Spleen

The spleen is an organ found in virtually all vertebrates. Similar in structure to a large lymph node, it acts primarily as a blood filter. The word spleen comes from Ancient Greek σπλήν (splḗn).[1]

For other uses, see Spleen (disambiguation).
This article uses anatomical terminology.
Spleen
The human spleen is located in the upper left abdomen, behind the stomach
Details
SystemImmune system (Lymphatic system)
ArterySplenic artery
VeinSplenic vein
NerveSplenic plexus
Identifiers
Latinsplen, lien
MeSHD013154
TAA13.2.01.001
FMA7196
Anatomical terminology
A 3D medical animation still of spleen structure & exact location

The spleen plays important roles in regard to red blood cells (erythrocytes) and the immune system.[2] It removes old red blood cells and holds a reserve of blood, which can be valuable in case of hemorrhagic shock, and also recycles iron. As a part of the mononuclear phagocyte system, it metabolizes hemoglobin removed from senescent red blood cells (erythrocytes). The globin portion of hemoglobin is degraded to its constitutive amino acids, and the heme portion is metabolized to bilirubin, which is removed in the liver.[3]

The spleen synthesizes antibodies in its white pulp and removes antibody-coated bacteria and antibody-coated blood cells by way of blood and lymph node circulation. These monocytes, upon moving to injured tissue (such as the heart after myocardial infarction), turn into dendritic cells and macrophages while promoting tissue healing.[4][5][6] The spleen is a center of activity of the mononuclear phagocyte system and is analogous to a large lymph node, as its absence causes a predisposition to certain infections.[7]

In humans the spleen is purple in color and is in the left upper quadrant of the abdomen.[3][8]

Anatomy

The spleen is underneath the left part of the diaphragm, and has a smooth, convex surface that faces the diaphragm. It is underneath the ninth, tenth, and eleventh ribs. The other side of the spleen is divided by a ridge into two regions: an anterior gastric portion, and a posterior renal portion. The gastric surface is directed forward, upward, and toward the middle, is broad and concave, and is in contact with the posterior wall of the stomach. Below this it is in contact with the tail of the pancreas. The renal surface is directed medialward and downward. It is somewhat flattened, considerably narrower than the gastric surface, and is in relation with the upper part of the anterior surface of the left kidney and occasionally with the left adrenal gland.

Measurements
90% confidence interval of maximum spleen length by abdominal ultrasonography by height of the person[9]
HeightSpleen length
WomenMen
155–159 cm6.4–12 cm
160–164 cm7.4–12.2 cm8.9–11.3 cm
165–169 cm7.5–11.9 cm8.5–12.5 cm
170–174 cm8.3–13.0 cm8.6–13.1 cm
175–179 cm8.1–12.3 cm8.6–13.4 cm
180–184 cm9.3–13.4 cm
185–189 cm9.3–13.6 cm
190–194 cm9.7–14.3 cm
195–199 cm10.2–14.4 cm

The spleen, in healthy adult humans, is approximately 7 centimetres (2.8 in) to 14 centimetres (5.5 in) in length.

An easy way to remember the anatomy of the spleen is the 1×3×5×7×9×10×11 rule. The spleen is 1 by 3 by 5 inches (3 by 8 by 13 cm), weighs approximately 7 oz (200 g), and lies between the 9th and 11th ribs on the left-hand side and along the axis of 10th rib. The weight varies between 1 oz (28 g) and 8 oz (230 g) (standard reference range),[10] correlating mainly to height, body weight and degree of acute congestion but not to sex or age.[11]

  • Spleen seen on abdominal ultrasonography
  • Maximum length of spleen on abdominal ultrasonography
  • Back of lumbar region, showing surface markings for kidneys, ureters, and spleen
  • Side of thorax, showing surface markings for bones, lungs (purple), pleura (blue), and spleen (green)

Blood supply
Visceral surface of the spleen

Near the middle of the spleen is a long fissure, the hilum, which is the point of attachment for the gastrosplenic ligament and the point of insertion for the splenic artery and splenic vein. There are other openings present for lymphatic vessels and nerves.

Like the thymus, the spleen possesses only efferent lymphatic vessels. The spleen is part of the lymphatic system. Both the short gastric arteries and the splenic artery supply it with blood.[12]

The germinal centers are supplied by arterioles called penicilliary radicles.[13]

Nerve supply

The spleen is innervated by the splenic plexus, which connects a branch of the celiac ganglia to the vagus nerve.

The underlying central nervous processes coordinating the spleen's function seem to be embedded into the Hypothalamic-pituitary-adrenal-axis, and the brainstem, especially the subfornical organ.[14]

Development

The spleen is unique in respect to its development within the gut. While most of the gut organs are endodermally derived (with the exception of the neural-crest derived adrenal gland), the spleen is derived from mesenchymal tissue.[15] Specifically, the spleen forms within, and from, the dorsal mesentery. However, it still shares the same blood supply—the celiac trunk—as the foregut organs.

Function

Pulp
Micrograph of splenic tissue showing the red pulp (red), white pulp (blue) and a thickened inflamed capusule (mostly pink – top of image). H&E stain.
The spleen contains two different tissues, white pulp (A) and red pulp (B). The white pulp functions in producing and growing immune and blood cells. The red pulp functions in filtering blood of antigens, microorganisms, and defective or worn-out red blood cells.
AreaFunctionComposition
red pulpMechanical filtration of red blood cells. In mice: Reserve of monocytes[4]
white pulpActive immune response through humoral and cell-mediated pathways.Composed of nodules, called Malpighian corpuscles. These are composed of:

Other

Other functions of the spleen are less prominent, especially in the healthy adult:

  • Spleen produces all types of blood cells during fetal life
  • Production of opsonins, properdin, and tuftsin.
  • Creation of red blood cells. While the bone marrow is the primary site of hematopoiesis in the adult, the spleen has important hematopoietic functions up until the fifth month of gestation. After birth, erythropoietic functions cease, except in some hematologic disorders. As a major lymphoid organ and a central player in the reticuloendothelial system, the spleen retains the ability to produce lymphocytes and, as such, remains a hematopoietic organ.
  • Storage of red blood cells, lymphocytes and other formed elements. The spleen of horses stores roughly 30% of the red blood cells and can release them when needed.[16] In humans, up to a cup (240 ml) of red blood cells is held in the spleen and released in cases of hypovolemia[17] and hypoxia.[18] It can store platelets in case of an emergency and also clears old platelets from the circulation. Up to a quarter of lymphocytes are stored in the spleen at any one time.

Clinical significance
Thalassemia enlarged spleen after splenectomy

Enlarged spleen
Main article: Splenomegaly

Enlargement of the spleen is known as splenomegaly. It may be caused by sickle cell anemia, sarcoidosis, malaria, bacterial endocarditis, leukemia, pernicious anemia, Gaucher's disease, leishmaniasis, Hodgkin's disease, Banti's disease, hereditary spherocytosis, cysts, glandular fever (mononucleosis or 'Mono' caused by the Epstein–Barr virus), and tumours. Primary tumors of the spleen include hemangiomas and hemangiosarcomas. Marked splenomegaly may result in the spleen occupying a large portion of the left side of the abdomen.

The spleen is the largest collection of lymphoid tissue in the body. It is normally palpable in preterm infants, in 30% of normal, full-term neonates, and in 5% to 10% of infants and toddlers. A spleen easily palpable below the costal margin in any child over the age of 3–4 years should be considered abnormal until proven otherwise.

Splenomegaly can result from antigenic stimulation (e.g., infection), obstruction of blood flow (e.g., portal vein obstruction), underlying functional abnormality (e.g., hemolytic anemia), or infiltration (e.g., leukemia or storage disease, such as Gaucher's disease). The most common cause of acute splenomegaly in children is viral infection, which is transient and usually moderate. Basic work-up for acute splenomegaly includes a complete blood count with differential, platelet count, and reticulocyte and atypical lymphocyte counts to exclude hemolytic anemia and leukemia. Assessment of IgM antibodies to viral capsid antigen (a rising titer) is indicated to confirm Epstein–Barr virus or cytomegalovirus. Other infections should be excluded if these tests are negative.

Rupture of spleen

Traumas, such as a road traffic collision, can cause rupture of the spleen, which is a situation requiring immediate medical attention.

Asplenia
Main article: Asplenia

Asplenia refers to a non-functioning spleen, which may be congenital, or caused by traumatic injury, surgical resection (splenectomy) or a disease such as sickle cell anaemia. Hyposplenia refers to a partially functioning spleen. These conditions may cause[5] a modest increase in circulating white blood cells and platelets, a diminished response to some vaccines, and an increased susceptibility to infection. In particular, there is an increased risk of sepsis from polysaccharide encapsulated bacteria. Encapsulated bacteria inhibit binding of complement or prevent complement assembled on the capsule from interacting with macrophage receptors. Phagocytosis needs natural antibodies, which are immunoglobulins that facilitate phagocytosis either directly or by complement deposition on the capsule. They are produced by IgM memory B cells (a subtype of B cells) in the marginal zone of the spleen.[19][20]

A splenectomy (removal of the spleen) results in a greatly diminished frequency of memory B cells.[21] A 28-year follow-up of 740 World War II veterans whose spleens were removed on the battlefield showed a significant increase in the usual death rate from pneumonia (6 rather than the expected 1.3) and an increase in the death rate from ischemic heart disease (41 rather than the expected 30), but not from other conditions.[22]

Accessory spleen

An accessory spleen is a small splenic nodule extra to the spleen usually formed in early embryogenesis. Accessory spleens are found in approximately 10 percent of the population[23] and are typically around 1 centimeter in diameter. Splenosis is a condition where displaced pieces of splenic tissue (often following trauma or splenectomy) autotransplant in the abdominal cavity as accessory spleens.[24]

Polysplenia is a congenital disease manifested by multiple small accessory spleens,[25] rather than a single, full-sized, normal spleen. Polysplenia sometimes occurs alone, but it is often accompanied by other developmental abnormalities such as intestinal malrotation or biliary atresia, or cardiac abnormalities, such as dextrocardia. These accessory spleens are non-functional.

Infarction
Main article: Splenic infarction

Splenic infarction is a condition in which blood flow supply to the spleen is compromised[26], leading to partial or complete infarction (tissue death due to oxygen shortage) in the organ.[27]

Splenic infarction occurs when the splenic artery or one of its branches are occluded, for example by a blood clot. Although it can occur asymptomatically, the typical symptom is severe pain in the left upper quadrant of the abdomen, sometimes radiating to the left shoulder. Fever and chills develop in some cases.[28] It has to be differentiated from other causes of acute abdomen.

Hyaloserositis

The spleen may be affected by hyaloserositis, in which it is coated with fibrous hyaline.[29][30]

Society and culture

The word spleen comes from the Ancient Greek σπλήν (splḗn), and is the idiomatic equivalent of the heart in English, i.e., to be good-spleened (εὔσπλαγχνος, eúsplankhnos) means to be good-hearted or compassionate.[31]

In English the word spleen was customary during the period of the 18th century. Authors like Richard Blackmore or George Cheyne employed it to characterise the hypochondriacal and hysterical affections.[32][33] William Shakespeare, in Julius Caesar uses the spleen to describe Cassius's irritable nature.

Must I observe you? must I stand and crouch
Under your testy humour? By the gods
You shall digest the venom of your spleen,
Though it do split you; for, from this day forth,
I'll use you for my mirth, yea, for my laughter,
When you are waspish.[34]

In French, "splénétique" refers to a state of pensive sadness or melancholy. It has been popularized by the poet Charles Baudelaire (1821–1867) but was already used before in particular to the Romantic literature (19th century). The French word for the organ is "rate".

The connection between spleen (the organ) and melancholy (the temperament) comes from the humoral medicine of the ancient Greeks. One of the humours (body fluid) was the black bile, secreted by the spleen organ and associated with melancholy. In eighteenth- and nineteenth-century England, women in bad humor were said to be afflicted by the spleen, or the vapours of the spleen. In modern English, "to vent one's spleen" means to vent one's anger, e.g., by shouting, and can apply to both males and females. Similarly, the English term "splenetic" describes a person in a foul mood.

In contrast, the Talmud (tractate Berachoth 61b) refers to the spleen as the organ of laughter while possibly suggesting a link with the humoral view of the organ. Sanhedrin 21b and Avodah Zarah 44a (and Rashi ibid.) additionally describe how in the ancient world, some runners destroyed their spleens with drugs to increase their speed, and hollowed out the soles of their feet of flesh so as not to feel thorns and thistles as they ran.

The spleen also plays an important role in traditional Chinese medicine and is the Yin part of the Earth element paired with its Yang counterpart the Stomach.

Other animals
Laparoscopic view of a horse's spleen (the purple and grey mottled organ)

In cartilaginous and ray-finned fish, it consists primarily of red pulp and is normally somewhat elongated, as it lies inside the serosal lining of the intestine. In many amphibians, especially frogs, it has the more rounded form and there is often a greater quantity of white pulp.[35]. A study published in 2009 using mice found that the red pulp of the spleen forms a reservoir that contains over half of the body's monocytes.[4]

In reptiles, birds, and mammals, white pulp is always relatively plentiful, and in birds and mammals the spleen is typically rounded, but it adjusts its shape somewhat to the arrangement of the surrounding organs. In most vertebrates, the spleen continues to produce red blood cells throughout life; only in mammals this function is lost in middle-aged adults. Many mammals have tiny spleen-like structures known as haemal nodes throughout the body that are presumed to have the same function as the spleen.[35] The spleens of aquatic mammals differ in some ways from those of fully land-dwelling mammals; in general they are bluish in colour. In cetaceans and manatees they tend to be quite small, but in deep diving pinnipeds, they can be massive, due to their function of storing red blood cells.

The only vertebrates lacking a spleen are the lampreys and hagfishes (the Cyclostomata). Even in these animals, there is a diffuse layer of haematopoeitic tissue within the gut wall, which has a similar structure to red pulp and is presumed homologous with the spleen of higher vertebrates.[35]

In mice the spleen stores half the body's monocytes so that upon injury, they can migrate to the injured tissue and transform into dendritic cells and macrophages to assist wound healing.[4]

Additional images
  • Transverse section of the spleen, showing the trabecular tissue and the splenic vein and its tributaries
  • Spleen
  • Laparoscopic view of human spleen
gollark: =tex 1 - (1 - \frac{P_{covid}}{P})^{N_{gathering}}
gollark: Couldn't this just be done as `1 - ((1 - positives/population) ^ gathering)`?
gollark: Christ is his own antiparticle, so originally just Christ, not sure about the remaining one.
gollark: I would be impressed if they managed to get tracking beacons with reasonable range and battery life to actually fit.
gollark: Yes, it's not really a *significant* issue compared to the bigger ones of spreading disease, but it is there.

See also

References
  1. σπλήν, Henry George Liddell, Robert Scott, A Greek-English Lexicon, on Perseus Digital Library
  2. Darling, David. "spleen". www.daviddarling.info.
  3. Mebius, RE; Kraal, G (2005). "Structure and function of the spleen". Nature Reviews. Immunology. 5 (8): 606–16. doi:10.1038/nri1669. PMID 16056254.
  4. Swirski, FK; Nahrendorf, M; Etzrodt, M; Wildgruber, M; Cortez-Retamozo, V; Panizzi, P; Figueiredo, JL; Kohler, RH; Chudnovskiy, A; Waterman, P; Aikawa, E; Mempel, TR; Libby, P; Weissleder, R; Pittet, MJ (2009). "Identification of splenic reservoir monocytes and their deployment to inflammatory sites". Science. 325 (5940): 612–16. Bibcode:2009Sci...325..612S. doi:10.1126/science.1175202. PMC 2803111. PMID 19644120.
  5. Jia, T; Pamer, EG (2009). "Immunology. Dispensable but not irrelevant". Science. 325 (5940): 549–50. Bibcode:2009Sci...325..549J. doi:10.1126/science.1178329. PMC 2917045. PMID 19644100.
  6. "Finally, the Spleen Gets Some Respect" By Natalie Angier, The New York Times, August 3, 2009
  7. Brender, Erin (2005-11-23). Richard M. Glass (ed.). Illustrated by Allison Burke. "Spleen Patient Page". Journal of the American Medical Association. 294 (20): 2660. doi:10.1001/jama.294.20.2660. PMID 16304080.
  8. Loscalzo, Joseph; Fauci, Anthony S.; Braunwald, Eugene; Dennis L. Kasper; Hauser, Stephen L; Longo, Dan L. (2008). Harrison's principles of internal medicine. McGraw-Hill Medical. ISBN 978-0-07-146633-2.
  9. Chow, Kai Uwe; Luxembourg, Beate; Seifried, Erhard; Bonig, Halvard (2016). "Spleen Size Is Significantly Influenced by Body Height and Sex: Establishment of Normal Values for Spleen Size at US with a Cohort of 1200 Healthy Individuals". Radiology. 279 (1): 306–13. doi:10.1148/radiol.2015150887. ISSN 0033-8419. PMID 26509293.
  10. Molina, D. Kimberley; DiMaio, Vincent J.M. (2012). "Normal Organ Weights in Men". The American Journal of Forensic Medicine and Pathology. 33 (4): 368–372. doi:10.1097/PAF.0b013e31823d29ad. ISSN 0195-7910. PMID 22182984.
  11. Sprogøe-Jakobsen, Susan; Sprogøe-Jakobsen, Ulrik (1997). "The weight of the normal spleen". Forensic Science International. 88 (3): 215–223. doi:10.1016/S0379-0738(97)00103-5. ISSN 0379-0738. PMID 9291593.
  12. Blackbourne, Lorne H (2008). Surgical recall. Lippincott Williams & Wilkins. p. 259. ISBN 978-0-7817-7076-7.
  13. "Penicilliary radicles". Medical-dictionary.thefreedictionary.com. Retrieved 2011-04-03.
  14. Lori, Andrea; Perrotta, Marialuisa; Lembo, Giuseppe; Carnevale, Daniela (2017-06-07). "The Spleen: A Hub Connecting Nervous and Immune Systems in Cardiovascular and Metabolic Diseases". International Journal of Molecular Sciences. 18 (6): 1216. doi:10.3390/ijms18061216. ISSN 1422-0067. PMC 5486039. PMID 28590409.
  15. Vellguth, Swantje; Brita von Gaudecker; Hans-Konrad Müller-Hermelink (1985). "The development of the human spleen". Cell and Tissue Research. 242 (3): 579–92. doi:10.1007/BF00225424. PMID 4075378.
  16. Carey, Bjorn (May 5, 2006). "Horse science: What makes a Derby winner – Spleen acts as a 'natural blood doper,' scientist says". NBC News. Retrieved 2006-05-09.
  17. "Spleen: Information, Surgery and Functions". Chp.edu. Childrens Hospital of Pittsburgh. 2010-11-17. Archived from the original on 2011-09-26. Retrieved 2011-04-03.
  18. Lodin-Sundström, Angelica; Schagatay, Erika (June 2010). "Spleen contraction during 20 min normobaric hypoxia and 2 min apnea in humans". Aviation, Space, and Environmental Medicine. 8 (6): 545–49. doi:10.3357/ASEM.2682.2010. PMID 20540444.
  19. Di Sabatino, A; Carsetti, R; Corazza, GR (Jul 2, 2011). "Post-splenectomy and hyposplenic states". Lancet. 378 (9785): 86–97. doi:10.1016/S0140-6736(10)61493-6. PMID 21474172.
  20. Carsetti, R; Rosado, MM; Wardmann, H (February 2004). "Peripheral development of B cells in mouse and man". Immunological Reviews. 197: 179–91. doi:10.1111/j.0105-2896.2004.0109.x. PMID 14962195.
  21. Kruetzmann, S; Rosado, MM; Weber, H; Germing, U; Tournilhac, O; Peter, HH; Berner, R; Peters, A; Boehm, T; Plebani, A; Quinti, I; Carsetti, R (Apr 7, 2003). "Human immunoglobulin M memory B cells controlling Streptococcus pneumoniae infections are generated in the spleen". The Journal of Experimental Medicine. 197 (7): 939–45. doi:10.1084/jem.20022020. PMC 2193885. PMID 12682112.
  22. Dennis Robinette, C.; Fraumeni, Josephf. (1977). "Splenectomy and Subsequent Mortality in Veterans of the 1939–45 War". The Lancet. 310 (8029): 127–29. doi:10.1016/S0140-6736(77)90132-5. PMID 69206.
  23. Moore, Keith L. (1992). Clinically Oriented Anatomy (3rd ed.). Baltimore: Williams & Wilkins. p. 187. ISBN 978-0-683-06133-8.
  24. Abu Hilal M; Harb A; Zeidan B; Steadman B; Primrose JN; Pearce NW (January 5, 2009). "Hepatic splenosis mimicking HCC in a patient with hepatitis C liver cirrhosis and mildly raised alpha feto protein; the important role of explorative laparoscopy". World Journal of Surgical Oncology. 7 (1): 1. doi:10.1186/1477-7819-7-1. PMC 2630926. PMID 19123935.
  25. "polysplenia" at Dorland's Medical Dictionary
  26. Chapman, J; Bhimji, SS (2018), "article-29380", Splenic Infarcts, Treasure Island (FL): StatPearls Publishing, PMID 28613652, retrieved 2019-02-27
  27. Jaroch MT, Broughan TA, Hermann RE (October 1986). "The natural history of splenic infarction". Surgery. 100 (4): 743–50. PMID 3764696.
  28. Nores, M1; Phillips, EH; Morgenstern, L; Hiatt, JR (February 1998). "The Clinical Spectrum of Splenic Infarction". The American Surgeon. 64 (2): 182–88. PMID 9486895.
  29. "Hyaloserositis". Online Medical Dictionary. Accessed on: June 21, 2008.
  30. "Sugar-coated spleen". Drugs.com.
  31. Robertson's Word Pictures of the New Testament, commentary on 1 Peter 3:8
  32. Cheyne, George: The English Malady; or, A Treatise of Nervous Diseases of All Kinds, as Spleen, Vapours, Lowness of Spirits, Hypochondriacal and Hysterical Distempers with the Author's Own Case at Large, Dublin, 1733. Facsimile ed., ed. Eric T. Carlson, M.D., 1976, Scholars' Facsimiles & Reprints, ISBN 978-0-8201-1281-7
  33. Blackmore, Richard: Treatise of the spleen and vapors. London, 1725
  34. Julius Caesar by William Shakespeare Act 4:1
  35. Romer, Alfred Sherwood; Parsons,, Thomas S. (1977). The Vertebrate Body. Philadelphia: Holt-Saunders International. pp. 410–11. ISBN 978-0-03-910284-5.CS1 maint: multiple names: authors list (link)
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.