Portal vein

This article is about the vein connected to the liver. For veins connecting two systems of capillary beds, see portal venous system.
portal vein

The portal vein and its tributaries. It is formed by the superior mesenteric vein, inferior mesenteric vein, and splenic vein. Lienal vein is an old term for splenic vein.
Details
Drains from Gastrointestinal tract, spleen, pancreas
Source
 splenic vein, superior mesenteric vein, inferior mesenteric vein
Drains to liver sinusoid
Identifiers
Latin vena portae hepatis
MeSH A07.231.908.670.567
TA A12.3.12.001
FMA 50735

Anatomical terminology

The portal vein or hepatic portal vein is a blood vessel that carries blood from the gastrointestinal tract and spleen to the liver. This blood is rich in nutrients that have been extracted from food, and the liver processes these nutrients; it also filters toxins that may have been ingested with the food. 75% of total liver blood flow is through the portal vein, with the remainder coming from the hepatic artery proper. The blood leaves the liver to the heart in the hepatic veins.

The portal vein is not a true vein, because it conducts blood to capillary beds in the liver and not directly to the heart. It is a major component of the hepatic portal system, one of only two portal venous systems in the body – with the hypophyseal portal system being the other.

The portal vein is usually formed by the confluence of the superior mesenteric and splenic veins and also receives blood from the inferior mesenteric, gastric, and cystic veins.

Conditions involving the portal vein cause considerable illness and death. An important example of such a condition is elevated blood pressure in the portal vein. This condition, called portal hypertension, is a major complication of cirrhosis.

Structure

Tributaries of the hepatic portal vein[1]

Measuring approximately 8 cm (3 inches) in adults,[2] the portal vein is located in the right upper quadrant of the abdomen, originating behind the neck of the pancreas.[3]

In most individuals, the portal vein is formed by the union of the superior mesenteric vein and the splenic vein.[4] For this reason, the portal vein is occasionally called the splenic-mesenteric confluence.[3] Occasionally, the portal vein also directly communicates with the inferior mesenteric vein, although this is highly variable. Other tributaries of the portal vein include the cystic and gastric veins.[1]

Immediately before reaching the liver, the portal vein divides into right and left. It ramifies further, forming smaller venous branches and ultimately portal venules. Each portal venule courses alongside a hepatic arteriole and the two vessels form the vascular components of the portal triad. These vessels ultimately empty into the hepatic sinusoids to supply blood to the liver.[1]

Portacaval anastomoses

The portal venous system has several anastomoses with the systemic venous system. In cases of portal hypertension these anastamoses may become engorged, dilated, or varicosed and subsequently rupture.

Accessory hepatic portal veins

Accessory hepatic portal veins are those veins that drain directly into the liver without joining the hepatic portal vein. These include the paraumbilical veins as well as veins of the lesser omentum, falciform ligament, and those draining the gallbladder wall.[3]

Function

The portal vein and hepatic arteries form the liver's dual blood supply. Approximately 75% of hepatic blood flow is derived from the portal vein, while the remainder is from the hepatic arteries.[3]

Unlike most veins, the portal vein does not drain into the heart. Rather, it is part of a portal venous system that delivers venous blood into another capillary system, the hepatic sinusoids of the liver. In carrying venous blood from the gastrointestinal tract to the liver, the portal vein accomplishes two tasks: it supplies the liver with metabolic substrates and it ensures that substances ingested are first processed by the liver before reaching the systemic circulation. This accomplishes two things. First, possible toxins that may be ingested can be detoxified by the hepatocytes before they are released into the systemic circulation. Second, the liver is the first organ to absorb nutrients just taken in by the intestines. After draining into the liver sinusoids, blood from the liver is drained by the hepatic vein.

Clinical significance

Portal hypertension

Main article: Portal hypertension

Increased blood pressure in the portal vein, called portal hypertension, is a major complication of liver disease, most commonly cirrhosis.[5] Signs of portal hypertension include those of chronic liver disease: ascites, esophageal varices, spider nevi, caput medusae, and palmar erythema.[6]

Pylephlebitis

Main article: Pylephlebitis

Pylephlebitis is infection of the portal vein, usually arising from an infectious intraabdominal process such as diverticulosis.[7][8]

References

  1. 1 2 3 Henry Gray (1901). Anatomy, Descriptive and Surgical (16 ed.). Philadelphia: Lea Brothers. p. 619.
  2. ↑ Harold M Chung; Chung, Kyung Won (2008). Gross anatomy. Philadelphia: Wolters Kluwer Health/Lippincott Williams & Wilkins. p. 208. ISBN 0-7817-7174-9.
  3. 1 2 3 4 Plinio Rossi; L. Broglia (2000). Portal Hypertension: Diagnostic Imaging and Imaging-Guided Therapy. Berlin: Springer. p. 51. ISBN 3-540-65797-5.
  4. ↑ Benjamin L. Shneider; Sherman, Philip M. (2008). Pediatric Gastrointestinal Disease. Connecticut: PMPH-USA. p. 751. ISBN 1-55009-364-9.
  5. ↑ Dooley, James; Sherlock, Sheila (2002). Diseases of the liver and biliary system. Oxford: Blackwell Science. ISBN 0-632-05582-0.
  6. ↑ Key Topics in General Surgery (2 ed.). Informa Healthcare. 2002. ISBN 1-85996-164-9.
  7. ↑ Plemmons RM, Dooley DP, Longfield RN (November 1995). "Septic thrombophlebitis of the portal vein (pylephlebitis): diagnosis and management in the modern era". Clin. Infect. Dis. 21 (5): 1114–20. doi:10.1093/clinids/21.5.1114. PMID 8589130.
  8. ↑ Perez-Cruet MJ, Grable E, Drapkin MS, Jablons DM, Cano G (May 1993). "Pylephlebitis associated with diverticulitis". South. Med. J. 86 (5): 578–80. doi:10.1097/00007611-199305000-00020. PMID 8488411.

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External links

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