Zobrazeno 1 - 10
of 39
pro vyhledávání: '"abernethy syndrome"'
Publikováno v:
CVIR Endovascular, Vol 5, Iss 1, Pp 1-5 (2022)
Abstract Background Abernethy malformation is a rare condition defined by a congenital extrahepatic portosystemic shunt, often leading to absence or hypoplasia of the intrahepatic portal venous system. Although there are no consensus treatment guidel
Externí odkaz:
https://doaj.org/article/900278eb2900495ab0610d11e6bf1e8d
Publikováno v:
IHJ Cardiovascular Case Reports, Vol 5, Iss 2, Pp 90-93 (2021)
Abernethy syndrome is shunting of blood from portal to systemic circulation resulting in pulmonary vasodilation and ventilation perfusion mismatch.On evaluation of a young male with severe pulmonary hypertension no cause was found. On CECT abdomen ch
Externí odkaz:
https://doaj.org/article/eee10170c11840718eb6707af1a3bdeb
Autor:
N. B. Gubergrits, E. L. Bondar, E. A. Dyadyk, E. V. Berezhnaya, Yu. E. Chirkov, N. V. Byelyayeva, G. M. Lukashevich, T. L. Mozhyna
Publikováno v:
Российский журнал гастроэнтерологии, гепатологии, колопроктологии, Vol 30, Iss 5, Pp 49-57 (2020)
Aim. To present a clinical case of the Abernethy syndrome.Key points. Abernethy syndrome is a rare vascular anomaly associated with a congenital absence of the portal vein, as a result of which portal blood from the intestines and spleen drains direc
Externí odkaz:
https://doaj.org/article/f95f2cd930b04b059d562479cc0df9d2
Autor:
Matevž Harlander, Maja Badovinac, Frosina Markoska, Barbara Salobir, Tomaž Štupnik, Marija Iča Dolenšek, Izidor Kern, Vojka Gorjup, Nazzareno Galiè
Publikováno v:
Pulmonary Circulation, Vol 12, Iss 1, Pp n/a-n/a (2022)
Abstract Congenital extrahepatic portocaval shunt (CEPS) is a rare condition in which a rare congenital vascular anomaly of the portal system is present. CEPS may manifest as pulmonary arterial hypertension (PAH). When diagnosed and treated early, PA
Externí odkaz:
https://doaj.org/article/4838e3bed09d444683f37794fb601ccb
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Objective: The aim of this single-center retrospective study was to analyze the clinical characteristics, treatment options, and course of neonatal-onset congenital portosystemic shunts (CPSS).Methods: We included all patients with CPSS who presented
Externí odkaz:
https://doaj.org/article/d981e654d84c49deb138225c666fb41f
Autor:
Shyam S Kothari
Publikováno v:
Annals of Pediatric Cardiology, Vol 13, Iss 3, Pp 269-271 (2020)
Diffuse pulmonary arteriovenous malformations or pulmonary arterial hypertension (PAH) may result from congenital portosystemic venous shunts. Hemangioma as a physical sign of congenital portosystemic shunts (like Abernethy syndrome) has not been des
Externí odkaz:
https://doaj.org/article/6f906f7ab1914474ab208476eeac8bef
Autor:
Manoj Kumar Sahu, Akshay Kumar Bisoi, Naveen Chandrasekaran Chander, Sandeep Agarwala, Sandeep Chauhan
Publikováno v:
Annals of Pediatric Cardiology, Vol 8, Iss 1, Pp 64-66 (2015)
Abernethy syndrome (congenital extrahepatic portosystemic shunt (CEPS II)) as an etiology of hepatopulmonary syndrome (HPS) is uncommon. The severe hypoxemia and its consequences become incapacitating for the patient. Early shunt closure resolves hyp
Externí odkaz:
https://doaj.org/article/16db7700722a4ac2982e755bb2cc111c
Akademický článek
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Publikováno v:
World Journal of Gastroenterology
Background Abernethy syndrome is a congenital vascular anomaly in which the portal blood completely or partially bypasses the liver through a congenital portosystemic shunt. Although the number of recognized and reported cases is gradually increasing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d33ad6c894d9adf5bc53a4849cea50d2
http://europepmc.org/articles/PMC7545390
http://europepmc.org/articles/PMC7545390
Autor:
Božić, Dorotea, Jukić, Ivana, Majer, Ante, Cambj- Sapunar, Liana, Podrug, Kristian, Ivanović, Tomislav, Šundov, Željko, Puljiz, Željko, Vuković, Jonatan
Introduction: Abernethy syndrome is a rare congenital extrahepatic portosystemic shunt (CEPS) in which splanchnic blood flows straightly into the inferior vena cava (IVC). Compared to type 1, in which the intrahepatic portal tree is not developed, in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::3bb215c0f01bcef3de5ec221aecb841c
https://www.bib.irb.hr/1228284
https://www.bib.irb.hr/1228284
