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Choledocal cyst

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https://www.readbyqxmd.com/read/27919528/laparoscopic-approach-to-the-treatment-of-type-ii-choledocal-cysts
#1
Aylhin López-Marcano, Roberto de la Plaza-Llamas, José Manuel Ramia, Farah Al-Shwely, Jhonny Gonzales-Aguilar, Anibal Medina Velasco
No abstract text is available yet for this article.
December 2, 2016: Gastroenterología y Hepatología
https://www.readbyqxmd.com/read/27215168/choledochal-cysts-in-pregnancy-a-case-report-and-literature-review
#2
Annunziata Panebianco, Giuseppe Carbotta, Antonio Prestera, Rita Laforgia, Annalisa Volpi, Pierluca Sallustio
AIM: Aim is to demonstrate that surgery can be the best way to reduce the risk of malignancy in choledochal cysts (CC) and how hard can be the diagnosis and the treatment during pregnancy. CASE REPORT: We report a case of a pregnant young woman (36 week) with a Todani's score II CC. After caesarean, due to increasing jaundice, she underwent magnetic resonance cholangiopancreatography (MRCP) and Endoscopic retrograde cholangiopancreatography (ERCP) that confirmed the diagnosis...
2016: Annali Italiani di Chirurgia
https://www.readbyqxmd.com/read/26994400/significance-of-imaging-modalities-for-preoperative-evaluation-of-the-pancreaticobiliary-system-in-surgery-for-pediatric-choledochal-cyst
#3
Takeshi Saito, Keita Terui, Tetsuya Mitsunaga, Mitsuyuki Nakata, Hideo Yoshida
OBJECTIVE: Roles of magnetic resonance cholangiopancreatography (MRCP), endoscopic retrograde cholangiopancreatography (ERCP), drip infusion cholangiography with computed tomography (DIC-CT), and intraoperative cholangiopancreatography (IOCP) in visualizing pancreaticobiliary anatomy for pediatric choledocal cyst (CC) operations were examined. METHODS: From 1980-2013, 117 pediatric CC patients (median age, 3 years) underwent hepaticojejunostomy at our institution, with imaging modalities of ERCP (n = 81 over 34 years), MRCP, DIC-CT, and IOCP (n = 45, 20, and 45 cases over the last 12 years)...
June 2016: Journal of Hepato-biliary-pancreatic Sciences
https://www.readbyqxmd.com/read/26228985/-acute-pancreatitis-in-childhood-by-choledocal-stone-in-a-choledocal-cyst-case-report
#4
Tayana Bedregal-Mendoza, Irma A Matos-Rojas, Jacpar E Díaz Gonzales, Raúl Ramírez-De la Cruz, Rosa Castro-Johanson
Acute pancreatitis is a known complication of choledochal cysts. It is associated with changes in the biliopancreatic junction and with intra-cystic gallstones. We describe a case of pancreatitis and biliary obstruction caused by choledochal cyst type IVa complicated with obstruction by biliary stones in a 2 year old infant.
April 2015: Revista de Gastroenterología del Perú: órgano Oficial de la Sociedad de Gastroenterología del Perú
https://www.readbyqxmd.com/read/25630013/laparoscopy-assisted-transjejunal-endoscopic-retrograde-cholangiography-for-treatment-of-intrahepatic-duct-stones-in-a-post-roux-en-y-patient
#5
Salah M Mansor, Salem I Abdalla, Rashed S Bendardaf
We report a case of a 17-year-old female patient, who was operated on for choledocal cyst with Roux-en Y hepatojejunostomy. She was admitted to hospital with recurrent attacks of acute ascending cholangitis due to left intrahepatic duct stones. After a failed attempt at conventional endoscopic retrograde cholangiopancreatography through the anatomical route, she was treated successfully with laparoscopy assisted transjejunal endoscopic retrograde cholangiography. 
January 2015: Saudi Medical Journal
https://www.readbyqxmd.com/read/25600242/choledochal-cyst-mimicking-mirizzi-s-syndrome-a-case-report
#6
Fabrizio Maria Frattaroli, Saverio Coiro, Aldo Nunziale, Francesco De Lucia, Jacopo Maria Frattaroli, Giuseppe Pappalardo
Choledochal cysts are cystic dilatations of the intra or extra-hepatic biliary tract with an incidence of 1 case per 150.000 live births. Cysts usually are diagnosed in childhood, but diagnosis can be delayed until adulthood in the 20-50% of cases. Clinical manifestations comprise abdominal pain with biliary or pancreatic features. Mirizzi's syndrome is a late and rare complication, that occurs in 1% of patients with cholelithiasis due to extrinsic compression of the common bile duct by stones impacted either in the gallbladder or in the cystic duct...
September 2014: Annali Italiani di Chirurgia
https://www.readbyqxmd.com/read/25336283/choledochal-cyst-mimicking-mirizzi-s-syndrome-a-case-report
#7
Fabrizio Maria Frattaroli, Saverio Coiro, Aldo Nunziale, Francesco De Lucia, Jacopo Maria Frattaroli, Giuseppe Pappalardo
Choledochal cysts are cystic dilatations of the intra or extra-hepatic biliary tract with an incidence of 1 case per 150.000 live births. Cysts usually are diagnosed in childhood, but diagnosis can be delayed until adulthood in the 20-50% of cases. Clinical manifestations comprise abdominal pain with biliary or pancreatic features. Mirizzi's syndrome is a late and rare complication, that occurs in 1% of patients with cholelithiasis due to extrinsic compression of the common bile duct by stones impacted either in the gallbladder or in the cystic duct...
2014: Annali Italiani di Chirurgia
https://www.readbyqxmd.com/read/24330383/massive-congenital-choledocal-cyst
#8
Lauren E Tracy, David K Imagawa
No abstract text is available yet for this article.
July 2014: Liver International: Official Journal of the International Association for the Study of the Liver
https://www.readbyqxmd.com/read/23833923/-acute-pancreatitis-in-children
#9
O Gómez Beltrán, L Roldán Molleja, J I Garrido Pérez, M Medina Martínez, R Granero Cendón, R González de Caldas Marchal, M Rodríguez Salas, J Gilbert Pérez, R M Paredes Esteban
INTRODUCTION: Lately, there has been an increase in incidence of acute pancreatitis in childhood. Fortunately, 80% of cases are mild and do not require surgical approach. Several etiologic factors have been implicated, such as infections, trauma, congenital anomalies, drugs, biliary diseases. The aim of this study was to assess etiology, clinical features and outcomes of children with acute pancreatitis treated at our center. MATERIALS AND METHODS: A retrospective chart review of our cases of acute pancreatitis in patients younger than 16 years old was performed...
January 2013: Cirugía Pediátrica: Organo Oficial de la Sociedad Española de Cirugía Pediátrica
https://www.readbyqxmd.com/read/23701774/does-an-isolated-benign-choledochal-stricture-hide-a-psc
#10
Paola De Angelis, Renato Tambucci, Erminia Romeo, Francesca Rea, Claudia Caloisi, Tamara Caldaro, Giovanni Federici di Abriola, Francesca Foschia, Filippo Torroni, L Monti, Luigi Dall'Oglio
BACKGROUND: Strictures of the extra-hepatic biliary tree are rare in children and have a benign non-traumatic inflammatory origin or are related to idiopathic fibrosing pancreatitis. Primary sclerosing cholangitis (PSC) can manifest as multiple biliary strictures or as a single dominant stricture. We describe the presentation, treatment, and outcome of six cases of isolated benign choledochal stricture (IBCS). METHODS: All patients underwent magnetic resonance cholangiography (MRC)...
May 2013: Journal of Pediatric Surgery
https://www.readbyqxmd.com/read/23596735/-prenatal-diagnosis-of-choledochal-cyst
#11
Ricardo Jorge Hernández Herrera, Roberto Flores Santos, Adán Hinojosa Salinas, René Ramos González, Beatriz Ramírez González
The choledocal cyst is a defect of the biliary extrahepatic route, the incidence is 1 in 100-150,000 newborns. This paper reports the case of a female newborn with choledocal cyst detected prenatally, from a 32-year-old mother, 2nd term pregnancy, who was diagnosed in the routine obstetric ultrasound as an abdominal fetal cyst. An anatomic obstetric ultrasound confirmed the diagnosis that was defined of a probable hepatic origin. Newborn was delivered at 39 weeks by caesarean section, with weight of 3,980 g and Apgar score 9-9 in conventional time...
February 2013: Ginecología y Obstetricia de México
https://www.readbyqxmd.com/read/22104483/-cholelithiasis-in-infants-children-and-adolescents
#12
REVIEW
Dominique Debray, Stéphanie Franchi-Abella, Sabine Irtan, Muriel Girard
The prevalence of cholelithiasis is estimated within 0.13% and 2% of children under 19 years of age. Pigment stones are the commonest type of gallstones in children, without recognizable predisposing factors in infants or secondary to a predisposing disease such as chronic hemolysis and ileal disease in children. In adolescents, idiopathic cholesterol gallstones accounts for the majority, such as in adults. Gallbladder stones are found in 80 to 90% of cases and common bile duct stones in 10 to 20% of cases...
May 2012: La Presse Médicale
https://www.readbyqxmd.com/read/21797955/favorable-outcome-of-primary-liver-transplantation-in-children-with-cirrhosis-and-hepatocellular-carcinoma
#13
Fabrizio Romano, Paola Stroppa, Michela Bravi, Valeria Casotti, Alessandro Lucianetti, Michela Guizzetti, Aurelio Sonzogni, Michele Colledan, Lorenzo D'Antiga
The outcome of HCC after transplantation (OLT) in children is not well known. Unfavorable features based on adult reports may lead to contraindicate OLT even in children. We reviewed a cohort of children with cirrhosis and HCC to evaluate their outcome after primary transplantation. We considered children with cirrhosis and HCC who had a primary OLT. We retrospectively recorded demographic, medical and surgical features, and MC as predictors of outcome. Among 456 children transplanted in the last 15 yr, 10 (2%), median age at diagnosis 1...
September 2011: Pediatric Transplantation
https://www.readbyqxmd.com/read/21312068/pancreatoduodenal-junction-review-of-anatomy-and-pathologic-conditions
#14
REVIEW
Diana Hernandez-Jover, Juan Carlos Pernas, Silvia Gonzalez-Ceballos, Ion Lupu, Josep Maria Monill, Carmen Pérez
INTRODUCTION: The pancreatoduodenal junction is a small anatomic area where pathologic processes involving the distal bile duct, duodenum, pancreatic head, ampulla de Vater, and retroperitoneum converge. Differential diagnosis includes a spectrum of entities that ranges from anatomical variants to malignancies. PURPOSE: The aim of this paper was to review the anatomy and different pathologic conditions, whether tumoral, inflammatory, or congenital in origin, in this specific area that involves the pancreatic head, duodenum, duodenal ampulla, distal pancreatobiliary tract junction, and retroperitoneum...
July 2011: Journal of Gastrointestinal Surgery: Official Journal of the Society for Surgery of the Alimentary Tract
https://www.readbyqxmd.com/read/18254302/-epidemiological-etiological-and-evolutionary-aspects-of-children-cirrhosis-in-a-developing-country-experience-of-the-pediatric-department-of-sfax-university-hospital-tunisia
#15
Malek Chaabouni, Sonia Bahloul, Wafa Ben Romdhane, Mounir Ben Saleh, Nabil Ben Halima, Chokri Chouchene, Amel Ben Hmad, Nafissa Zroud, Thouraya Kammoun, Abderrahmen Karray
BACKGROUND: Cirrhosis is rare in pediatrics. The children cirrhosis is particular by the ascendancy of biliairy cirrhosis and cirrhosis due to an innate error of metabolism and by the relative frequency of the cases where an etiological treatment is possible. However in developing countries, the children cirrhosis still put problems of etiological diagnosis and of therapeutic coverage. AIM: To study epidemiological and etiological particularities, therapeutic modalities and outcome of cirrhosis in the south of Tunisia...
September 2007: La Tunisie Médicale
https://www.readbyqxmd.com/read/17632995/-congenital-choledocal-cyst-of-adult-report-of-two-cases
#16
O Ka, M Dieng, I Konate, P A Ba, S Ndongo, M Mbengue, A Pouye, A Leye, E H Niang, A Dia, C T Toure
INTRODUCTION: Congenital choledochal cyst is a congenital dilatation of the biliary tract often associated with a long common bilio-pancreatic duct without obstruction. PATIENTS AND METHOD: We report the case of two women who presented a congenital choledochal cyst. RESULTS: For the first patient, the diagnosis was effected during a laparoscopic cholecystectomy for a gall bladder lithiasis. The second one presented repeted access of angiocholitis...
2005: Dakar Médical
https://www.readbyqxmd.com/read/17185973/-an-exceptional-and-misleading-case-of-choledochal-cyst
#17
Alessio Carloni, Ibrahim Dagher, Fabienne Beuzen, Anne Dumas-De La Roque, Dominique Franco
The authors report a case of choledocal cyst extended to left and right hepatic ducts. An heterogeneous intracystic fluid, partial calcification of cystic wall, a slight positivity of echinoccosis serology in a patient from a highly endemic country erroneously led to diagnosis of hydatid cyst invading the left hepatic duct. The diagnosis of choledocal cyst was done on the resection specimen after left hepatectomy. A small patch of cyst wall with terminations of both right sectorial hepatic ducts was used for cysto-jejunal Roux-en-Y loop anastomosis...
November 2006: Gastroentérologie Clinique et Biologique
https://www.readbyqxmd.com/read/16671510/-choledocal-cyst-analysis-of-29-cases-and-review-or-the-literature
#18
REVIEW
J J Vila-Carbó, L Ayuso, E Hernández, J Lluna, V Ibáñez
UNLABELLED: The aim of the present study has been to systematize the clinical presentation of the entity named choledochal cyst, in relation with its probable etiopathology and the intraoperative findings as well as its evolution after surgery, based on the revision of the literature and of our experience in 29 cases. MATERIAL AND METHODS: 29 cases of cystic dilatation of the biliar duct extra and/or intrahepatic are analyzed. In 4 cases the diagnosis was prenatal and two were excluded of the study after it has been confirmed they suffered biliary atresia type I...
January 2006: Cirugía Pediátrica: Organo Oficial de la Sociedad Española de Cirugía Pediátrica
https://www.readbyqxmd.com/read/15179833/intrahepatic-cystadenocarcinoma-with-pleural-dissemination-a-case-report
#19
Seikan Hai, Kazuhiro Hirohashi, Takatsugu Yamamoto, Takahiro Uenishi, Shoji Kubo, Hiromu Tanaka, Taichi Shuto, Shogo Tanaka, Masao Ogawa, Hiroaki Kinoshita
A 40-year-old Japanese woman, who previously had undergone choledocho-jejunostomy in childhood for a congenital choledocal cyst, presented with right-sided chest pain. Computed tomography and ultrasonography demonstrated a right pleural effusion and a 10-cm unilocular hepatic cystic lesion with no solid component. These findings suggested a non-neoplastic cyst or cystadenoma. However, intracystic fluid aspirated had high concentrations of carbohydrate antigen 19-9 and carcinoembryonic antigen. Cytology of the pleural effusion demonstrated malignant cells...
December 2003: Osaka City Medical Journal
https://www.readbyqxmd.com/read/15069627/mucinous-cystadenoma-of-the-pancreas-17-years-after-excision-of-gallbladder-because-of-a-choledochal-cyst
#20
REVIEW
Takuma Tajiri, Genshu Tate, Tomoko Inagaki, Toshiaki Kunimura, Kazuaki Inoue, Toshiyuki Mitsuya, Makoto Yoshiba, Toshio Morohoshi
A 56-year-old woman who had undergone excision of the gallbladder because of a choledochal cyst had a tumorous lesion of the pancreas identified by upper abdominal ultrasonography, but an operation was not carried out, because there was no apparent increase in the cystic mass and no elevation of serum tumor markers. In October 2001, she was admitted to our hospital to check for malignancy because of elevated levels of the tumor marker Dupan-2. Abdominal enhanced computed tomography and upper abdominal ultrasonography revealed a large multilocular cystic mass in the body to tail of the pancreas...
2004: Journal of Gastroenterology
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