Results 51 to 60 of about 446,295 (320)

Quistes de colédoco, una causa inusual de ictericia en pediatría. Presentación de serie de casos [PDF]

open access: yes, 2016
ResumenIntroducciónLos quistes de la vía biliar o quistes de colédoco (QC) son una patología rara en nuestro medio. La etiología es desconocida, siendo la hipótesis más aceptada las anomalías en la unión biliopancreática.ObjetivoAnalizar los datos ...
Aguilera Alonso, David   +3 more
core   +1 more source

Pediatric Choledochal Cysts: Unknowns are Decreasing [PDF]

open access: yes, 2019
Choledochal cysts (CCs) are congenital cystic dilatation of extrahepatic and/or intrahepatic bile ducts. CCs are more common in Asian population, the cause is still unknown.
Gezer, Hasan Özkan
core   +1 more source

Pseudopancreatitis and choledochal cyst [PDF]

open access: yesRevista Española de Enfermedades Digestivas, 2004
choledocal cysts (1). Although it is considered a congenital illness, 30% of cases are diagnosed in the adult age. Clinical symptoms are quite variable: the classical triad of abdominal pain, jaundice and abdominal mass is exceptional in adult subjects.
E. Artigues Sánchez de Rojas   +5 more
openaire   +4 more sources

Anomalous choledocho-pancretic ductal junction in a choledochal cyst: A case report [PDF]

open access: yesSrpski Arhiv za Celokupno Lekarstvo, 2004
Choledochal cysts are rare congenital anomalies, mostly detected in adults. Pathogenesis of these cysts seems to be in anomalous junction between pancreatic and common bile duct, above the papillary sphincterand outside of the duodenal wall.
Jovanović Miodrag   +4 more
doaj   +1 more source

Choledochal cyst

open access: yesMymensingh Medical Journal, 2007
Choledochal cyst, a congenital anomaly, is a premalignant condition. Progressive damage to the bile ducts and to the liver parenchyma may also have association with the condition. Subsequent risk of developing cholangiocarcinoma may be lessen by early diagnosis and prompt definitive surgical treatment, that may even permanently correct the condition. A
M A, Gafur, M Z, Rahman
openaire   +2 more sources

Adenomyoma of common bile duct arising in a type I choledochal cyst

open access: yesIndian Journal of Pathology and Microbiology, 2011
Adenomyoma can be misdiagnosed as an adenocarcinoma, leading to needless and extensive surgical resections. A 45-year-old woman presented with right hypochondrial pain. Magnetic resonance imaging showed a choledochal cyst.
Deepak Kumar Singh   +3 more
doaj   +1 more source

Transduodenal resection of a choledochocele (type III choledochal cyst) with sphincteroplasty: A case report [PDF]

open access: yes, 2016
Choledochal cysts are rare congenital anomalies of the biliary tree which may progress to obstruction or malignancy. Of the five Todani variants, choledochocele, or type III choledochal cyst is the rarest.
Dupree, Phylicia   +6 more
core   +2 more sources

Contribution of Imaging in the Diagnosis of Cholangiocarcinoma in Choledochal Cyst

open access: yesCase Reports in Radiology, 2018
The choledochal cyst is a rare congenital malformation of the bile ducts. It is considered as a precancerous state. The incidence of cancer in choledochal cyst increases with age and occurs around 32 years old. Therefore, young adults are often involved.
Djivèdé Witchékpo Maurice Mohamed Akanni   +3 more
doaj   +1 more source

Choledochal Cyst: Their clinical presentation, diagnosis and treatment in central Nepal: a retrospective study

open access: yesJournal of College of Medical Sciences-Nepal, 2017
Background & Objectives: Choledochal cyst is a rare congenital malformation involving the cystic dilatation of intrahepatic and/ or extra-hepatic bile duct.
Sujit Kumar   +2 more
doaj   +1 more source

Automatic segmentation of clear cell renal cell tumors, kidney, and cysts in patients with von Hippel-Lindau syndrome using U-net architecture on magnetic resonance images [PDF]

open access: yesarXiv, 2023
We demonstrate automated segmentation of clear cell renal cell carcinomas (ccRCC), cysts, and surrounding normal kidney parenchyma in patients with von Hippel-Lindau (VHL) syndrome using convolutional neural networks (CNN) on Magnetic Resonance Imaging (MRI). We queried 115 VHL patients and 117 scans (3 patients have two separate scans) with 504 ccRCCs
arxiv  

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