Results 61 to 70 of about 5,504 (210)

Choledochal cyst

open access: yesJournal 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

Congenital choledochal cyst in an infant with cystic fibrosis

open access: yesAnnals of Hepatology, 2009
Congenital choledochal cyst is malformation of the biliary ductal system, which rarely occur. We describe here a 4-month old boy, who was referred to our center with respiratory distress and low level consciousness.
Parviz Tabatabaie   +7 more
doaj   +1 more source

A 10-year-old Boy with Giant Choledochal Cyst: A Case Report

open access: yesArchives of Pediatric Gastroenterology, Hepatology, and Nutrition, 2022
Choledochal duct cyst is a rare congenital anomaly in the form of cystic dilatation of both intrahepatic and extrahepatic bile ducts. The clinical symptoms of choledochal cysts are generally due to bile stasis, stone formation, recurrent superinfection,
Ninung RD Kusumawati, Juwita Pratiwi
doaj   +1 more source

The Role of the Multidisciplinary Team in the Management of Complex Cases of Liver Disease in a Peripheral Hospital: A Retrospective Analysis of MDT Registry

open access: yesHealth Science Reports, Volume 9, Issue 3, March 2026.
ABSTRACT Background and Aims In liver disease (LD), multidisciplinary teams (MDTs) support complex decision‐making and may improve care delivery. The present study aims to evaluate the role of a multidisciplinary approach in complex cases of LD in a peripheral hospital. Methods We retrospectively analyzed a prospectively maintained MDT registry.
Gabriele A. Vassallo   +11 more
wiley   +1 more source

Immunohistochemical Study of Choledochal Cyst Wall [PDF]

open access: yes, 2010
Immunohistochemical Study of Choledochal Cyst Wall Introduction. Choledochal cysts are rare congenital anomalies that appear as localized cystic or fusiform biliary tree dilatations.
Arnis Engelis   +5 more
core   +1 more source

Choledochal cysts in adults

open access: yesJournal 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

CT of choledochal cyst [PDF]

open access: yesAmerican 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

Incidence and Mortality Risks of Gastrointestinal Cancers During Working‐Age Period: Trends and Disparities in 204 Countries and Territories (1990–2021)

open access: yesMed Research, Volume 2, Issue 1, Page 58-74, March 2026.
This comprehensive analysis of gastrointestinal (GI) cancer risk reveals that globally, one in 46 people will develop and one in 73 will die from GI cancers during working age (15–64 years), with 2021 incidence and mortality risks of 2.19% and 1.37%, respectively. Key findings demonstrate striking gender disparities, with males facing nearly double the
Yiming Song   +14 more
wiley   +1 more source

Type I Choledochal Cyst Complicated With Acute Hemorrhagic Pancreatitis: A Case Report

open access: yesJournal 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

Severe anaemia secondary to duodenal adenoma in a cat

open access: yesVeterinary Record Case Reports, Volume 14, Issue 1, February 2026.
Abstract A 7‐year‐old female, spayed, domestic shorthair presented with a 24‐hour history of anorexia, lethargy and melaena. The cat was hospitalized and received treatment for hypovolemia, various electrolyte abnormalities and severe anaemia with a blood transfusion, intravenous fluids and medications.
Jocosa Yasenchack   +4 more
wiley   +1 more source

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