Literature DB >> 2689975

Anomalous portal venous connection to the suprahepatic vena cava: sonographic demonstration.

R D Bellah1, J Hayek, R L Teele.   

Abstract

The authors report a congenital portosystemic shunt which was detected with ultrasound in an infant with a fatal congenital hypertrophic cardiomyopathy. An aberration in primitive vitelline venous development may have contributed to the formation of this unusual vessel.

Entities:  

Mesh：

Year:  1989        PMID： 2689975     DOI： 10.1007/bf02010654

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN： 0301-0449


  6 in total

1.  Congenital absence of intrahepatic portal venous system simulating Eck fistula; report of a case with necropsy findings.

Authors:  G HELLWEG
Journal:  AMA Arch Pathol       Date:  1954-05

2.  Congenital absence of the portal vein.

Authors:  D Marois; J A van Heerden; H A Carpenter; P F Sheedy
Journal:  Mayo Clin Proc       Date:  1979-01       Impact factor: 7.616

3.  Congenital absence of portal venous system in a 50-year-old woman.

Authors:  S Olling; R Olsson
Journal:  Acta Med Scand       Date:  1974-10

4.  Developmental basis of the portal venous system.

Authors:  C Marks
Journal:  Am J Surg       Date:  1969-05       Impact factor: 2.565

5.  An unusual portal-systemic shunt, most likely through a patent ductus venosus. A case report.

Authors:  K Ohnishi; H Hatano; T Nakayama; K Kohno; K Okuda
Journal:  Gastroenterology       Date:  1983-10       Impact factor: 22.682

6.  Congenital absence of the portal vein in oculoauriculovertebral dysplasia (Goldenhar syndrome).

Authors:  S S Morse; K J Taylor; E B Strauss; E Ramirez; J H Seashore
Journal:  Pediatr Radiol       Date:  1986
  6 in total
  12 in total

1.  Hypergalactosaemia and portosystemic encephalopathy due to persistence of ductus venosus Arantii.

Authors:  R Gitzelmann; U V Arbenz; U V Willi
Journal:  Eur J Pediatr       Date:  1992-08       Impact factor: 3.183

2.  Congenital absence of the portal vein in a middle-aged man.

Authors:  Flavio Barchetti; Luigi Pellegrino; Najwa Al-Ansari; Valentina De Marco; Paolo Scarpato; Pasquale Ialongo
Journal:  Surg Radiol Anat       Date:  2010-11-23       Impact factor: 1.246

3.  An enormous shunt between the portal and hepatic veins associated with multiple coronary artery fistulas.

Authors:  K Mori; T Dohi; H Yamamoto; M Kamada
Journal:  Pediatr Radiol       Date:  1990

4.  Congenital portosystemic shunts and AMPLATZER vascular plug occlusion in newborns.

Authors:  William N Evans; Alvaro Galindo; Ruben J Acherman; Abraham Rothman; Dean P Berthoty
Journal:  Pediatr Cardiol       Date:  2009-07-23       Impact factor: 1.655

5.  Congenital absence of the portal vein: case report and MR demonstration.

Authors:  J T Laverdiere; T Laor; B Benacerraf
Journal:  Pediatr Radiol       Date:  1995

Review 6.  [Congenital absence of the portal vein (CAPV). Two cases of Abernethy malformation type 1 and review of the literature].

Authors:  K Ringe; E Schirg; M Melter; P Flemming; B Ringe; T Becker; M Galanski
Journal:  Radiologe       Date:  2008-05       Impact factor: 0.635

Review 7.  Congenital extrahepatic portosystemic shunts.

Authors:  Conor P Murray; Shi-Joon Yoo; Paul S Babyn
Journal:  Pediatr Radiol       Date:  2003-07-23

Review 8.  Insight into congenital absence of the portal vein: is it rare?

Authors:  Guo-Hua Hu; Lai-Gen Shen; Jin Yang; Jin-Hua Mei; Yue-Feng Zhu
Journal:  World J Gastroenterol       Date:  2008-10-21       Impact factor: 5.742

9.  Congenital intrahepatic portosystemic venous shunt: sonographic and magnetic resonance imaging.

Authors:  G Santamaría; X Pruna; X Serres; L Inaraja; A Zuasnabar; A Castellote
Journal:  Eur Radiol       Date:  1996       Impact factor: 5.315

10.  Congenital absence of the portal vein associated with focal nodular hyperplasia of the liver and congenital heart disease (Abernethy malformation): A case report and literature review.

Authors:  Yabin Hao; Xu Hong; Xinyan Zhao
Journal:  Oncol Lett       Date:  2014-12-04       Impact factor: 2.967
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.