Hereditary nonpolyposis colorectal cancer classification: Difference between revisions
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::*Genes affected are [[MLH1]], [[MSH2]], and more recently, MSH6, and are involved in [[DNA mismatch repair]] | ::*Genes affected are [[MLH1]], [[MSH2]], and more recently, MSH6, and are involved in [[DNA mismatch repair]] | ||
'''Turcot syndrome'''<ref name="pmid28256262">{{cite journal| author=Velter C, Caussade P, Fricker JP, Cribier B| title=[Muir-Torre syndrome and Turcot syndrome]. | journal=Ann Dermatol Venereol | year= 2017 | volume= 144 | issue= 8-9 | pages= 525-529 | pmid=28256262 | doi=10.1016/j.annder.2017.01.017 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28256262 }} </ref> | '''Turcot syndrome'''<ref name="pmid28256262">{{cite journal| author=Velter C, Caussade P, Fricker JP, Cribier B| title=[Muir-Torre syndrome and Turcot syndrome]. | journal=Ann Dermatol Venereol | year= 2017 | volume= 144 | issue= 8-9 | pages= 525-529 | pmid=28256262 | doi=10.1016/j.annder.2017.01.017 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28256262 }} </ref><ref name="pmid23119205">{{cite journal| author=Dipro S, Al-Otaibi F, Alzahrani A, Ulhaq A, Al Shail E| title=Turcot syndrome: a synchronous clinical presentation of glioblastoma multiforme and adenocarcinoma of the colon. | journal=Case Rep Oncol Med | year= 2012 | volume= 2012 | issue= | pages= 720273 | pmid=23119205 | doi=10.1155/2012/720273 | pmc=3479943 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23119205 }} </ref> | ||
::*Hereditary [[autosomal recessive]] syndrome | ::*Hereditary [[autosomal recessive]] syndrome | ||
::*Considered a subtype of hereditary nonpolyposis colorectal cancer | ::*Considered a subtype of hereditary nonpolyposis colorectal cancer |
Revision as of 05:17, 11 February 2019
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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]Ali Akram, M.B.B.S.[3]
Overview
Hereditary nonpolyposis colorectal cancer may be classified into 2 types: Lynch syndrome I (familial colon cancer) and Lynch syndrome II (hereditary nonpolyposis colorectal cancer associated with other cancers).
Classification
Lynch Syndrome I (Familial Colon Cancer)
- Site-specific colonic cancer
Lynch Syndrome II
- Includes extracolonic cancer.
- The most common cancer that develop among such patients is endometrial carcinoma
Variants
- Hereditary autosomal dominant syndrome
- Considered a subtype of hereditary nonpolyposis colorectal cancer
- Individuals are prone to develop cancers of the colon, breast, and genitourinary tract, and skin lesions, such as keratoacanthomas and sebaceous tumors
- Genes affected are MLH1, MSH2, and more recently, MSH6, and are involved in DNA mismatch repair
- Hereditary autosomal recessive syndrome
- Considered a subtype of hereditary nonpolyposis colorectal cancer
- Individuals are prone to develop intestinal polyposis in addition to CNS tumors such as glioblastoma or medulloblastoma
- Two-thirds of patients have mutations in the APC gene
References
- ↑ Mintsoulis D, Beecker J (2016). "Muir-Torre syndrome". CMAJ. 188 (5): E95. doi:10.1503/cmaj.150171. PMC 4786404. PMID 26527831.
- ↑ John AM, Schwartz RA (2016). "Muir-Torre syndrome (MTS): An update and approach to diagnosis and management". J Am Acad Dermatol. 74 (3): 558–66. doi:10.1016/j.jaad.2015.09.074. PMID 26892655.
- ↑ 3.0 3.1 Velter C, Caussade P, Fricker JP, Cribier B (2017). "[Muir-Torre syndrome and Turcot syndrome]". Ann Dermatol Venereol. 144 (8–9): 525–529. doi:10.1016/j.annder.2017.01.017. PMID 28256262.
- ↑ Dipro S, Al-Otaibi F, Alzahrani A, Ulhaq A, Al Shail E (2012). "Turcot syndrome: a synchronous clinical presentation of glioblastoma multiforme and adenocarcinoma of the colon". Case Rep Oncol Med. 2012: 720273. doi:10.1155/2012/720273. PMC 3479943. PMID 23119205.