Cystic diseases of the liver and biliary tract

[1]  Ann M. Johnson,et al.  Intracranial aneurysms in autosomal dominant polycystic kidney disease. , 1992, The New England journal of medicine.

[2]  O. Idowu,et al.  Choledochal cyst in Simpson-Golabi-Behmel syndrome. , 1999, American journal of medical genetics.

[3]  D. Geller,et al.  The Changing Presentation of Choledochal Cyst Disease: An Incidental Diagnosis , 2009, HPB surgery : a world journal of hepatic, pancreatic and biliary surgery.

[4]  C. Falk,et al.  Identification of a locus for autosomal dominant polycystic liver disease, on chromosome 19p13.2-13.1. , 2000, American journal of human genetics.

[5]  A. Levy,et al.  Caroli's disease: radiologic spectrum with pathologic correlation. , 2002, AJR. American journal of roentgenology.

[6]  H. Nagai,et al.  Pancreatic Complications in Choledochal Cyst and Their Surgical Outcomes , 2001, World Journal of Surgery.

[7]  J. L. García-Sabrido,et al.  Congenital cystic dilatation of the intrahepatic bile ducts (Caroli's disease): report of a case and review of the literature. , 1979, Surgery.

[8]  J. Bonifacino,et al.  Molecular characterization of hepatocystin, the protein that is defective in autosomal dominant polycystic liver disease. , 2004, Gastroenterology.

[9]  T. Hebiguchi,et al.  Action of pancreatic juice on the bile duct: pathogenesis of congenital choledochal cyst. , 1981, Journal of pediatric surgery.

[10]  P. Gabow,et al.  Autosomal dominant polycystic kidney disease. , 1993, American journal of kidney diseases : the official journal of the National Kidney Foundation.

[11]  A. Toki,et al.  Co‐existing biliary anomalies and anatomical variants in choledochal cyst , 1998, The British journal of surgery.

[12]  C. Scudamore,et al.  Epidemiology, presentation, diagnosis, and outcomes of choledochal cysts in adults in an urban environment. , 2005, American journal of surgery.

[13]  T. J. Brown,et al.  Scintigraphic and radiographic findings in Caroli's disease. , 1984, The American journal of gastroenterology.

[14]  B. Ammori,et al.  Surgical Strategy for Cystic Diseases of the Liver in a Western Hepatobiliary Center , 2002, World Journal of Surgery.

[15]  W. Sumida,et al.  Pancreaticobiliary Maljunction Without Bile Duct Dilatation in Children: Distinction From Choledochal Cyst , 2008, Journal of pediatric gastroenterology and nutrition.

[16]  M. Caplan,et al.  Polycystin-1 C-terminal tail associates with beta-catenin and inhibits canonical Wnt signaling. , 2008, Human Molecular Genetics.

[17]  M. Topazian,et al.  Endoscopic resection of a choledochocele. , 1999, Gastrointestinal endoscopy.

[18]  A. Schepper,et al.  Choledochocele: diagnosis by magnetic resonance imaging , 2000, Abdominal Imaging.

[19]  H. Becker,et al.  Choledochocele: importance of histological evaluation. , 1993, Journal of pediatric surgery.

[20]  I. Murray-Lyon,et al.  Non-communicating multiseptate gall bladder and choledochal cyst: a case report and review of publications. , 1993, Gut.

[21]  P. Lai,et al.  Adult choledochal cyst. , 2005, Asian journal of surgery.

[22]  T. Ochiai,et al.  Risk of bile duct carcinogenesis after excision of extrahepatic bile ducts in pancreaticobiliary maljunction. , 1999, Surgery.

[23]  S. Isaji,et al.  Surgical treatment of type IV choledochal cysts. , 2009, Journal of hepato-biliary-pancreatic surgery.

[24]  C. Chan,et al.  Choledochal cyst: an unusual type of cystic dilatation of the cystic duct. , 1999, AJR. American journal of roentgenology.

[25]  N. Nagasue.  Successful Treatment of Caroli's Disease by Hepatic Resection: Report of Six Patients , 1984, Annals of surgery.

[26]  T. Kajii,et al.  Discordance for anomalous pancreaticobiliary ductal junction and congenital biliary dilatation in a set of monozygotic twins. , 1992, Journal of pediatric surgery.

[27]  A. Irisawa,et al.  Balloon-catheter-assisted complete endoscopic snare resection for choledochocele by using double-channel duodenoscope (with videos). , 2007, Gastrointestinal endoscopy.

[28]  G. Sarris,et al.  Choledochocele: case report, literature review, and a proposed classification. , 1989, Surgery.

[29]  Daniele Marin,et al.  Fibropolycystic liver disease: CT and MR imaging findings. , 2005, Radiographics : a review publication of the Radiological Society of North America, Inc.

[30]  S. Ono,et al.  Long-term outcomes after hepaticojejunostomy for choledochal cyst: a 10- to 27-year follow-up. , 2010, Journal of pediatric surgery.

[31]  Der-Fang Chen,et al.  Choledochal Cysts: Differences Between Pediatric and Adult Patients , 2010, Journal of Gastrointestinal Surgery.

[32]  S. Aoi,et al.  DPC-4 (Smad-4) and K-ras gene mutations in biliary tract epithelium in children with anomalous pancreaticobiliary ductal union. , 2003, Journal of pediatric surgery.

[33]  K. Tyler,et al.  Detection of reovirus RNA in hepatobiliary tissues from patients with extrahepatic biliary atresia and choledochal cysts , 1998, Hepatology.

[34]  H. P. Wang,et al.  Clinical application of EUS and peroral cholangioscopy in a choledochocele with choledocholithiasis. , 1999, Gastrointestinal endoscopy.

[35]  B. Han,et al.  Choledochal cyst: comparison of MR and conventional cholangiography. , 2000, Clinical radiology.

[36]  J. Bonifacino,et al.  Germline mutations in PRKCSH are associated with autosomal dominant polycystic liver disease , 2003, Nature Genetics.

[37]  L. Dorland,et al.  Phosphomannose isomerase deficiency as a cause of congenital hepatic fibrosis and protein-losing enteropathy. , 1999, Journal of hepatology.

[38]  S. Ishihara,et al.  Pancreaticobiliary maljunction and carcinogenesis to biliary and pancreatic malignancy , 2008, Langenbeck's Archives of Surgery.

[39]  R. F. Martín,et al.  Symptomatic choledochoceles in adults. Endoscopic retrograde cholangiopancreatography recognition and management. , 1992, Archives of surgery.

[40]  L. Way,et al.  Congenital choledochal cysts in adults. , 2004, Archives of surgery.

[41]  H. Pitt,et al.  Choledochal cysts in western adults: Complexities compared to children , 2004, Journal of Gastrointestinal Surgery.

[42]  V. Desmet.  Pathogenesis of Ductal Plate Abnormalities , 1998 .

[43]  P. Gabow,et al.  Hereditary and acquired cystic disease of the kidney. , 1994, Kidney international.

[44]  G. Maddern,et al.  Management dilemmas with choledochal cysts. , 2003, Archives of surgery.

[45]  Qiu-Shi Wang,et al.  Choledochal cysts in pregnancy: case management and literature review. , 2004, World journal of gastroenterology.

[46]  M. V. van Oijen,et al.  Lanreotide reduces the volume of polycystic liver: a randomized, double-blind, placebo-controlled trial. , 2009, Gastroenterology.

[47]  L. Antiga,et al.  Reducing polycystic liver volume in ADPKD: effects of somatostatin analogue octreotide. , 2010, Clinical journal of the American Society of Nephrology : CJASN.

[48]  M. Dayton,et al.  Caroli's Disease: a premalignant condition? , 1983, American journal of surgery.

[49]  M. Choti,et al.  Choledochal cyst disease in children and adults: a 30-year single-institution experience. , 2008, Journal of the American College of Surgeons.

[50]  V. Desmet.  Ludwig symposium on biliary disorders--part I. Pathogenesis of ductal plate abnormalities. , 1998, Mayo Clinic proceedings.

[51]  V. Kirimlioğlu,et al.  CASE REPORT: Choledochal Cyst Spontaneously Rupturing the Hepatic Artery , 2000, Digestive Diseases and Sciences.

[52]  S. Song,et al.  Normal structure, variations, and anomalies of the pancreaticobiliary ducts of Koreans: a nationwide cooperative prospective study. , 2002, Gastrointestinal endoscopy.

[53]  V. Garrigues,et al.  Endoscopic biliary manometry in patients with suspected sphincter of Oddi dysfunction and in patients with cystic dilatation of the bile ducts , 1989, Digestive Diseases and Sciences.

[54]  Ann M. Johnson,et al.  Risk factors for the development of hepatic cysts in autosomal dominant polycystic kidney disease , 1990, Hepatology.

[55]  J. Bonifacino,et al.  Polycystic liver disease is a disorder of cotranslational protein processing. , 2005, Trends in molecular medicine.

[56]  I. Pinto,et al.  Intestinal intussusception as a presenting feature of choledochocele , 2005, Gastrointestinal Radiology.

[57]  G. Everson.  Hepatic cysts in autosomal dominant polycystic kidney disease. , 1990, American journal of kidney diseases : the official journal of the National Kidney Foundation.

[58]  M. Bhutani,et al.  EUS findings of 2 large enteric submucosal masses in a patient with choledochocele. , 2006, Gastrointestinal endoscopy.

[59]  E. D. de Lange,et al.  Choledochocele: a rare form of choledochal cyst. , 1988, Southern medical journal.

[60]  A. Yamataka,et al.  Forme fruste choledochal cyst: long-term follow-up with special reference to surgical technique. , 2003, Journal of pediatric surgery.

[61]  H. Pitt,et al.  Choledochal Cyst Disease A Changing Pattern of Presentation , 1994, Annals of surgery.

[62]  T. Okai,et al.  Biliary papillomatosis with the point mutation of K-ras gene arising in congenital choledochal cyst. , 1993, Gastroenterology.

[63]  N. LaRusso,et al.  Cholangiociliopathies: genetics, molecular mechanisms and potential therapies , 2009, Current opinion in gastroenterology.

[64]  S. Sherlock,et al.  Hepatobiliary fibropolycystic diseases. A clinical and histological review of 51 patients. , 1986, Journal of hepatology.

[65]  J. Noseworthy,et al.  Neonatal Cholestatic Conditions Requiring Surgical Reconstruction , 1987, Seminars in liver disease.

[66]  D. Foo,et al.  Impact of prenatal diagnosis on choledochal cysts and the benefits of early excision , 2009, Journal of paediatrics and child health.

[67]  E. M. Barker,et al.  Caroli's disease: Successful management using permanent‐access hepaticojejunostomy , 1985, The British journal of surgery.

[68]  J. Mössner,et al.  Caroli's disease: liver resection and liver transplantation. Experience in 33 patients. , 2005, Surgery.

[69]  D. Bigam,et al.  Polycystic Liver Disease: Experience at a Teaching Hospital , 2005, The American Journal of Gastroenterology.

[70]  Yasunori Sato,et al.  Activation of the MEK5/ERK5 cascade is responsible for biliary dysgenesis in a rat model of Caroli's disease. , 2005, The American journal of pathology.

[71]  K. Davies,et al.  A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16 , 1985, Nature.

[72]  P. Karhunen,et al.  Adult polycystic liver and kidney diseases are separate entities , 1986, Clinical genetics.

[73]  Y. Nakanuma,et al.  Polycystic kidney rat is a novel animal model of Caroli's disease associated with congenital hepatic fibrosis. , 2001, The American journal of pathology.

[74]  W. T. Foulk.  Congenital malformations of the intrahepatic biliary tree in the adult. , 1970, Gastroenterology.

[75]  A. Yamataka,et al.  Cholecystectomy alone is inadequate for treating forme fruste choledochal cyst: evidence from a rare but important case report , 2004, Pediatric Surgery International.

[76]  K. Okajima,et al.  Congenital bile duct cysts: Classification, operative procedures, and review of thirty-seven cases including cancer arising from choledochal cyst. , 1977, American journal of surgery.

[77]  A. Toki,et al.  Classification of congenital biliary cystic disease: special reference to type Ic and IVA cysts with primary ductal stricture. , 2003, Journal of hepato-biliary-pancreatic surgery.

[78]  M. Yamaguchi.  Congenital choledochal cyst. Analysis of 1,433 patients in the Japanese literature. , 1980, American journal of surgery.

[79]  J. M. van de Kamp,et al.  Abnormal hepatocystin caused by truncating PRKCSH mutations leads to autosomal dominant polycystic liver disease , 2004, Hepatology.

[80]  M. Naga,et al.  Endoscopic management of choledochal cyst. , 2004, Gastrointestinal endoscopy.

[81]  L. Spitz.  Experimental production of cystic dilatation of the common bile duct in neonatal lambs. , 1977, Journal of pediatric surgery.

[82]  G. Everson,et al.  Polycystic disease of the liver , 2004, Hepatology.

[83]  A. Yamataka,et al.  Different types of congenital biliary dilatation in dizygotic twins , 1999, Pediatric Surgery International.

[84]  K. Lillemoe,et al.  Choledochoceles: Are They Choledochal Cysts? , 2010, Annals of surgery.

[85]  M. Bertagnolli,et al.  Choledochal cysts in adults: a report of two cases and review of the literature. , 1998, The American journal of gastroenterology.

[86]  A. F. S. Serradel,et al.  Cystic dilatation of the cystic duct: a new type of biliary cyst. , 1991, Surgery.

[87]  P. Pandolfi,et al.  Polycystin-1 Regulates Extracellular Signal-Regulated Kinase-Dependent Phosphorylation of Tuberin To Control Cell Size through mTOR and Its Downstream Effectors S6K and 4EBP1 , 2009, Molecular and Cellular Biology.

[88]  E. Coto,et al.  Comparison of phenotypes of polycystic kidney disease types 1 and 2 , 1999, The Lancet.

[89]  P. Ros,et al.  Hepatic Bile Duct Hamartomas (von Meyenburg Complexes): MR and MR Cholangiography Findings , 2002, Journal of computer assisted tomography.

[90]  S. Kim.  Choledochal cyst: survey by the surgical section of the American Academy of Pediatrics. , 1981, Journal of pediatric surgery.

[91]  N. Shaheen,et al.  TYPE I CHOLEDOCHAL CYST IN ASSOCIATION WITH FAMILIAL ADENOMATOUS POLYPOSIS , 1998, American Journal of Gastroenterology.

[92]  F. J. Brunton,et al.  Intraluminal diverticulum of the duodenum and choledochocele , 1972, Gut.

[93]  Y. Mao,et al.  Expression of matrix metalloproteinase 1 and 2 in congenital choledochal cyst and its clinical significance , 2008, World journal of pediatrics : WJP.

[94]  R. Kozarek,et al.  Squamous Cell Carcinoma Arising Within a Choledochal Cyst , 2008, Digestive Diseases and Sciences.

[95]  E. Bradley,et al.  Cholangiocarcinoma developing after simple excision of a type II choledochal cyst. , 1992, Southern medical journal.

[96]  H. Won,et al.  Can MRCP replace the diagnostic role of ERCP for patients with choledochal cysts? , 2005, Gastrointestinal endoscopy.

[97]  Hyun-Young Kim,et al.  Is excision of a choledochal cyst in the neonatal period necessary? , 2006, Journal of pediatric surgery.

[98]  G. Imvrios,et al.  Monolobar Caroli's disease complicated by cholangiocarcinoma in a 70-year-old man, previously asymptomatic. , 2004, Gastrointestinal endoscopy.

[99]  Po-Huang Lee,et al.  Clinicopathological Feature and Surgical Outcome of Choledochal Cyst in Different Age Groups: The Implication of Surgical Timing , 2008, Journal of Gastrointestinal Surgery.

[100]  H. Bismuth,et al.  Choledochal cystic malignancies. , 1999, Annals of oncology : official journal of the European Society for Medical Oncology.

[101]  M. Kapan,et al.  Choledochal cysts in adults and the importance of differential diagnosis. , 2002, Journal of hepato-biliary-pancreatic surgery.

[102]  R. Weiss,et al.  Obstructing choledochocele: diagnosis by endoscopic ultrasound , 2004, Abdominal Imaging.

[103]  K. Lewin,et al.  Massive hepatomegaly in adult polycystic liver disease. , 1988, The American journal of surgical pathology.

[104]  K. V. van Erpecum,et al.  Highly symptomatic adult polycystic disease of the liver. A report of fifteen cases. , 1987, Journal of hepatology.

[105]  S. Somlo,et al.  Secondary and tertiary structure modeling reveals effects of novel mutations in polycystic liver disease genes PRKCSH and SEC63 , 2010, Clinical genetics.

[106]  E. Lebenthal,et al.  Development of functional responses in human exocrine pancreas. , 1980, Pediatrics.

[107]  P. Kamath,et al.  Clinical profile of autosomal dominant polycystic liver disease , 2003, Hepatology.

[108]  F. Nakayama,et al.  Increased lysophosphatidylcholine and pancreatic enzyme content in bile of patients with anomalous pancreaticobiliary ductal junction , 1991, Hepatology.

[109]  J. Caroli.  Diseases of the intrahepatic biliary tree. , 1973, Clinics in gastroenterology.

[110]  James Glockner,et al.  Randomized clinical trial of long-acting somatostatin for autosomal dominant polycystic kidney and liver disease. , 2010, Journal of the American Society of Nephrology : JASN.