Results 51 to 60 of about 7,234 (212)
PRENATAL DIAGNOSIS OF NON UROLOGICAL ABDOMINAL CYSTS: A SINGLE CENTRE REPORT OF 100 CONSECUTIVE CASES [PDF]
, 2014 A wide variety of cysts can be detected in the fetal abdomen and does not represent an uncommon finding at routine sonography. Cysts can originate from any intra-abdominal structure, even if most of them belong to the renal tract.
LENZI, ELENA
core
Monolobar Caroli's Disease and cholangiocarcinoma [PDF]
, 2015 Caroli's Disease (CD) is a rare congenital disorder characterized by cystic dilatation of the intrahepatic bile ducts. This report describes a patient with cholangiocarcinoma arising in the setting of monolobar CD.
Abdalla, Eddie +3 more
core +1 more source
Journal of British Surgery, 1995 Abstract Fourteen adults who presented with choledochal cysts were studied. Symptoms in most cases were non-specific, which resulted in delayed diagnosis. Associated extracystic hepatobiliary disease occurred in 11 patients, including two with cholangiocarcinoma.
P M, Hewitt +3 more
openaire +2 more sources
American Journal of Roentgenology, 1980 Ten preoperative cases of choledochal cyst and five patients who had had complications after surgical treatment for their choledochal cysts were studied to evaluate the accuracy of computed tomography (CT) in the diagnosis of this malformation and its complications.
T, Araki, Y, Itai, A, Tasaka
openaire +2 more sources
Type I Choledochal Cyst Complicated With Acute Hemorrhagic Pancreatitis: A Case Report
Journal of Medical Ultrasound, 2017 Choledochal cysts rarely present with acute pancreatitis. We report a patient with type I choledochal cyst(s) who had concomitant acute frank hemorrhagic pancreatitis.
Ping-Hua Tsai +10 more
doaj +1 more source
Congenital choledochal cyst [PDF]
Paediatrica Indonesiana, 1973 Although congenital choledochal cyst, a localized dilatation of the common bile duct, is an unusual condition in many countries, it should be expected in any infant who presents the triad of jaundice, tumor and pain in the right upper abdomen. Not less than 500 cases have been reported in the medical literature.
, Heyder, , Heyder
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Journal of British Surgery, 1974 Abstract This paper reports a series of 8 children with a choledochal cyst. The pathology, diagnosis and treatment of choledochal cyst are discussed. All the cases have been fully followed up and 1 patient has been examined 21 years after operation.
openaire +2 more sources
Simpson-Golabi-Behmel syndrome types I and II [PDF]
, 2014 Simpson-Golabi-Behmel syndrome (SGBS) is a rare overgrowth syndrome clinically characterized by multiple congenital abnormalities, pre/postnatal overgrowth, distinctive craniofacial features, macrocephaly, and organomegaly.
Fernando Santos +6 more
core +1 more source
Diagnostic dilemma in a large choledochal cyst
Journal of Society of Surgeons of Nepal, 2019 Choledochal cysts are rare congenital anomalies that have a variable presentation with occasional diagnostic and therapeutic dilemmas. Our case is a 14-year female presented with recurrent abdomen pain with confusing diagnostic findings, suggestive of
Tul Maya Gurung +2 more
doaj +1 more source
Choledochal cyst: presentation of the disease with a case report.
Biomolecules & Biomedicine, 2011 Choledochal cyst is a rare disease of the biliary tract. There are five main types of choledochal cysts with a few recognized sub-types. The etiology of choledochal cysts still is unclear.
Aleksandar Cvetkovic +2 more
doaj +1 more source