Difference between revisions of "Multiple endocrine neoplasia"
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Memory device: '''3 Ps'''. | Memory device: '''3 Ps'''. | ||
===MEN 2A | ===MEN 2A (II)=== | ||
* Parathyroid adenoma. | * Parathyroid adenoma. | ||
* [[Medullary thyroid carcinoma]] (usu. preceded by C cell hyperplasia<ref name=Ref_PBoD8_1162>{{Ref PBoD8|1162}}}}</ref>). | * [[Medullary thyroid carcinoma]] (usu. preceded by C cell hyperplasia<ref name=Ref_PBoD8_1162>{{Ref PBoD8|1162}}}}</ref>). | ||
* [[Pheochromocytoma]]. | * [[Pheochromocytoma]]. | ||
Notes: | Notes - memory device: | ||
* | *Both MEN 1 and MEN 2A have parathyroid adenomas. | ||
* | *Each has additional neoplasms below ''and'' above the diaphragm. | ||
===MEN 3A (III)=== | |||
* Neuromas/[[ganglioneuroma]]s. | |||
* [[Medullary thyroid carcinoma]] (usu. preceded by C cell hyperplasia<ref name=Ref_PBoD8_1162>{{Ref PBoD8|1162}}}}</ref>). | |||
* [[Pheochromocytoma]]. | |||
==Details== | ==Details== | ||
Revision as of 21:19, 19 March 2011
Multiple endocrine neoplasia, abbreviated MEN, refers to collection of different genetic abnormalities that lead to endocrine neoplasms.
Simple
MEN 1
- Parathyroid adenoma.[1]
- Pancreatic neuroendocrine tumours.
- Pituitary adenoma.
Memory device: 3 Ps.
MEN 2A (II)
- Parathyroid adenoma.
- Medullary thyroid carcinoma (usu. preceded by C cell hyperplasia[2]).
- Pheochromocytoma.
Notes - memory device:
- Both MEN 1 and MEN 2A have parathyroid adenomas.
- Each has additional neoplasms below and above the diaphragm.
MEN 3A (III)
- Neuromas/ganglioneuromas.
- Medullary thyroid carcinoma (usu. preceded by C cell hyperplasia[2]).
- Pheochromocytoma.
Details
MEN 1
Characteristics:[2]
- Endocrine tumours usu. lead to most of the morbidity.
- Usu. arise in the duodenum.
- Zollinger-Ellison syndrome is common.
- Usu. arise in the duodenum.
MEN 2A
Characteristics:[2]
- Medullary thyroid carcinoma - in almost 100%.
Images:
Trivia:
- In MEN 2A and 2B the RET gene is abnormally activated. In Hirschsprung disease, it is inactivated.[2]
MEN 2B
Characteristics:
- Marfanoid habitus.[3]
- Neuromas.
- Ganglioneuromatosis of the alimentary tract.[4][5]
- Extra large nerves in GI tract.
References
- ↑ URL: http://www.pathconsultddx.com/pathCon/diagnosis?pii=S1559-8675%2806%2970475-2. Accessed on: 2 September 2010.
- ↑ 2.0 2.1 2.2 2.3 2.4 Kumar, Vinay; Abbas, Abul K.; Fausto, Nelson; Aster, Jon (2009). Robbins and Cotran pathologic basis of disease (8th ed.). Elsevier Saunders. pp. 1162. ISBN 978-1416031215. }}
- ↑ Kumar, Vinay; Abbas, Abul K.; Fausto, Nelson; Aster, Jon (2009). Robbins and Cotran pathologic basis of disease (8th ed.). Elsevier Saunders. pp. 1160. ISBN 978-1416031215. }}
- ↑ URL: http://www.ncbi.nlm.nih.gov/omim/162300. Accessed on: 19 November 2010.
- ↑ Haraguchi M, Kinoshita H, Koori M, et al. (2007). "Multiple rectal carcinoids with diffuse ganglioneuromatosis". World J Surg Oncol 5: 19. doi:10.1186/1477-7819-5-19. PMC 1805501. PMID 17306015. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1805501/.