Congenital absence of the portal vein (CAPV) is a rare malformation of the mesenteric vasculature in which visceral venous blood bypasses the liver, completely draining into the systemic circulation through a congenital porto-systemic shunt. Liver transplantation has rarely been indicated for patien
Living related partial liver transplantation for hyperammonemia due to congenital absence of the portal vein
โ 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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๐ SIMILAR VOLUMES
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
## 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,