Prolactinoma pathophysiology: Difference between revisions
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*McCune-Albright Syndrome | *McCune-Albright Syndrome | ||
*MEN like syndrome ( CKDN1B loss of function)<ref>http://radiopaedia.org/articles/pituitary-adenoma</ref> | *MEN like syndrome ( CKDN1B loss of function)<ref>http://radiopaedia.org/articles/pituitary-adenoma</ref> | ||
====Familial pituitary adenomas==== | |||
A pituitary adenoma may be part of a familial syndrome:<ref name=pmid19564887>{{Cite journal | last1 = Elston | first1 = MS. | last2 = McDonald | first2 = KL. | last3 = Clifton-Bligh | first3 = RJ. | last4 = Robinson | first4 = BG. | title = Familial pituitary tumor syndromes. | journal = Nat Rev Endocrinol | volume = 5 | issue = 8 | pages = 453-61 | month = Aug | year = 2009 | doi = 10.1038/nrendo.2009.126 | PMID = 19564887 }}</ref><ref name=Ref_PCPBoD8|554>{{Ref PCPBoD8|554}}</ref> | |||
{| class="wikitable sortable" style="margin-left:auto;margin-right:auto" | |||
! Syndrome | |||
! Gene | |||
! Notes | |||
|- | |||
| [[Multiple endocrine neoplasia]] I | |||
| MEN1 | |||
| characterized by the 3 Ps: '''p'''ituitary adenoma, [[parathyroid adenoma|'''p'''arathyroid adenoma]], [[pancreatic neuroendocrine tumour|'''p'''ancreatic neuroendocrine tumour]] | |||
|- | |||
| MEN-1-like syndrome | |||
| CDKN1B<ref name=omim600778>{{OMIM|600778}}</ref> | |||
| also known as ''Multiple endocrine neoplasia IV'' <ref name=omim600778>{{OMIM|600778}}</ref> | |||
|- | |||
| [[Carney syndrome]] | |||
| PRKAR1A | |||
| other findings (mnemonic ''NAME''): nevi, [[atrial myxoma]], myxoid neurofibroma, ephelides (freckles) | |||
|- | |||
| Isolated pituitary adenoma<ref name=pmid22612670>{{Cite journal | last1 = Korbonits | first1 = M. | last2 = Storr | first2 = H. | last3 = Kumar | first3 = AV. | title = Familial pituitary adenomas - Who should be tested for AIP mutations? | journal = Clin Endocrinol (Oxf) | volume = | issue = | pages = | month = May | year = 2012 | doi = 10.1111/j.1365-2265.2012.04445.x | PMID = 22612670 }}</ref> | |||
| AIP | |||
| classically GH-producing adenoma - leads to acromegaly | |||
|} | |||
===Microscopic=== | |||
Features:<ref name=Ref_PSNP36>{{Ref PSNP|36}}</ref> | |||
*Loss of fibrous stroma. | |||
**The cells of a normal (anterior) pituitary are nested. | |||
Notes: | |||
*Smears very well.<ref>MUN. 24 November 2010.</ref> | |||
====Images==== | |||
<gallery> | |||
Image:Nonfunctioning_pituitary_adenoma_%281%29.jpg | Pituitary adenoma - non-functioning. (WC/KGH) | |||
File:HE fibrosis pituitary adenoma.jpg | Extensive interstitial and perivascular fibrosis in a pituitary adenoma (WC/jensflorian) | |||
File:PRL HE histology.jpg | Pituitary adenoma - PRL producing, HE. Note the basophilic appearance of the cells (WC/jensflorian) | |||
File:PRL adenoma treatment HE.jpg | Pituitary adenoma - PRL producing, HE. Extensive regressive changes after after dopamine agonist treatment (WC/jensflorian) | |||
File:PRL IHC pituitary adenoma.jpg | Pituitary adenoma - PRL producing, Prolactin IHC (WC/jensflorian) | |||
File:Densely granulated HGH producing adenoma.jpg | Pituitary adenoma - HGH producing, HE. The cells have a slightly eosinophilic appearance (WC/jensflorian) | |||
File:Sparsely granulated HGH adenoma.jpg | Sparsely granulated adenoma - HGH producing. Note the numerous fibrous bodies in HE stain (WC/jensflorian) | |||
File:HGH adenoma CK8.jpg | Sparsely granulated adenoma - HGH producing. CK8 IHC highlighting fibrous bodies (WC/jensflorian) | |||
File:TSHoma HE.jpg | Pituitary adenoma - TSH producing. HE stain showing pleomorphism (WC/jensflorian) | |||
File:TSHoma IHC-TSH.jpg | Pituitary adenoma - TSH producing. TSH IHC can be heterogeneous (WC/jensflorian) | |||
Image:Pituitary_adenoma_%281%29_GH_production.jpg | Pituitary adenoma - GH producing. (WC/KGH) | |||
File:HE-GHoma.jpg | Pituitary adenoma , HE. This gonadotropin producing adenoma has a papillary architecture (WC/jensflorian) | |||
File:FSH-GHoma.jpg | Pituitary adenoma, IHC for FSH (WC/jensflorian) | |||
File:LH-GHoma.jpg | Pituitary adenoma, IHC for LH (WC/jensflorian) | |||
File:ACTHoma-PAS-O-G.jpg | Pituitary adenoma , ACTH producing. PAS-O-G stain showing basophilic adenoma cells (WC/jensflorian) | |||
File:ACTHoma-IHC.jpg | Pituitary adenoma , ACTH producing. Strong ACTH IHC in this basophilic adenoma (WC/jensflorian) | |||
</gallery> | |||
www: | |||
*[http://path.upmc.edu/cases/case6.html Pituitary adenoma - crappy pictures (upmc.edu)]. | |||
*[http://path.upmc.edu/cases/case556.html Pituitary adenoma - case 2 - several images (upmc.edu)]. | |||
===Stains=== | |||
*Reticulin - loss of reticulin between tumour cells. | |||
== References == | == References == |
Revision as of 17:38, 9 September 2015
Prolactinoma Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Prolactinoma pathophysiology On the Web |
American Roentgen Ray Society Images of Prolactinoma pathophysiology |
Risk calculators and risk factors for Prolactinoma pathophysiology |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Faizan Sheraz, M.D. [2]
Overview
Prolactinoma may occur as part of a hereditary disorder called multiple endocrine neoplasia type 1 (MEN 1). A minority of prolactinomas are associated with multiple endocrine neoplasia type I (MEN I), Carney complex, McCune-Albright Syndrome, MEN like syndrome ( CKDN1B loss of function).[1]
Pathophysiology
Prolactinoma may occur as part of a hereditary disorder called multiple endocrine neoplasia type 1 (MEN 1). A minority of prolactinomas are associated with:
- Multiple endocrine neoplasia type I (MEN I)
- Carney complex
- McCune-Albright Syndrome
- MEN like syndrome ( CKDN1B loss of function)[2]
Familial pituitary adenomas
A pituitary adenoma may be part of a familial syndrome:[3][4]
Syndrome | Gene | Notes |
---|---|---|
Multiple endocrine neoplasia I | MEN1 | characterized by the 3 Ps: pituitary adenoma, parathyroid adenoma, pancreatic neuroendocrine tumour |
MEN-1-like syndrome | CDKN1B[5] | also known as Multiple endocrine neoplasia IV [5] |
Carney syndrome | PRKAR1A | other findings (mnemonic NAME): nevi, atrial myxoma, myxoid neurofibroma, ephelides (freckles) |
Isolated pituitary adenoma[6] | AIP | classically GH-producing adenoma - leads to acromegaly |
Microscopic
Features:[7]
- Loss of fibrous stroma.
- The cells of a normal (anterior) pituitary are nested.
Notes:
- Smears very well.[8]
Images
-
Pituitary adenoma - non-functioning. (WC/KGH)
-
Extensive interstitial and perivascular fibrosis in a pituitary adenoma (WC/jensflorian)
-
Pituitary adenoma - PRL producing, HE. Note the basophilic appearance of the cells (WC/jensflorian)
-
Pituitary adenoma - PRL producing, HE. Extensive regressive changes after after dopamine agonist treatment (WC/jensflorian)
-
Pituitary adenoma - PRL producing, Prolactin IHC (WC/jensflorian)
-
Pituitary adenoma - HGH producing, HE. The cells have a slightly eosinophilic appearance (WC/jensflorian)
-
Sparsely granulated adenoma - HGH producing. Note the numerous fibrous bodies in HE stain (WC/jensflorian)
-
Sparsely granulated adenoma - HGH producing. CK8 IHC highlighting fibrous bodies (WC/jensflorian)
-
Pituitary adenoma - TSH producing. HE stain showing pleomorphism (WC/jensflorian)
-
Pituitary adenoma - TSH producing. TSH IHC can be heterogeneous (WC/jensflorian)
-
Pituitary adenoma - GH producing. (WC/KGH)
-
Pituitary adenoma , HE. This gonadotropin producing adenoma has a papillary architecture (WC/jensflorian)
-
Pituitary adenoma, IHC for FSH (WC/jensflorian)
-
Pituitary adenoma, IHC for LH (WC/jensflorian)
-
Pituitary adenoma , ACTH producing. PAS-O-G stain showing basophilic adenoma cells (WC/jensflorian)
-
Pituitary adenoma , ACTH producing. Strong ACTH IHC in this basophilic adenoma (WC/jensflorian)
www:
- Pituitary adenoma - crappy pictures (upmc.edu).
- Pituitary adenoma - case 2 - several images (upmc.edu).
Stains
- Reticulin - loss of reticulin between tumour cells.
References
- ↑ http://radiopaedia.org/articles/pituitary-adenoma
- ↑ http://radiopaedia.org/articles/pituitary-adenoma
- ↑ Elston, MS.; McDonald, KL.; Clifton-Bligh, RJ.; Robinson, BG. (2009). "Familial pituitary tumor syndromes". Nat Rev Endocrinol. 5 (8): 453–61. doi:10.1038/nrendo.2009.126. PMID 19564887. Unknown parameter
|month=
ignored (help) - ↑ Template:Ref PCPBoD8
- ↑ 5.0 5.1 Online Mendelian Inheritance in Man (OMIM) 600778
- ↑ Korbonits, M.; Storr, H.; Kumar, AV. (2012). "Familial pituitary adenomas - Who should be tested for AIP mutations?". Clin Endocrinol (Oxf). doi:10.1111/j.1365-2265.2012.04445.x. PMID 22612670. Unknown parameter
|month=
ignored (help) - ↑ Template:Ref PSNP
- ↑ MUN. 24 November 2010.