Prolactinoma causes: Difference between revisions
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{{CMG}} {{AE}}{{Anmol}} | {{CMG}} {{AE}}{{Anmol}} | ||
==Overview== | ==Overview== | ||
There are no established causes for [[prolactinoma]]. Most cases of [[prolactinoma]] are | There are no established causes for [[prolactinoma]]. Most cases of [[prolactinoma]] are sporadic. | ||
==Causes== | ==Causes== | ||
There are no established causes for [[prolactinoma]]. Most cases of [[prolactinoma]] are | 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> | ||
===Common causes=== | |||
*Sporadic | |||
*[[Hereditary]] causes: | |||
**[[Multiple endocrine neoplasia type 1]] ([[MEN 1]]) | |||
=== | ===Less Common/Rare causes=== | ||
*[[Hereditary]] causes: | |||
**A minority of [[prolactinoma]] are associated with:<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> | |||
*[[Carney complex]] | **#[[Carney complex]] | ||
*[[McCune-Albright Syndrome]] | **#[[McCune-Albright Syndrome]] | ||
*Isolated [[familial]] [[pituitary adenoma]] | **#Isolated [[familial]] [[pituitary adenoma]] | ||
== References == | == References == |
Revision as of 20:38, 19 July 2017
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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]
Common causes
- Sporadic
- Hereditary causes:
Less Common/Rare causes
- Hereditary causes:
- A minority of prolactinoma are associated with:[1][2]
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.