[1] |
Baiges A, Turon F, Simón‐Talero M, Tasayco S, Bueno J, Zekrini K, et al. Congenital extrahepatic portosystemic shunts (Abernethy malformation): an international observational study. Hepatology. 2019; 71(2):658-69.
doi: 10.1002/hep.30817
|
[2] |
Abernethy J. Account of two instances of uncommon formation in the viscera of the human body: from the philosophical transactions of the royal society of London. Med Facts Obs. 1797; 7:100-8.
|
[3] |
Ponziani FR, Faccia M, Zocco MA, Giannelli V, Pellicelli A, Ettorre GM, et al. Congenital extrahepatic portosystemic shunt: description of four cases and review of the literature. J Ultrasound. 2019; 22(3):349-58.
doi: 10.1007/s40477-018-0329-y
pmid: 30357760
|
[4] |
Sokollik C, Bandsma RH, Gana JC, van den Heuvel M, Ling SC. Congenital portosystemic shunt: characterization of a multisystem disease. J Pediatr Gastroenterol Nutr. 2013; 56(6):675-81.
doi: 10.1097/MPG.0b013e31828b3750
|
[5] |
De Vito C, Tyraskis A, Davenport M, Thompson R, Heaton N, Quaglia A. Histopathology of livers in patients with congenital portosystemic shunts (Abernethy malformation): a case series of 22 patients. Virchows Arch. 2019; 474(1):47-57.
doi: 10.1007/s00428-018-2464-4
|
[6] |
Taydas O, Danisan G, Ogul H, Kantarci M. A rare cause of congenital portosystemic shunt: type 2 Abernethy malformation. Folia Morphol (Warsz). 2020; 79(1):172-5.
|
[7] |
Kiriyama M, Takashima S, Sahara H, Kurosaka Y, Matsushita M, Akiyama T, et al. Case report: portal-systemic encephalopathy due to a congenital extrahepatic portosystemic shunt. J Gastroenterol Hepatol. 1996; 11(7):626-9.
|
[8] |
Raskin NH, Bredesen D, Ehrenfeld WK, Kerlan RK. Periodic confusion caused by congenital extrahepatic portacaval shunt. Neurology. 1984; 34(5):666-9.
pmid: 6538657
|
[9] |
Landau E, Shilo D, Rolnick B, Neuman J. Rare association of progressive congenital extrahepatic portosystemic shunt with development of multifocal hepatocellular carcinoma. BJR Case Rep. 2017; 3(1):20150077.
|
[10] |
Yasukawa R, Akiyama F, Tsukishiro T, Narita I. Chronic portal-systemic shunt encephalopathy in a hemodialysis patient treated with balloon-occluded retrograde transvenous obliteration. Case Rep Nephrol Urol. 2013; 3(1):28-33.
|
[11] |
Vazquez Roque M, Bouras EP.Epidemiology and management of chronic constipation in elderly patients. Clin Interv Aging. 2015; 10:919-30.
|
[12] |
Kerlan RK Jr, Sollenberger RD, Palubinskas AJ, Raskin NH, Callen PW, Ehrenfeld WK. Portal-systemic encephalopathy due to a congenital portocaval shunt. AJR Am J Roentgenol. 1982; 139(5):1013-5.
doi: 10.2214/ajr.139.5.1013
|
[13] |
Sazumi Y, Nishimura Y, Otsuka Y, Mizuta Y, Nakano Y, Sakae H, et al. Hepatic encephalopathy due to extrahepatic portosystemic shunt. Clin Case Rep. 2020; 8:1852-3.
doi: 10.1002/ccr3.2986
|
[14] |
Yang TT, Cheng YY, Deng ZK, Lai YJ. A 73-year-old woman with hyperammonemic encephalopathy caused by noncirrhotic congenital portosystemic shunts. Neurology. 2021; 97(7):340-1.
doi: 10.1212/WNL.0000000000012274
|
[15] |
Merola E, Cao M, La Starza S, Delle Fave MM, Tavanti F, Sergi D, et al. Portosystemic encephalopathy in an 86-year-old patient: a clinical challenge. Acta Gastroenterol Belg. 2016; 79(1):58-9.
|
[16] |
Christou N, Dib N, Chuffart E, Taibi A, Durand-Fontanier S, Valleix D. Stepwise management of hepatocellular carcinoma associated with Abernethy syndrome. Clin Case Rep. 2018; 6(5):930-4.
doi: 10.1002/ccr3.1384
|