Hamartoma risk factors: Difference between revisions
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==Overview== | ==Overview== | ||
The most potent risk factor in the development of hamartomas is familial hamartomatous syndromes.<ref name="pmid26739631">{{cite journal |vauthors=Richardson MS |title=Familiar and unfamiliar pseudoneoplastic lesions of the head and neck |journal=Semin Diagn Pathol |volume=33 |issue=1 |pages=24–30 |year=2016 |pmid=26739631 |doi=10.1053/j.semdp.2015.09.004 |url=}}</ref> | The most potent risk factor in the development of hamartomas is familial hamartomatous syndromes.<ref name="pmid26739631">{{cite journal |vauthors=Richardson MS |title=Familiar and unfamiliar pseudoneoplastic lesions of the head and neck |journal=Semin Diagn Pathol |volume=33 |issue=1 |pages=24–30 |year=2016 |pmid=26739631 |doi=10.1053/j.semdp.2015.09.004 |url=}}</ref> | ||
==Risk factors== | ==Risk factors== | ||
Revision as of 17:58, 26 January 2016
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Maria Fernanda Villarreal, M.D. [2]
Overview
The most potent risk factor in the development of hamartomas is familial hamartomatous syndromes.[1]
Risk factors
- The most potent risk factor in the development of hamartomas is familial hamartomatous syndromes.
- Risk factors associated with hamartomatous formation, include:[2]
- Juvenile polyposis syndrome
- Peutz-Jeghers syndrome
- Hereditary mixed polyposis syndrome
- PTEN hamartoma tumour syndrome
- Tuberous sclerosis
- Cowden’s syndrome
- Bannayan-Riley-Ruvalcaba syndrome
References
- ↑ Richardson MS (2016). "Familiar and unfamiliar pseudoneoplastic lesions of the head and neck". Semin Diagn Pathol. 33 (1): 24–30. doi:10.1053/j.semdp.2015.09.004. PMID 26739631.
- ↑ Liaw D, Marsh DJ, Li J, Dahia PL, Wang SI, Zheng Z; et al. (1997). "Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome". Nat Genet. 16 (1): 64–7. doi:10.1038/ng0597-64. PMID 9140396.