Lobules of liver

(Redirected from Bridging fibrosis)

In histology (microscopic anatomy), the lobules of liver, or hepatic lobules, are small divisions of the liver defined at the microscopic scale. The hepatic lobule is a building block of the liver tissue, consisting of a portal triad, hepatocytes arranged in linear cords between a capillary network, and a central vein.

Lobules of liver
The structure of the liver’s functional units or lobules. Blood enters the lobules through branches of the portal vein and hepatic artery proper, then flows through sinusoids.
Details
SystemDigestive system
LocationLiver
Identifiers
Latinlobuli hepatis
TA98A05.8.01.056
TA23060
FMA76488
Anatomical terms of microanatomy

Lobules are different from the lobes of liver: they are the smaller divisions of the lobes. The two-dimensional microarchitecture of the liver can be viewed from different perspectives:[1]

Name Shape Model
classical lobule[2] hexagonal; divided into concentric centrilobular, midzonal, periportal parts anatomical
portal lobule[3] triangular; centered on a portal triad bile secretion
acinus [4] elliptical or diamond-shaped; divided into zone I (periportal), zone II (transition zone), and zone III (pericentral) blood flow and metabolic

The term "hepatic lobule", without qualification, typically refers to the classical lobule.

Structure

edit

The hepatic lobule can be described in terms of metabolic "zones", describing the hepatic acinus (terminal acinus). Each zone is centered on the line connecting two portal triads and extends outwards to the two adjacent central veins. The periportal zone I is nearest to the entering vascular supply and receives the most oxygenated blood, making it least sensitive to ischemic injury while making it very susceptible to viral hepatitis. Conversely, the centrilobular zone III has the poorest oxygenation, and will be most affected during a time of ischemia.[5]

Portal triad

edit

A portal triad (also known as portal canal, portal field[citation needed], portal area[citation needed], or portal tract[citation needed]) is a distinctive arrangement within lobules. It consists of the following five structures:[6]

The misnomer "portal triad" traditionally has included only the first three structures, and was named before lymphatic vessels were discovered in the structure.[7][8] It can refer both to the largest branch of each of these vessels running inside the hepatoduodenal ligament, and to the smaller branches of these vessels inside the liver.

In the smaller portal triads, the four vessels lie in a network of connective tissue and are surrounded on all sides by hepatocytes. The ring of hepatocytes abutting the connective tissue of the triad is called the periportal limiting plate.

Periportal space

edit

The periportal space (Latin: spatium periportale), or periportal space of Mall,[9] is a space between the stroma of the portal canal and the outermost hepatocytes in the hepatic lobule, and is thought to be one of the sites where lymph originates in the liver.[10]

Fluid (residual blood plasma) that is not taken up by hepatocytes drains into the periportal space, and is taken up by the lymphatic vessels that accompany the other portal triad constituents.

Function

edit
 
Oxygenation zones are numbered inside the diamond-shaped acinus (in red). Zone three is closest to the central vein and zone one is closest to the portal triad

Zones differ by function:

Other zonal injury patterns include zone I deposition of hemosiderin in hemochromatosis and zone II necrosis in yellow fever.[11]

Clinical significance

edit

Bridging fibrosis, a type of fibrosis seen in several types of liver injury, describes fibrosis from the central vein to the portal triad.[13]

See also

edit

References

edit
  1. ^ Cell and Tissue Structure at U. Va.
  2. ^ Histology image: 88_03 at the University of Oklahoma Health Sciences Center
  3. ^ Histology image: 88_09a at the University of Oklahoma Health Sciences Center
  4. ^ Histology image: 88_09b at the University of Oklahoma Health Sciences Center
  5. ^ B.R. Bacon; J.G. O'Grady; A.M. Di Bisceglie; J.R. Lake (2006). Comprehensive Clinical Hepatology. Elsevier Health Sciences. ISBN 0-323-03675-9.
  6. ^ Mescher, Anthony L. (2013). Junqueira's Basic Histology text and atlas. McGraw-Hill Education. p. 333. ISBN 978-0-07-180720-3.
  7. ^ Vander's Human Physiology, The Mechanisms of Body Function. 26 September 2016. ISBN 9781478436232.
  8. ^ "Physiology of the Hepatic Vascular System". www.vivo.colostate.edu. Retrieved 2018-12-04.
  9. ^ Roderick N. M. MacSween (2007). MacSween's pathology of the liver. Elsevier Health Sciences. pp. 44–. ISBN 978-0-443-10012-3. Retrieved 23 May 2011.
  10. ^ Ross, Michael H.; Pawlina, Wojciech (2006). Histology: A Text and Atlas. Lippincott Williams & Wilkins. p. 426. ISBN 0-7817-7221-4.
  11. ^ a b E.R. Schiff; M.F. Sorrell; W.C. Maddrey, eds. (2007). Schiff's Diseases of the Liver, Tenth Edition. Lippincott William & Wilkins. ISBN 978-0-7817-6040-9.
  12. ^ M.J. Burns; S.L. Friedman; A.M. Larson (2009). "Acetaminophen (paracetamol) poisoning in adults: Pathophysiology, presentation, and diagnosis". In D.S. Basow (ed.). UpToDate. Waltham, MA: UpToDate.
  13. ^ "The liver ~ Medical student education – Tissupath". tissupath.com.au. Retrieved 20 June 2018.
edit