Acinic cell carcinoma risk factors: Difference between revisions

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==Risk Factors==
==Risk Factors==
There are no established risk factors for [disease name].
Common risk factors in the development of acinic cell carcinoma include:
 
OR
 
The most potent risk factor in the development of [disease name] is [risk factor 1]. Other risk factors include [risk factor 2], [risk factor 3], and [risk factor 4].
 
OR
 
Common risk factors in the development of [disease name] include [risk factor 1], [risk factor 2], [risk factor 3], and [risk factor 4].
===Common Risk Factors===
===Common Risk Factors===
*Common risk factors in the development of [disease name] may be occupational, environmental, genetic, and viral.
*Common risk factors in the development of acinic cell carcinoma may be occupational, environmental, genetic<ref name="pmid9118025">{{cite journal| author=Saku T, Hayashi Y, Takahara O, Matsuura H, Tokunaga M, Tokunaga M et al.| title=Salivary gland tumors among atomic bomb survivors, 1950-1987. | journal=Cancer | year= 1997 | volume= 79 | issue= 8 | pages= 1465-75 | pmid=9118025 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9118025  }}</ref><ref name="pmid10539921">{{cite journal| author=Depowski PL, Setzen G, Chui A, Koltai PJ, Dollar J, Ross JS| title=Familial occurrence of acinic cell carcinoma of the parotid gland. | journal=Arch Pathol Lab Med | year= 1999 | volume= 123 | issue= 11 | pages= 1118-20 | pmid=10539921 | doi=10.1043/0003-9985(1999)123<1118:FOOACC>2.0.CO;2 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10539921  }}</ref><ref name="VilleneuveTremblay2011">{{cite journal|last1=Villeneuve|first1=Hugo|last2=Tremblay|first2=Steve|last3=Galiatsatos|first3=Polymnia|last4=Hamel|first4=Nancy|last5=Guertin|first5=Louis|last6=Morency|first6=Renald|last7=Tischkowitz|first7=Marc|title=Acinic cell carcinoma of the retromolar trigone region: expanding the tumor phenotype in Cowden syndrome?|journal=Familial Cancer|volume=10|issue=4|year=2011|pages=691–694|issn=1389-9600|doi=10.1007/s10689-011-9472-8}}</ref>.
*Common risk factors in the development of [disease name] include:
*Common risk factors in the development of acinic cell carcinoma include:
**[Risk factor 1]
**Familial predisposition
**[Risk factor 2]
**Previous radiation exposure
**[Risk factor 3]
**[[Cowden syndrome]]
 
**Acinic breast cancer may develop in a [[BRCA1]] mutation carrier
===Less Common Risk Factors===
**There were no cases among long-term atomic bomb survivors
*Less common risk factors in the development of [disease name] include:
**[Risk factor 1]
**[Risk factor 2]
**[Risk factor 3]
 
==Risk Factors==
There is very little known about acinic cell carcinoma risk factors, but the following features are established:<ref name="pmid9118025">{{cite journal| author=Saku T, Hayashi Y, Takahara O, Matsuura H, Tokunaga M, Tokunaga M et al.| title=Salivary gland tumors among atomic bomb survivors, 1950-1987. | journal=Cancer | year= 1997 | volume= 79 | issue= 8 | pages= 1465-75 | pmid=9118025 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9118025  }}</ref><ref name="pmid10539921">{{cite journal| author=Depowski PL, Setzen G, Chui A, Koltai PJ, Dollar J, Ross JS| title=Familial occurrence of acinic cell carcinoma of the parotid gland. | journal=Arch Pathol Lab Med | year= 1999 | volume= 123 | issue= 11 | pages= 1118-20 | pmid=10539921 | doi=10.1043/0003-9985(1999)123<1118:FOOACC>2.0.CO;2 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10539921  }}</ref><ref name="VilleneuveTremblay2011">{{cite journal|last1=Villeneuve|first1=Hugo|last2=Tremblay|first2=Steve|last3=Galiatsatos|first3=Polymnia|last4=Hamel|first4=Nancy|last5=Guertin|first5=Louis|last6=Morency|first6=Renald|last7=Tischkowitz|first7=Marc|title=Acinic cell carcinoma of the retromolar trigone region: expanding the tumor phenotype in Cowden syndrome?|journal=Familial Cancer|volume=10|issue=4|year=2011|pages=691–694|issn=1389-9600|doi=10.1007/s10689-011-9472-8}}</ref>
 
* Familial predisposition
* Previous radiation exposure
* there were no cases among long-term atomic bomb survivors
* [[Cowden syndrome]]  
* Acinic breast cancer may develop in a [[BRCA1]] mutation carrier


==References==
==References==

Latest revision as of 03:43, 9 October 2019

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ramyar Ghandriz MD[2]

Overview

There is very little approved information about acinic cell carcinoma risk factors but Familial predisposition Previous radiation exposure may play an important role.

Risk Factors

Common risk factors in the development of acinic cell carcinoma include:

Common Risk Factors

  • Common risk factors in the development of acinic cell carcinoma may be occupational, environmental, genetic[1][2][3].
  • Common risk factors in the development of acinic cell carcinoma include:
    • Familial predisposition
    • Previous radiation exposure
    • Cowden syndrome
    • Acinic breast cancer may develop in a BRCA1 mutation carrier
    • There were no cases among long-term atomic bomb survivors

References

  1. Saku T, Hayashi Y, Takahara O, Matsuura H, Tokunaga M, Tokunaga M; et al. (1997). "Salivary gland tumors among atomic bomb survivors, 1950-1987". Cancer. 79 (8): 1465–75. PMID 9118025.
  2. Depowski PL, Setzen G, Chui A, Koltai PJ, Dollar J, Ross JS (1999). "Familial occurrence of acinic cell carcinoma of the parotid gland". Arch Pathol Lab Med. 123 (11): 1118–20. doi:10.1043/0003-9985(1999)123<1118:FOOACC>2.0.CO;2. PMID 10539921.
  3. Villeneuve, Hugo; Tremblay, Steve; Galiatsatos, Polymnia; Hamel, Nancy; Guertin, Louis; Morency, Renald; Tischkowitz, Marc (2011). "Acinic cell carcinoma of the retromolar trigone region: expanding the tumor phenotype in Cowden syndrome?". Familial Cancer. 10 (4): 691–694. doi:10.1007/s10689-011-9472-8. ISSN 1389-9600.

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