Prolactinoma causes: Difference between revisions
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__NOTOC__ | __NOTOC__ | ||
{{Prolactinoma}} | {{Prolactinoma}} | ||
{{CMG}} {{AE}}{{ | {{CMG}} {{AE}}{{Anmol}} | ||
==Overview== | ==Overview== | ||
There are no established causes for prolactinoma. Most [[ | There are no established causes for [[prolactinoma]]. Most cases of [[prolactinoma]] are [[sporadic]]. | ||
==Causes== | ==Causes== | ||
There are no established causes for prolactinoma. Most | There are no established causes for [[prolactinoma]]. Most cases of [[prolactinoma]] are [[sporadic]]. [[Prolactinoma]] may occur in approximately 30% of [[Multiple endocrine neoplasia type 1]].It may also occur with [[Carney complex]] or [[McCune-Albright syndrome]].<ref name="pmid16411062">{{cite journal| author=Ciccarelli A, Daly AF, Beckers A| title=The epidemiology of prolactinomas. | journal=Pituitary | year= 2005 | volume= 8 | issue= 1 | pages= 3-6 | pmid=16411062 | doi=10.1007/s11102-005-5079-0 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16411062 }} </ref> | ||
===Familial Causes=== | ===Familial Causes<ref name="pmid16411062">{{cite journal| author=Ciccarelli A, Daly AF, Beckers A| title=The epidemiology of prolactinomas. | journal=Pituitary | year= 2005 | volume= 8 | issue= 1 | pages= 3-6 | pmid=16411062 | doi=10.1007/s11102-005-5079-0 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16411062 }} </ref><ref name="pmid17613551">{{cite journal| author=Karhu A, Aaltonen LA| title=Susceptibility to pituitary neoplasia related to MEN-1, CDKN1B and AIP mutations: an update. | journal=Hum Mol Genet | year= 2007 | volume= 16 Spec No 1 | issue= | pages= R73-9 | pmid=17613551 | doi=10.1093/hmg/ddm036 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17613551 }} </ref>=== | ||
[[Prolactinoma]] may occur as part of a hereditary disorder called [[multiple endocrine neoplasia type 1]] ([[MEN 1]]). A minority of | [[Prolactinoma]] may occur as part of a [[hereditary disorder]] called [[multiple endocrine neoplasia type 1]] ([[MEN 1]]). A minority of [[prolactinoma]] are associated with: | ||
*[[Carney complex]] | *[[Carney complex]] | ||
*[[McCune-Albright Syndrome]] | *[[McCune-Albright Syndrome]] | ||
* | *Isolated [[familial]] [[pituitary adenoma]] | ||
=== Other Causes === | === Other Causes === | ||
Other causes include: | Other causes include: | ||
*The xenoestrogenic chemical Bisphenol-A has been demonstrated to result in [[hyperprolactinaemia]] and growth of prolactin-producing pituitary cells.<ref>^ Goloubkova T, Ribeiro MF, Rodrigues LP, Cecconello AL, Spritzer PM (April 2000). "Effects of xenoestrogen bisphenol A on uterine and pituitary weight, serum prolactin levels and immunoreactive prolactin cells in ovariectomized Wistar rats". Arch. Toxicol. 74 (2): 92–8. doi:10.1007/s002040050658. PMID 10839476</ref> The increasing and prolonged exposure of Bisphenol-A from childhood may contribute to the development and growth of a [[prolactinoma]]. | *The xenoestrogenic chemical Bisphenol-A has been demonstrated to result in [[hyperprolactinaemia]] and growth of [[Lactotroph|prolactin-producing pituitary cells]].<ref>^ Goloubkova T, Ribeiro MF, Rodrigues LP, Cecconello AL, Spritzer PM (April 2000). "Effects of xenoestrogen bisphenol A on uterine and pituitary weight, serum prolactin levels and immunoreactive prolactin cells in ovariectomized Wistar rats". Arch. Toxicol. 74 (2): 92–8. doi:10.1007/s002040050658. PMID 10839476</ref> The increasing and prolonged exposure of Bisphenol-A from childhood may contribute to the development and growth of a [[prolactinoma]]. | ||
== References == | == References == | ||
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Anmol Pitliya, M.B.B.S. M.D.[2]
Overview
There are no established causes for prolactinoma. Most cases of prolactinoma are sporadic.
Causes
There are no established causes for prolactinoma. Most cases of prolactinoma are sporadic. Prolactinoma may occur in approximately 30% of Multiple endocrine neoplasia type 1.It may also occur with Carney complex or McCune-Albright syndrome.[1]
Familial Causes[1][2]
Prolactinoma may occur as part of a hereditary disorder called multiple endocrine neoplasia type 1 (MEN 1). A minority of prolactinoma are associated with:
Other Causes
Other causes include:
- The xenoestrogenic chemical Bisphenol-A has been demonstrated to result in hyperprolactinaemia and growth of prolactin-producing pituitary cells.[3] The increasing and prolonged exposure of Bisphenol-A from childhood may contribute to the development and growth of a prolactinoma.
References
- ↑ 1.0 1.1 Ciccarelli A, Daly AF, Beckers A (2005). "The epidemiology of prolactinomas". Pituitary. 8 (1): 3–6. doi:10.1007/s11102-005-5079-0. PMID 16411062.
- ↑ Karhu A, Aaltonen LA (2007). "Susceptibility to pituitary neoplasia related to MEN-1, CDKN1B and AIP mutations: an update". Hum Mol Genet. 16 Spec No 1: R73–9. doi:10.1093/hmg/ddm036. PMID 17613551.
- ↑ ^ Goloubkova T, Ribeiro MF, Rodrigues LP, Cecconello AL, Spritzer PM (April 2000). "Effects of xenoestrogen bisphenol A on uterine and pituitary weight, serum prolactin levels and immunoreactive prolactin cells in ovariectomized Wistar rats". Arch. Toxicol. 74 (2): 92–8. doi:10.1007/s002040050658. PMID 10839476