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caroli disease/icterícia
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11 resultados
Caroli disease: review of eight cases with emphasis on magnetic resonance imaging features.
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BACKGROUND
Caroli disease is a rare congenital disorder characterized by segmental, nonobstructive dilatation of intrahepatic bile ducts. The term Caroli syndrome is used for the association of Caroli disease with congenital hepatic fibrosis.
OBJECTIVE
To provide an overview of the clinical
[Primary cholangiocarcinoma associated with Caroli disease].
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A 68 years old male presented with right hypochondrium abdominal pain and jaundice with no other clinical finding. CAT Scan and Ultrasonography showed right lobe bile duct dilatation. Magnetic Resonance Cholangiopancreatography gave an outstanding vision of a restricted right lobe bile duct
Type IV choledochal cyst with polycystic kidney disease: a case report
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Background: Choledochal cysts are divided into 5 types. Physicians believe that Caroli disease (which refers to type V biliary cysts) is a special type of biliary cyst caused by a mutation in the PKHD1 gene and is associated with
Choledochal cysts: diagnosis and treatment.
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The aim of this study is to show the different diagnostic procedures and treatment in patients diagnosed with congenital choledochal cysts. Choledochal cysts are congenital anomalies of the bile ducts and include cystic dilatation of the extrahepatic and intrahepatic biliary ducts or both. The study
Unusual cholangiographic findings in a patient with primary sclerosing cholangitis: cystic dilatation.
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A 45-year-old woman with the diagnosis of primary sclerosing cholangitis and ulcerative colitis admitted with the complaints of pruritus and jaundice. Endoscopic retrograde cholangiography revealed entirely narrow, irregular common bile duct and common hepatic duct and unusual cystic dilations in
Renal-hepatic-pancreatic dysplasia: a syndrome reconsidered.
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Five infants, three dying neonatally and two later in the first year of life, had renal, hepatic, and pancreatic dysplasia, a combination of abnormalities first described by Ivemark et al [1959]. The renal malformation consisted of cystic dysplasia, with abnormally differentiated ducts, deficient
Management of choledochal cyst: 30 years of experience and results in a single center.
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BACKGROUND
Choledochal cyst is usually diagnosed in childhood. Early treatment can prevent further complication. We report on our series of patients over the past 30 years.
METHODS
A retrospective study was performed on all pediatric patients who presented with choledochal cyst from January 1978 to
[Congenital cystic disease of the biliary system in adults].
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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
Congenital choledochal cysts in adults.
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OBJECTIVE
Excision of the extrahepatic portion of congenital choledochal cysts (CCs) avoids the risk of cancer. The standard classification scheme is out of date.
METHODS
Retrospective case series and literature review.
METHODS
Tertiary care university hospital.
METHODS
Thirty-eight adult patients
Congenital abnormalities of the pancreas and biliary tree in adults.
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Congenital abnormalities of the pancreaticobiliary tree may go undetected until adulthood. In adult patients with persistent and unexplained signs and symptoms, such as cholangitis, pancreatitis, jaundice, recurrent abdominal pain, and nausea and vomiting, a congenital anomaly of the pancreatic or
Evaluation of Underlying Liver Disease and Its Severity in Children Referred for Liver Transplant: a Single-Center Report From Nemazee Hospital of Shiraz.
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