Abernethy malformation

Abernethy malformations are rare vascular anomalies of the splanchnic venous system. They consist of congenital portosystemic shunts and result from persistence of the embryonic vessels.

Epidemiology

Type I malformations are thought to occur only in females, while type II have a male predominance .

Pathology

Subtypes

There are two main types of Abernethy malformations that have been described (initially devised by G Morgan and R Superina ):

• type I: end-to-side shunt; superior mesenteric and splenic vein drain separately into inferior vena cava
• type II: side-to-side shunts; superior mesenteric vein and splenic vein form a common trunk before draining into the inferior vena cava

In type I shunts (end-to-end), there is a congenital absence of the portal vein with a complete diversion of portal blood into systemic veins (inferior vena cava, renal veins, or iliac veins). These are further subdivided into:

• type Ia: separate drainage of the superior mesenteric vein and splenic vein into systemic veins
• type Ib: superior mesenteric vein and splenic vein join to form a short extra-hepatic portal vein which drains into a systemic vein (inferior vena cava, right atrium or iliac veins)

In type II shunts (side-to-side), there is a hypoplastic portal vein with portal blood diversion into the inferior vena cava through a side-to-side, extrahepatic communication.

Associations

• hepatic encephalopathy: from portosystemic shunting
• hepatic mass lesions 
  • focal nodular hyperplasia: thought to generate due to the absence of the portal vein
  • hepatocellular carcinoma
  • hepatoblastoma
• hepatopulmonary syndrome 
• pulmonary arteriovenous fistulae
  • thought to arise due to hyperammonemia
  • may lead to systemic emboli
• other congenital abnormalities, particularly associated with type I :
  • congenital cardiac anomalies
  • biliary atresia
  • polysplenia

History and etymology

Named after John Abernethy, who gave the first account of an absent portal vein with accompanying congenital mesentericocaval shunt in 1793.

Siehe auch:

• portosystemische Umgehungskreisläufe
• Herzfehler
• hepatozelluläres Karzinom
• Hepatoblastom
• Fokale noduläre Hyperplasie
• Hepatische Enzephalopathie
• angeborener intrahepatischer portosystemischer Shunt
• Hepatopulmonales Syndrom
• Polysplenie-Syndrom
• Gallengangatresie

und weiter:

• Pfortaderthrombose
• absence of intraheptic portal vein