Surgical Treatment of Solitary Neurofibroma of the Common Hepatic Duct: A Rare Cause of Obstructive Jaundice

1995 ◽  
Vol 12 (2) ◽  
pp. 140-143
Author(s):  
Lorenzo Dominioni ◽  
Massimo Bianchi ◽  
Antonio Chiappa ◽  
Renzo Dionigi
Cytopathology ◽  
2020 ◽  
Vol 31 (3) ◽  
pp. 240-242
Author(s):  
Beena U. Ahsan ◽  
Mohamed Alhamar ◽  
Kathryn M. Hogan ◽  
Daniel Schultz ◽  
Tobias Zuchelli ◽  
...  

2020 ◽  
Vol 1 (1) ◽  
Author(s):  
Allah Ditta ◽  
Muhammad Bilal Mirza ◽  
Muhammad Waqas-ur-Rehman ◽  
Maria Fahim ◽  
Farrakh Mehmood Satar ◽  
...  

Background: Congenital biliary web of the extra-hepatic biliary tree is becoming exceedingly rare cause of obstructive jaundice in children. Case Presentation: We report a case of 5-month-old male baby who presented with acholic stools and persistent jaundice since birth. Magnetic resonance cholangiopancreatography (MRCP) showed contracted gall bladder and focal narrowing at mid portion of the common bile duct (CBD) with proximal dilatation of biliary channels. On exploration, a complete web was found just proximal to the confluence of cystic duct and common hepatic duct causing complete obstruction of biliary tree. A Roux-en-Y hepatico-jejunostomy was done. Postoperative recovery was uneventful. Conclusion: We conclude that congenital biliary web is a rare entity and should be considered in the dif­ferential diagnosis of biliary atresia.


1996 ◽  
Vol 10 (2) ◽  
pp. 89-92
Author(s):  
Hugh J Freeman ◽  
Andrew M Seal

A 68-year-old female presented with an enlarged and nontender palpable gallbladder and clinical features of obstructive jaundice. Subsequent laboratory investigations confirmed the presence of cholestasis associated with an obstructing mass in the region of the common hepatic duct. Pathological evaluation of the mass revealed a localized abdominal lymphoma. Treatment with chemotherapy and radiation resulted in complete clinical remission (for almost 14 years at the last evaluation). Primary abdominal lymphoma may involve the hilar region and present as a localized mass. Precise tissue diagnosis is essential to permit an aggressive management approach with the potential for significant clinical benefit.


2019 ◽  
Vol 42 (5) ◽  
pp. 309
Author(s):  
María Curieses Luengo ◽  
Pilar Varela Trastoy ◽  
Aránzazu Álvarez Álvarez

1990 ◽  
Vol 12 (2) ◽  
pp. 207-213 ◽  
Author(s):  
Jonathan Kiev ◽  
David C. Dyslin ◽  
Paul Vitenas ◽  
Morris D. Kerstein

1988 ◽  
Vol 39 (3) ◽  
pp. 201-205 ◽  
Author(s):  
Kwang Choon Lee ◽  
Katsuji Sakai ◽  
Hiroaki Kinoshita ◽  
Kazuhiro Hirohashi ◽  
Yasutoshi Tsuji ◽  
...  

2010 ◽  
Vol 138 (1-2) ◽  
pp. 88-90
Author(s):  
Radoje Colovic ◽  
Nikica Grubor ◽  
Vladimir Radak ◽  
Marjan Micev ◽  
Stojan Latincic

Introduction. Colorectal carcinoma, one of the most frequent carcinomas, produces liver metastasis very frequently. Surprisingly, those secondaries rarely cause obstructive jaundice. If it appears, it is usually caused by compression or infiltration of the major bile ducts close to the hepatic hilus, less frequently with bile duct obstruction by gelatinous mucus produced by the tumour, much rarer by the tumour growth within the, otherwise intact, common bile duct and very rarely by metastasis into the biliary tree. Case Outline. We present a 67-year-old man who had been submitted to left colectomy for sygmoid colon carcinoma four years earlier, now, admitted with an obstructive jaundice, along with a number of liver and lung secondaries. Obstructive jaundice was caused by the vegetative tumour of the proximal part of the common hepatic duct which was resected and anastomosed with a Roux-en-Y jejunal limb. The postoperative recovery was uneventful. The patient died 7 months later without jaundice due to liver and lung secondaries. Histological findings showed cholangiocellular carcinoma of the common hepatic duct, while the histological findings of the liver tumour specimen confirmed metastatic colonic carcinoma. Conclusion. In case of obstructive jaundice in patients with metastatic colonic carcinoma within liver, other aethiological factors of biliary obstruction can not be excluded and have to be taken into differential diagnosis.


HPB Surgery ◽  
1988 ◽  
Vol 1 (1) ◽  
pp. 67-76 ◽  
Author(s):  
Thomas C. Bower ◽  
David M. Nagorney

The Mirizzi syndrome refers to benign obstruction of the common hepatic duct by a stone impacted within the neck or cystic duct of the gallbladder, which causes extrinsic compression of the common hepatic duct and obstructive jaundice. Although a rare cause of obstructive jaundice, it remains a clinically and surgically challenging problem. Five patients with the Mirizzi syndrome were culled from over 9000 patients undergoing operation for gallstone disease. The management of these patients was detailed. Diagnosis requires a high index of clinical suspicion but can be confirmed with the use of ultrasonography and percutaneous transhepatic cholangiography. Cholecystectomy and common duct exploration are essential components of operative therapy, but additional procedures to repair non-circumferential bile duct defects or strictures must be anticipated.


2020 ◽  
pp. 000313482097335
Author(s):  
Rajshri M. Gartland ◽  
Samantha M. Landino ◽  
Norah E. Liang ◽  
Celeste J. Day ◽  
David L. Berger

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