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congenital absence of common bile duct

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https://www.readbyqxmd.com/read/27279403/congenital-absence-of-the-common-bile-duct-a-rare-anomaly-of-extrahepatic-biliary-tract
#1
Tarun Mittal, Mohan V Pulle, Ashish Dey, Vinod K Malik
Congenital absence of the common bile duct (CBD) is an extremely rare developmental anomaly with right and left hepatic ducts draining directly into the gallbladder (GB). Other synonyms for this clinical condition are "cholecystohepatic ducts", "transverse lie of the GB" or "interposition of the GB". The potential for iatrogenic injury is high, because of either inadvertent division or ligation of the ducts. Diagnosis is mostly made intraoperatively, and needs some form of biliary reconstruction. Herein, we are reporting a case of congenital absence of the CBD in a 36-year-old lady that was detected intraoperatively...
July 2016: Journal of Minimal Access Surgery
https://www.readbyqxmd.com/read/27251812/congenital-absence-of-the-common-bile-duct-a-rare-anomaly-of-extrahepatic-biliary-tract
#2
Tarun Mittal, Mohan V Pulle, Ashish Dey, Vinod K Malik
Congenital absence of the common bile duct (CBD) is an extremely rare developmental anomaly with right and left hepatic ducts draining directly into the gallbladder (GB). Other synonyms for this clinical condition are "cholecystohepatic ducts", "transverse lie of the GB" or "interposition of the GB". The potential for iatrogenic injury is high, because of either inadvertent division or ligation of the ducts. Diagnosis is mostly made intraoperatively, and needs some form of biliary reconstruction. Herein, we are reporting a case of congenital absence of the CBD in a 36-year-old lady that was detected intraoperatively...
April 27, 2016: Journal of Minimal Access Surgery
https://www.readbyqxmd.com/read/22832999/duodenal-duplication-cyst-a-potentially-malignant-disease
#3
B Seeliger, T Piardi, E Marzano, D Mutter, J Marescaux, P Pessaux
BACKGROUND: Duodenal duplication cysts constitute a rare congenital anomaly of the gastrointestinal tract. A recent meta-analysis of the literature between 1999 and 2009 reported a total of 47 cases of duodenal duplication cysts.1 These abnormalities are mostly diagnosed in infancy and childhood. In rare cases, they can remain asymptomatic until adulthood, and 38 % of patients are diagnosed after age 20 years.1 (,) 2 Duodenal duplication cysts are generally benign lesions; nevertheless, three cases of malignant tumours arising inside have been reported...
November 2012: Annals of Surgical Oncology
https://www.readbyqxmd.com/read/21391226/a-classification-of-ductal-plate-malformations-based-on-distinct-pathogenic-mechanisms-of-biliary-dysmorphogenesis
#4
Peggy Raynaud, Joshua Tate, Céline Callens, Sabine Cordi, Patrick Vandersmissen, Rodolphe Carpentier, Christine Sempoux, Olivier Devuyst, Christophe E Pierreux, Pierre Courtoy, Karin Dahan, Katty Delbecque, Sébastien Lepreux, Marco Pontoglio, Lisa M Guay-Woodford, Frédéric P Lemaigre
UNLABELLED: Ductal plate malformations (DPMs) are developmental anomalies considered to result from lack of ductal plate remodeling during bile duct morphogenesis. In mice, bile duct development is initiated by the formation of primitive ductal structures lined by two cell types, namely ductal plate cells and hepatoblasts. During ductal plate remodeling, the primitive ductal structures mature to ducts as a result from differentiation of the ductal plate cells and hepatoblasts to cholangiocytes...
June 2011: Hepatology: Official Journal of the American Association for the Study of Liver Diseases
https://www.readbyqxmd.com/read/20941977/-laparoscopic-approach-in-gallbladder-agenesis-an-intraoperative-surprise
#5
M Beuran, S Păun, I Negoi, R Gănescu, A Runcanu, M Avram, Al L Chiotoroiu
INTRODUCTION: The congenital absence of the gallbladder in the absence of biliary atresia is extremely rare, world literature recognizing only 413 cases. The aim of this study is to clarify the diagnostic and therapeutic approach of this rare condition. METHOD: There were retrospectively analyzed the first 2 cases of gallbladder agenesis admitted and surgically approached in the Emergency Hospital, Bucharest. RESULTS: The first case (woman, 23 years old) had typically biliary complaints at admission, shrinked gallbladder and lithiasis on ultrasound...
July 2010: Chirurgia
https://www.readbyqxmd.com/read/20412506/combined-en-bloc-liver-double-kidney-transplantation-in-an-infant-with-ivc-thrombosis
#6
Margaret M McGuire, Brian A Jones, Melissa A Hull, Meghna V Misra, Charles J Smithers, Neil R Feins, Roger L Jenkins, Craig W Lillehei, William E Harmon, Maureen M Jonas, Heung B Kim
We report a case of a pediatric en bloc liver-double kidney transplant in a patient with IVC thrombosis below the renal veins. The patient is an 11-month-old girl diagnosed with congenital nephrotic syndrome at two months of age. Multifocal liver masses were identified on routine ultrasound at eight months of age. Alpha fetoprotein level was 55 319. Biopsy confirmed hepatoblastoma. CT scan confirmed multiple lesions in both lobes, which would require liver transplantation for resection. She was also found to have thrombosis of her infrarenal IVC secondary to multiple central lines...
November 2011: Pediatric Transplantation
https://www.readbyqxmd.com/read/20318919/observations-on-a-case-of-congenital-absence-of-the-hepatic-and-common-bile-ducts
#7
J B Scriver
No abstract text is available yet for this article.
November 1932: Canadian Medical Association Journal
https://www.readbyqxmd.com/read/18274902/squamous-cell-carcinoma-arising-within-a-choledochal-cyst
#8
REVIEW
Leslie Price, Richard Kozarek, Nicholas Agoff
Choledochal cysts are rare congenital or acquired cystic dilatations of the intra- or extrahepatic bile ducts. Their exact pathophysiology remains unclear. Extensive complications exist with untreated cysts, including biliary stasis and inflammation, with resultant stricture and stone formation, cholangitis, pancreatitis, and malignant degeneration. Most commonly reported malignancies include cholangiocarcinoma, adenocarcinoma, and gallbladder cancer. We report the case of a 41-year-old female with a history of chronic calcific pancreatitis, choledocholithiasis, and a large type I choledochal cyst, who presented with flu-like symptoms followed by painless jaundice and weight loss...
October 2008: Digestive Diseases and Sciences
https://www.readbyqxmd.com/read/17610747/anomalous-opening-of-the-common-bile-duct-into-the-duodenal-bulb-endoscopic-treatment
#9
Selcuk Disibeyaz, Erkan Parlak, Bahattin Cicek, Cem Cengiz, Sedef O Kuran, Dilek Oguz, Hakan Güzel, Burhan Sahin
BACKGROUND: Anomalous biliary opening especially the presence of the ampulla of Vater in the duodenal bulb is a very rare phenomenon. We report clinical implications, laboratory and ERCP findings and also therapeutic approaches in 53 cases. METHODS: The data were collected from the records of 12.158 ERCP. The diagnosis was established as an anomalous opening of the common bile duct (CBD) into the duodenal bulb when there is an orifice observed in the bulb with the absence of a papillary structure at its normal localization and when the CBD is visualized by cholangiography through this orifice without evidence of any other opening...
2007: BMC Gastroenterology
https://www.readbyqxmd.com/read/16979949/biliary-atresia-with-choledochal-cyst-implications-for-classification
#10
REVIEW
Aleixo M Muise, Dan Turner, Eytan Wine, Peter Kim, Margaret Marcon, Simon C Ling
BACKGROUND & AIMS: To illustrate the limitations of the embryonic and perinatal classification system of biliary atresia (BA), we present a child with an antenatal diagnosis of choledochal cyst (CC) associated with BA and review the published literature. METHODS: Medline and Pubmed were searched for "BA and CC," "cystic biliary atresia," "BA and cysts," and "biliary cystic malformations." RESULTS: A 7-week-old with an antenatal diagnosis of CC was found to have BA associated with CC...
November 2006: Clinical Gastroenterology and Hepatology
https://www.readbyqxmd.com/read/16941257/agenesis-of-gallbladder-and-multiple-anomalies-of-the-biliary-tree-in-a-patient-with-portal-thrombosis-a-case-report
#11
Yusuf Bayraktar, H Yasemin Balaban, Serap Arslan, Ferhun Balkanci
A 55-year-old male patient was admitted to hospital because of splenomegaly. Abdominal ultrasonography and computed tomography failed to demonstrate the gallbladder. The diagnosis of right portal vein thrombosis was established by Doppler ultrasonography, splenoportography and computed tomography angiography. To investigate the biliary tree and evaluate the effect on the biliary tree of portal changes, endoscopic retrograde cholangiopancreatography was performed. Endoscopic retrograde cholangiopancreatography study revealed the absence of gallbladder, cystic duct and common bile duct together with the junction of the right and left hepatic ducts at the pancreatic head, with predominant left hepatic duct...
September 2006: Turkish Journal of Gastroenterology: the Official Journal of Turkish Society of Gastroenterology
https://www.readbyqxmd.com/read/15493591/-anomalous-choledocho-pancretic-ductal-junction-in-a-choledochal-cyst-a-case-report
#12
Miodrag Jovanović, Dragoljub Bilanović, Radoje Colović, Nikica Grubor, Milenko Ugljesić
Choledochal cysts are rare congenital anomalies, mostly detected in adults. Pathogenesis of these cysts seems to be in anomalous junction between pancreatic and common bile duct, above the papillary sphincter and outside of the duodenal wall. The absence of the sphincter above the junction is followed by reflux of the pancreatic juice into the bile duct leading to dilatation and fibrous changes of bile duct wall. A 38-year-old female is presented in whom a choledochal cyst was found 11 years earlier, during the operation performed for obstructive jaundice, when cystojejunostomy with Roux-en Y Jejunal limb was carried out...
May 2004: Srpski Arhiv za Celokupno Lekarstvo
https://www.readbyqxmd.com/read/15085989/left-sided-gallbladder-associated-with-congenital-hypoplasia-of-the-left-lobe-of-the-liver-a-case-report-and-review-of-literature
#13
REVIEW
Tomoaki Noritomi, Kenshi Watanabe, Yuichi Yamashita, Shinji Kitagawa, Masao Oshibuchi, Takayuki Shirakusa
Left-sided gallbladder is a rare anomaly that is often associated with other abnormal anatomy in the hepatobiliary system. We report our experience of a case of left-sided gallbladder associated with the congenital hypoplasia of the left lobe of the liver. A 71-year-old woman underwent cholecystectomy for acute cholecystitis. Intraoperative findings revealed the absence of the left lobe of the liver. The gallbladder was located in the left side of the round ligament, which was associated with abnormal intrahepatic portal branching...
January 2004: International Surgery
https://www.readbyqxmd.com/read/14756026/-congenital-cystic-disease-of-the-biliary-system-in-adults
#14
E Târcoveanu, D Niculescu, St Georgescu, Elena Cotea, D Vintilă, G Dimofte, C N Neacşu, C Lupaşcu, Felicia Crumpei, C Cîrdei
Congenital cystic disease of the biliary system is a complex syndrome of ectasies of the intra-, extra- or both situation of biliary tree. This disease has an unsure etiopathogeny. It is uncommon through the third age, with a greater incidence in child, teen-ager and young adult. The goal of our study is to evaluate the symptoms, diagnosis, treatment and histological aspects of the congenital biliary cysts. We performed a retrospective study from March 1988 to July 2003 about 11 patients with this disease treated in our surgical clinic...
October 2003: Revista Medico-chirurgicală̆ a Societă̆ţ̜ii de Medici ş̧i Naturaliş̧ti Din Iaş̧i
https://www.readbyqxmd.com/read/14298642/-note-on-a-case-of-congenital-atresia-of-the-common-bile-duct-and-of-congenital-absence-of-both-radii-in-a-child-with-concomitant-cytomegalic-inclusion-disease
#15
V ANGHELESCU, M GEORGESCU, R CIGHIR, G TIRNOVEANU, G MITESCU
No abstract text is available yet for this article.
January 1964: Revista Medico-chirurgicală̆ a Societă̆ţ̜ii de Medici ş̧i Naturaliş̧ti Din Iaş̧i
https://www.readbyqxmd.com/read/14131992/absence-of-the-cystic-duct
#16
M J SPERLING
No abstract text is available yet for this article.
June 1964: Archives of Surgery
https://www.readbyqxmd.com/read/13999448/congenital-absence-of-the-gallbladder
#17
C H WEDER
No abstract text is available yet for this article.
October 1962: Canadian Journal of Surgery. Journal Canadien de Chirurgie
https://www.readbyqxmd.com/read/13760691/-congenital-absence-of-the-intra-hepatic-bile-ducts
#18
M LELONG, H LETANVIN, D ALAGILLE
No abstract text is available yet for this article.
1960: Acta Medica Academiae Scientiarum Hungaricae
https://www.readbyqxmd.com/read/13419042/congenital-absence-of-the-gall-bladder-with-cystic-dilatation-of-the-common-bile-duct
#19
H F RHEINLANDER, O L BOWENS
No abstract text is available yet for this article.
March 21, 1957: New England Journal of Medicine
https://www.readbyqxmd.com/read/13233440/jaundice-in-mice-due-to-anomalies-of-the-biliary-tract
#20
A M PAPPENHEIMER, F S CHEEVER, H SALK
There has been described a previously unrecognized disease of mice, characterized by progressive jaundice, first appearing during the nursing period. This has been shown to be due to congenital absence of the terminal segment of the common bile duct, or to the absence of intrahepatic ducts. In the former case, there is distension of the cystic and hepatic ducts, and of the gall bladder, with mucoid material. Biliary cirrhosis and infarct-like areas of necrosis are commonly found in the liver. The cause of the necroses has not been positively determined, but it is suggested that they result from defective arteriolization of the hepatic parenchyma...
February 1, 1955: Journal of Experimental Medicine
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