Parathyroid gland

Parathyroid glands
Diagram showing structures in the human neck. The four green shaded areas represent the most common position of the parathyroid glands, which are generally four in number and situated behind the lateral lobes of the thyroid gland (shaded orange).
Thyroid and parathyroids as viewed from the front of the neck
Details
PrecursorNeural crest mesenchyme and third and fourth pharyngeal pouch endoderm
SystemEndocrine
ArterySuperior thyroid artery, inferior thyroid artery,
VeinSuperior thyroid vein, middle thyroid vein, inferior thyroid vein,
NerveMiddle cervical ganglion, inferior cervical ganglion
LymphPretracheal, prelaryngeal, jugulodigastric lymph nodes
Identifiers
Latinglandula parathyreoidea inferior, glandula parathyreoidea superior
MeSHD010280
TA98A11.4.00.001
TA23870
FMA13890
Anatomical terminology

Parathyroid glands are small endocrine glands in the neck of humans and other tetrapods. Humans usually have four parathyroid glands, located on the back of the thyroid gland in variable locations. The parathyroid gland produces and secretes parathyroid hormone in response to low blood calcium, which plays a key role in regulating the amount of calcium in the blood and within the bones.

Parathyroid glands share a similar blood supply, venous drainage, and lymphatic drainage to the thyroid glands. Parathyroid glands are derived from the epithelial lining of the third and fourth pharyngeal pouches, with the superior glands arising from the fourth pouch and the inferior glands arising from the higher third pouch. The relative position of the inferior and superior glands, which are named according to their final location, changes because of the migration of embryological tissues.

Hyperparathyroidism and hypoparathyroidism, characterized by alterations in the blood calcium levels and bone metabolism, are states of either surplus or deficient parathyroid function.

Structure

The parathyroid glands are two pairs of glands usually positioned behind the left and right lobes of the thyroid. Each gland is a yellowish-brown flat ovoid that resembles a lentil seed, usually about 6 mm long and 3 to 4 mm wide, and 1 to 2 mm anteroposteriorly.[1] There are typically four parathyroid glands. The two parathyroid glands on each side which are positioned higher are called the superior parathyroid glands, while the lower two are called the inferior parathyroid glands. Healthy parathyroid glands generally weigh about 30 mg in men and 35 mg in women.[2] These glands are not visible or able to be felt during examination of the neck.[3]

Each parathyroid vein drains into the superior, middle and inferior thyroid veins. The superior and middle thyroid veins drain into the internal jugular vein, and the inferior thyroid vein drains into the brachiocephalic vein.[4]

Lymphatic drainage

Lymphatic vessels from the parathyroid glands drain into deep cervical lymph nodes and paratracheal lymph nodes.[4]

Variation

The parathyroid glands are variable in number: three or more small glands,[5] and can usually be located on the posterior surface of the thyroid gland.[5] Occasionally, some individuals may have six, eight, or even more parathyroid glands.[3] Rarely, the parathyroid glands may be within the thyroid gland itself, the chest, or even the thymus.[5]

Microanatomy

The parathyroid glands are named for their proximity to the thyroid—and serve a completely different role than the thyroid gland. The parathyroid glands are quite easily recognizable from the thyroid as they have densely packed cells, in contrast with the follicular structure of the thyroid.[6] Two unique types of cells are present in the parathyroid gland:

  • Chief cells, which synthesize and release parathyroid hormone. These cells are small, and appear dark when loaded with parathyroid hormone, and clear when the hormone has been secreted, or in their resting state.[7]
  • Oxyphil cells, which are lighter in appearance and increase in number with age,[7] have an unknown function.[8]

Development

In the early development of the human embryo, a series of five pharyngeal arches and four pharyngeal pouches form that give rise to the face, neck, and surrounding structures. The pouches are numbered such that the first pouch is the closest to the top of the embryo's head and the fourth is the furthest from it. The parathyroid glands originate from the interaction of the endoderm of the third and fourth pouch and neural crest mesenchyme.[5] The position of the glands reverses during embryological development. The pair of glands which is ultimately inferior develops from the third pouch with the thymus, whereas the pair of glands which is ultimately superior develops from the fourth pouch. During embryological development, the thymus migrates downwards, dragging the inferior glands with it. The superior pair are not dragged downwards by the fourth pouch to the same degree. The glands are named after their final, not embryological, positions.[9] Since the thymus's ultimate destination is in the mediastinum of the chest, it is occasionally possible to have ectopic parathyroids derived from the third pouch within the chest cavity if they fail to detach in the neck.

Parathyroid development is regulated by a number of genes, including those coding for several transcription factors.[10][a]

Function

See also: Parathyroid hormone

The major function of the parathyroid glands is to maintain the body's calcium and phosphate levels within a very narrow range, so that the nervous and muscular systems can function properly. The parathyroid glands do this by secreting parathyroid hormone (PTH).[11]

Parathyroid hormone (also known as parathormone) is a small protein that takes part in the control of calcium and phosphate homeostasis, as well as bone physiology. Parathyroid hormone has effects antagonistic to those of calcitonin.[12]

  • Calcium. PTH increases blood calcium levels by directly stimulating osteoblasts and thereby indirectly stimulating osteoclasts (through RANK/RANKL mechanism) to break down bone and release calcium. PTH increases gastrointestinal calcium absorption by activating vitamin D, and promotes calcium conservation (reabsorption) by the kidneys.[12]
  • Phosphate. PTH is the major regulator of serum phosphate concentrations via actions on the kidney. It is an inhibitor of proximal tubular reabsorption of phosphorus. Through activation of vitamin D the absorption (intestinal) of Phosphate is increased.[12]

Disorders

Main article: Parathyroid disease

Parathyroid disease is conventionally divided into states where the parathyroid is overactive (hyperparathyroidism), and states where the parathyroid is under- or hypoactive (hypoparathyroidism). Both states are characterised by their symptoms, which relate to the excess or deficiency of parathyroid hormone in the blood.[13]

Hyperparathyroidism

Main article: Hyperparathyroidism

Primary

3D Medical Animation still shot showing Hyperparathyroidism
3D medical animation image showing hyperparathyroidism (right)

Hyperparathyroidism is the state in which there is excess parathyroid hormone circulating in the blood. This may cause bone pain and tenderness, due to increased bone resorption. With increased circulating calcium, there may be other symptoms associated with hypercalcemia, most commonly dehydration. Hyperparathyroidism is most commonly caused by a benign proliferation of chief cells in one parathyroid gland, and rarely in MEN syndrome. This is known as primary hyperparathyroidism,[13] which is generally managed by surgical removal of the abnormal parathyroid gland.[14]

Secondary

Renal disease may lead to hyperparathyroidism. When too much calcium is lost from the blood via urination, there is a compensation by the parathyroid, and parathyroid hormone is released. The glands enlarge (hypertrophy) to synthesize more parathyroid hormone. This is known as secondary hyperparathyroidism.

Tertiary

If secondary hyperparathyroidism persists over months, the parathyroid tissue may become unresponsive to the blood calcium levels, and begin to autonomously release parathyroid hormone. This is known as tertiary hyperparathyroidism.[15]

Hypoparathyroidism

Main article: Hypoparathyroidism

The state of decreased parathyroid activity is known as hypoparathyroidism. This is most commonly associated with damage to the glands or their blood supply during thyroid surgery – it may be associated with rarer genetic syndromes such as DiGeorge syndrome, which is inherited as an autosomal dominant syndrome. Hypoparathyroidism will occur after surgical removal of the parathyroid glands.[16]

Occasionally, an individual's tissues are resistant to the effects of parathyroid hormone. This is known as pseudohypoparathyroidism. In this case the parathyroid glands are fully functional, and the hormone itself is not able to function, resulting in a decrease in blood calcium levels. Pseudohypoparathyroidism is often associated with the genetic condition Albright's hereditary osteodystrophy. Pseudo-pseudohypoparathyroidism, one of the longest words in the English language, is used to describe an individual with Albright's hereditary osteodystrophy with normal parathyroid hormone and serum calcium levels.[16]

Hypoparathyroidism may present with symptoms associated with decreased calcium, and is generally treated with Vitamin D analogues.[16]

History

The parathyroid glands were first discovered in the Indian rhinoceros by Richard Owen in 1852.[17] In his description of the neck anatomy, Owen referred to the glands as "a small compact yellow glandular body attached to the thyroid at the point where the veins emerged". The glands were first discovered in humans by Ivar Viktor Sandström (1852–1889), a Swedish medical student, in 1880 at Uppsala University.[18] Unaware of Owen's description, he described the glands in his monograph "On a New Gland in Man and Fellow Animals" as the "glandulae parathyroidae", noting its existence in dogs, cats, rabbits, oxen, horses and humans.[19][20] For several years, Sandström's description received little attention.[21]

Eugene Gley, Giulio Vassale, and others documented the putative function of the glands in 1891, noting the connection between their removal and the development of muscular tetany. William G. MacCallum in 1908, investigating tumours of the parathyroid, proposed their role in calcium metabolism.[20] He noted that "Tetany occurs spontaneously in many forms and may be produced by the destruction of the parathyroid glands".[22]

The first successful removal of the parathyroid may have been carried out in 1928 by medical doctor Isaac Y Olch, whose intern had noticed elevated calcium levels in an elderly patient with muscle weakness. Prior to this surgery, patients with removed parathyroid glands typically died from muscular tetany.[20]

Parathyroid hormone was isolated in 1923 by Adolph M. Hanson and 1925 by James B. Collip. Studies of parathyroid hormone levels by Roger Guillemin, Andrew Schally and Rosalyn Sussman Yalow led to the development of immunoassays capable of measuring body substances and a Nobel Prize in 1977.[18][20]

Other animals

Parathyroid glands are found in all adult tetrapods; they vary in their number and position. Mammals typically have four parathyroid glands, while other types of animals typically have six. The removal of parathyroid glands in animals produces a condition resembling acute poisoning with irregular muscle contractions.[23]

Fish do not possess parathyroid glands; several species have been found to express parathyroid hormone. Developmental genes and calcium-sensing receptors in fish gills are similar to those within the parathyroid glands of birds and mammals. It has been suggested that the tetrapod glands may have been evolutionarily derived from these fish gills.[10][24]

Additional images

  • Gross pathology of a parathyroid gland (white arrow), next to the thyroid gland
    Gross pathology of a parathyroid gland (white arrow), next to the thyroid gland
  • Scheme showing development of branchial epithelial bodies. I, II, III, IV. Branchial pouches.
    Scheme showing development of branchial epithelial bodies. I, II, III, IV. Branchial pouches.

See also

Notes

  1. ^ Namely the co-activator EYA1, the homeobox transcription factor SIX1, and the transcription factor GCM2[10]

References

  1. ^ Gray, Henry (1980). Williams, Peter L; Warwick, Roger (eds.). Gray's Anatomy (36th ed.). Churchill Livingstone. p. 1453. ISBN 0-443-01505-8.
  2. ^ Johnson, S J (1 April 2005). "Best Practice No 183: Examination of parathyroid gland specimens". Journal of Clinical Pathology. 58 (4): 338–342. doi:10.1136/jcp.2002.002550. PMC 1770637. PMID 15790694.
  3. ^ a b Illustrated Anatomy of the Head and Neck, Fehrenbach and Herring, Elsevier, 2012, p. 159
  4. ^ a b Drake, Richard L.; Vogl, Wayne; Tibbitts, Adam W.M. Mitchell; illustrations by Richard; Richardson, Paul (2005). Gray's anatomy for students. Philadelphia: Elsevier/Churchill Livingstone. p. 918. ISBN 978-0-8089-2306-0.
  5. ^ a b c d Williams, S. Jacob; dissections by David J. Hinchcliffe; photography by Mick A. Turton; illustrated by Amanda (2007). Human anatomy: a clinically-orientated approach (New ed.). Edinburgh: Churchill Livingstone. ISBN 978-0-443-10373-5.{{cite book}}: CS1 maint: multiple names: authors list (link)[page needed]
  6. ^ Lappas D, Noussios G, Anagnostis P, Adamidou F, Chatzigeorgiou A, Skandalakis P (September 2012). "Location, number and morphology of parathyroid glands: results from a large anatomical series". Anat Sci Int. 87 (3): 160–4. doi:10.1007/s12565-012-0142-1. PMID 22689148. S2CID 207431255.
  7. ^ a b c Young, Barbara; Heath, John W.; Stevens, Alan; Burkitt, H. George (2006). Wheater's functional histology: a text and colour atlas (5th ed.). Edinburgh: Churchill Livingstone/Elsevier. p. 337. ISBN 978-0-443-06850-8.
  8. ^ Ritter, Cynthia S.; Haughey, Bruce H.; Miller, Brent; Brown, Alex J. (August 2012). "Differential Gene Expression by Oxyphil and Chief Cells of Human Parathyroid Glands". The Journal of Clinical Endocrinology & Metabolism. 97 (8): E1499–E1505. doi:10.1210/jc.2011-3366. PMC 3591682. PMID 22585091.
  9. ^ Larsen, William J. (2001). Human embryology (3rd ed.). Philadelphia, Pa.: Churchill Livingstone. pp. 377–8. ISBN 0-443-06583-7.
  10. ^ a b c Zajac, Jeffrey D; Danks, Janine A (July 2008). "The development of the parathyroid gland: from fish to human". Current Opinion in Nephrology and Hypertension. 17 (4): 353–356. doi:10.1097/MNH.0b013e328304651c. PMID 18660669. S2CID 7971353.
  11. ^ Young, Barbara; Heath, John W.; Stevens, Alan; Burkitt, H. George (2006). Wheater's functional histology: a text and colour atlas (5th ed.). Edinburgh: Churchill Livingstone/Elsevier. p. 336. ISBN 978-0-443-06850-8.
  12. ^ a b c Hall, Arthur C. Guyton, John E. (2005). Textbook of medical physiology (11th ed.). Philadelphia: W.B. Saunders. pp. 985–8. ISBN 978-0-7216-0240-0.{{cite book}}: CS1 maint: multiple names: authors list (link)
  13. ^ a b Colledge, Nicki R.; Walker, Brian R.; Ralston, Stuart H., eds. (2010). Davidson's principles and practice of medicine (21st ed.). Edinburgh: Churchill Livingstone/Elsevier. pp. 766–7. ISBN 978-0-7020-3084-0.
  14. ^ Colledge, Nicki R.; Walker, Brian R.; Ralston, Stuart H., eds. (2010). Davidson's principles and practice of medicine (21st ed.). Edinburgh: Churchill Livingstone/Elsevier. p. 767. ISBN 978-0-7020-3084-0.
  15. ^ Staren, Prinz; Richard, A., eds. (2000). Endocrine surgery. Georgetown TX: Landes Bioscience. pp. 98–114. ISBN 978-1-57059-574-5.
  16. ^ a b c Colledge, Nicki R.; Walker, Brian R.; Ralston, Stuart H., eds. (2010). Davidson's principles and practice of medicine (21st ed.). Edinburgh: Churchill Livingstone/Elsevier. p. 768. ISBN 978-0-7020-3084-0.
  17. ^ Cave, A.J.E. (1953). "Richard Owen and the discovery of the parathyroid glands" (PDF). In E. Ashworth Underwood (ed.). Science, Medicine and History. Essays on the Evolution of Scientific Thought and Medical Practice. Vol. 2. Oxford University Press. pp. 217–222. Retrieved 2009-07-20.
  18. ^ a b Eknoyan G (November 1995). "A history of the parathyroid glands". American Journal of Kidney Diseases. 26 (5): 801–7. doi:10.1016/0272-6386(95)90447-6. PMID 7485136.
  19. ^ "On a New Gland in Man and Several Mammals (Glandulæ Parathyreoideæ)". Journal of the American Medical Association. 111 (2): 197. 9 July 1938. doi:10.1001/jama.1938.02790280087037.
  20. ^ a b c d DuBose, Joseph; Ragsdale, Timothy; Morvant, Jason (January 2005). ""Bodies so tiny": The history of parathyroid surgery". Current Surgery. 62 (1): 91–95. doi:10.1016/j.cursur.2004.07.012. PMID 15708157.
  21. ^ Carney, JA (Sep 1996). "The glandulae parathyroideae of Ivar Sandström. Contributions from two continents". The American Journal of Surgical Pathology. 20 (9): 1123–44. doi:10.1097/00000478-199609000-00010. PMID 8764749.
  22. ^ Maccallum, W. G; Voegtlin, C. (Jan 9, 1909). "On the Relation of Tetant to the Parathyroid Glands and to Calcium Metabolism". The Journal of Experimental Medicine. 11 (1): 118–51. doi:10.1084/jem.11.1.118. PMC 2124703. PMID 19867238.
  23. ^ Councilman, WT (1913). "Chapter 1". Disease and Its Causes. United States: New York Henry Holt and Company London Williams and Norgate The University Press, Cambridge, U.S. ASIN B0065T4O6Q. OCLC 654587300.
  24. ^ Okabe, Masataka; Graham, Anthony (2004). "The origin of the parathyroid gland". Proceedings of the National Academy of Sciences. 101 (51): 17716–9. Bibcode:2004PNAS..10117716O. doi:10.1073/pnas.0406116101. JSTOR 3374034. PMC 539734. PMID 15591343.

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