Zobrazeno 1 - 10
of 88
pro vyhledávání: '"todani"'
Autor:
Erick Moreno-Delgado, Adriana A. Soto-Aragón, José A. Sánchez-Sandoval, Edson A. Escandón-Villalobos
Publikováno v:
Revista Médica del Hospital General de México, Vol 87, Iss 91 (2024)
Introduction: Choledochal cysts are a rare congenital anomaly of non-defined etiology, commonly diagnosed in childhood, whose main manifestations are abdominal pain, jaundice, and a palpable mass. Although magnetic resonance cholangiography is the go
Externí odkaz:
https://doaj.org/article/ac5bc26f1bab4e98bcaf1f7071107847
Publikováno v:
Clinical Case Reports, Vol 11, Iss 10, Pp n/a-n/a (2023)
Abstract A choledochal cyst is a rare congenital anomaly of the biliary system, characterized by bile duct cystic dilatation, typically affecting the common bile duct. Choledochal cysts are generally categorized using the Todani classification system
Externí odkaz:
https://doaj.org/article/1b1dfc1bfb424875bdf93c76dcf92efa
Autor:
Deo Justine Hando, Daniel William Kitua, Mbelwa Dennis Bitesigilwe, JohnofGod Leonce Mutajwaha, Mogolodi Gabolwelwe, Hassan Mwinchande Chande, Ally Hamisi Mwanga, Zaitun Mohammed Bokhary, Petronilla Joseph Ngiloi
Publikováno v:
Egyptian Liver Journal, Vol 12, Iss 1, Pp 1-8 (2022)
Abstract Background A choledochal cyst is a relatively rare congenital anomaly of the biliary tree requiring surgery as the definitive treatment. Amongst the five Todani variants, type I poses a diagnostic and treatment challenge owing to its infrequ
Externí odkaz:
https://doaj.org/article/f262dd1df6fd45d8b7aab1d7ecd50ffa
Autor:
Mehak Sehgal, Devendra Kumar Yadav, Devasenathipathy Kandasamy, Minu Bajpai, Vishesh Jain, Anjan Kumar Dhua, Prabudh Goel
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 26, Iss 6, Pp 432-435 (2021)
Choledochal cyst of the cystic duct is a rare anomaly; broadly classified, the pathology may either present as a solitary anomaly or with concomitant involvement of other parts of the biliary tree. In the absence of standard guidelines for surgical p
Externí odkaz:
https://doaj.org/article/4ce1dde5471d4ad29950dc72aa1c0993
Autor:
Adrian Miron, Liliana Gabriela Popa, Elena Adelina Toma, Valentin Calu, Radu Florin Parvuletu, Octavian Enciu
Publikováno v:
Diagnostics, Vol 13, Iss 6, p 1059 (2023)
Choledochal cysts (CCs) are rare occurrences presenting as dilatations of biliary structures, which can present as single or multiple dilatations and can appear as both intra- and extrahepatic anomalies. The most widespread classification of CCs is t
Externí odkaz:
https://doaj.org/article/ca82c808b2054e218eb6db6ba85bf5ce
Publikováno v:
The Egyptian Journal of Radiology and Nuclear Medicine, Vol 51, Iss 1, Pp 1-3 (2020)
Abstract Background Choledochal or common bile duct (CBD) cysts are congenital cystic dilatation of any part of the bile ducts. It has been classified into five main types by Todani et al. Isolated cystic duct cysts are not included in this classific
Externí odkaz:
https://doaj.org/article/cbe429c1f49e4718af3d1ac0e9b02b92
Large choledochal cyst initially interpreted as Mirizzi syndrome - case report and literature review
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 148, Iss 3-4, Pp 216-219 (2020)
Introduction. Choledochal cysts are congenital anomalies manifested as focal or diffuse cystic dilatation of the bile ducts. They are mostly diagnosed in childhood. The magnetic resonance and surgical management are the gold standard diagnostic and t
Externí odkaz:
https://doaj.org/article/80a785cf4b764c7abb9f7542e90ab21e
Autor:
Anneke ten Hove, Ruben H.J. de Kleine, Maarten W. Nijkamp, Annet S.H. Gouw, Timco Koopman, Joost M. Klaase
Publikováno v:
Case Reports in Gastroenterology, Vol 13, Iss 2, Pp 230-237 (2019)
Choledochal malformation (CM) comprise various congenital cystic dilatations of the extrahepatic and/or intrahepatic biliary tree. CM is classified into five different types. Our case describes a 58-year-old man presenting with acute abdominal pain.
Externí odkaz:
https://doaj.org/article/d6b066775c4f4b52af34347111c850ce
Akademický článek
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Publikováno v:
The Pan African Medical Journal, Vol 29, Iss 156 (2018)
La dilatation kystique des voies biliaires (DKVB) est une pathologie rare, elle touche principalement les jeunes femmes, avec la douleur comme maitre symptôme. Son principal risque est la cancérisation. L'exérèse chirurgicale complète demeure le
Externí odkaz:
https://doaj.org/article/ed8a5c2fc44846cdb892bf117a173f4b