Results 31 to 40 of about 7,207 (227)
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 +4 more sources
Adenomyoma of common bile duct arising in a type I choledochal cyst
Indian 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
A Retrospective Surgical Experience Regarding Open and Laparoscopic Procedures of the Hepatic Hydatid Cyst with an up to Date Complete Review of the Literature And a Focus On Original Romanian Techniques [PDF]
, 2016 Introduction: Even though the development of the recent anti-parasitic drugs has led to a high degree of efficiency, surgical treatment still remains the gold standard for a number of conditions. Material and method.
Moldovan, Cosmin Alec +3 more
core +3 more sources
Uncommon Mixed Type I and II Choledochal Cyst: An Indonesian Experience
Case Reports in Surgery, 2013 Bile duct cyst is an uncommon disease worldwide; however, its incidence is remarkably high in Asian population, primarily in children. Nevertheless, the mixed type choledochal cysts are extremely rare especially in adults.
Fransisca J. Siahaya +4 more
doaj +1 more source
Journal 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
Contribution of Imaging in the Diagnosis of Cholangiocarcinoma in Choledochal Cyst
Case 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
The Association of Choledochal Cyst and Pancreatitis: A Case Report and Review of the Literature
Journal of Pediatric Research, 2017 Choledochal cysts are relatively rare congenital anomalies which are characterized by dilatation of the extra-and/or intra-hepatic bile ducts. Pancreatic involvement before choledochal cyst operation might be a risk factor for postoperative pancreatitis.
Yeliz Çağan Appak +4 more
doaj +1 more source
Children, 2020 The concomitant occurrence of duodenal atresia (DA) and a choledochal cyst (CC) has rarely been reported. Knowledge of both the presentation and management of this rare co-occurrence is imperative in avoiding potential complications and sequelae, such as
Brittany Downing +3 more
doaj +1 more source
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken +4 more
wiley +1 more source
Type VI choledochal cyst: A case report
Journal of Marine Medical Society, 2013 Choledochal cysts are rare cystic dilatations of the biliary tree. Most of them are congenital and usually manifest in early childhood but some may manifest later in adult life.
A R Basu +3 more
doaj +1 more source