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Living related partial liver transplantation for hyperammonemia due to congenital absence of the portal vein

โœ Scribed by M Shinkai; Y Ohhama; T Nishi; H Yamamoto; S Fujita; H Take; M Adachi; K Tachibana; N Aida; K Kato; Y Tanaka; S Takemiya; K Tanaka


Book ID
117229697
Publisher
Elsevier Science
Year
2000
Tongue
English
Weight
59 KB
Volume
32
Category
Article
ISSN
0041-1345

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Congenital absence of the portal vein (CAPV) with an extrahepatic portosystemic shunt is a rare malformation; the completely absent type, Abernethy malformation type I, is especially rare. Liver transplantation for CAPV type I has been recently recognized as the only curative operation, but few repo

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## Congenital absence of the portal vein (CAPV) is a very rare venous malformation in which mesenteric venous blood drains directly into the systemic circulation. There is no portal perfusion of the liver and no portal hypertension. This abnormality is usually coincidentally discovered in children,