: A Case Report and Review of the Literature

2018 ◽  
Vol 2018 ◽  
pp. 1-4 ◽  
Author(s):  
Venkata Rajesh Konjeti ◽  
Gerald M. Hefferman ◽  
Sravanthi Paluri ◽  
Prerna Ganjoo
Keyword(s):  
Case Report ◽  
Obstructive Jaundice ◽  
Clinical Features ◽  
Burkitt Lymphoma ◽  
Pancreatic Head ◽  
Rare Occurrence ◽  
Review Of The Literature ◽  
Rare Presentation ◽  
Pancreatic Lymphoma ◽  
Primary Pancreatic Lymphoma

Primary pancreatic lymphoma (PPL) is of very rare occurrence as an extra nodal site of Non-Hodgkin’s lymphoma (NHL). It represents less than 1% of NHL. Out of which Burkitt lymphoma of pancreas is of a rare presentation. It usually occurs in children and presenting in adults is uncommon. The prevalence of pancreatic Burkitt lymphoma is not known as the incidence is significantly low. Clinical features of PPL are predominantly nonspecific and can become difficult with associated inflammation of pancreas. Differentiation of lymphoma to adenocarcinoma is important as chemotherapy is the main stay of treatment in lymphoma. We report a case of 68-year-old female who presented with nonspecific symptoms and was found to have obstructive jaundice secondary to pancreatic head neoplasm which was proved to be pancreatic Burkitt lymphoma which is a rare presentation.

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
Sign in / Sign up

Export Citation Format

Share Document