scholarly journals Systemic-to-pulmonary venous shunt in a hemodialysis patient with extensive thrombosis of superior and inferior vena cava

Author(s):  
Eduardo O. Valle ◽  
Lorena C. Mainardes ◽  
Marcio dos Santos Meira ◽  
Murilo Henrique Dela Páscoa Toranzo ◽  
Rosilene M. Elias
1997 ◽  
Vol 70 (832) ◽  
pp. 418-420 ◽  
Author(s):  
M Kanematsu ◽  
H Hoshi ◽  
T Imaeda ◽  
S Mizuno ◽  
R Yokoyama

2017 ◽  
Vol 51 (1) ◽  
pp. 38-42 ◽  
Author(s):  
Hilal Sahin ◽  
Yeliz Pekcevik ◽  
Ramazan Aslaner

The duplication of the inferior vena cava (IVC) is a rare congenital anomaly, which also has some variations regarding the complex embryological development of the IVC. In the typical form, infrarenal IVC segments are duplicated and the left IVC joins the left renal vein, which crosses anterior to the aorta in the normal fashion to join the right IVC. In variant forms, the interruption of the intrahepatic segment of the IVC, azygos or hemiazygos continuation, or retroaortic course of the renal vein may be seen. An intrahepatic venous shunt accompanying a double IVC variant is an extremely rare anomaly. We report a case of 40-year-old female patient with double IVC, hemiazygos continuation, intrahepatic IVC interruption, and a transhepatic venous shunt.


2006 ◽  
Vol 175 (4S) ◽  
pp. 392-393
Author(s):  
Fernando P. Secin ◽  
Zohar A. Dotari ◽  
Bobby Shayegan ◽  
Semra Olgac ◽  
Bertrand Guillonneau ◽  
...  

VASA ◽  
1999 ◽  
Vol 28 (4) ◽  
pp. 289-292 ◽  
Author(s):  
Tiesenhausen ◽  
Amann ◽  
Thalhammer ◽  
Aschauer

Congenital anomalies of the caval vein are often associated with other abnormities such as heart defects, situs inversus or a polysplenia-asplenia-syndrome. An isolated, congenital malformation like aplasia of the inferior vena cava is a rare finding. A review of the embryology and abnormities, diagnostics, clinical signs and treatment is given together with the histories of two patients having thrombosis of the lower extremities and pelvic veins, caused by aplasia of the inferior vena cava. After thrombotic complications caused by vena cava aplasia there is high risk of recurrence. Those patients should be anticoagulated for lifetime.


VASA ◽  
2014 ◽  
Vol 43 (1) ◽  
pp. 73-77 ◽  
Author(s):  
Paweł Gać ◽  
Małgorzata Kuśmierska ◽  
Przemysław Jaźwiec ◽  
Magdalena Bolt ◽  
Anna Kuśmierska ◽  
...  

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