Lynch sendromunda profilaktik cerrahi: Ne zaman ve nasıl?– Güncel yaklaşımlar ve literatür derlemesi
Öz
Anahtar Kelimeler
Kaynakça
- 1. Boland CR, Lynch HT. The history of Lynch syndrome. Fam Cancer. 2013;12(2):145-57. Doi: 10.1007/s10689-013-9637-8.
- 2. Groden J, Thliveris A, Samowitz W, Carlson M, Gelbert L, Albertsen H, et al. Identification and characterization of the familial adenomatous polyposis coli gene. Cell. 1991;66(3):589–600. doi: 10.1016/0092-8674(81)90021-0.
- 3. Lynch HT, Snyder CL, Shaw TG, Heinen CD, Hitchins MP. Milestones of Lynch syndrome: 1895-2015. Nat Rev Cancer. 2015;15(3):181-94. doi: 10.1038/nrc3878.
- 4. Jass J, Stewart S, Stewart J, Lane MR. Hereditary non-polyposis colorectal cancer--morphologies, genes and mutations. Mutat Res. 1994;310(1):125–33. doi: 10.1016/0027-5107(94)90016-7.
- 5. Lynch HT, de la Chapelle A. Hereditary colorectal cancer. N Engl J Med. 2003;348(10):919-32. doi: 10.1056/NEJMra012242.
- 6. Win AK, Young JP, Lindor NM, Tucker MK, Ahnen DJ, Young GP,et al. Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort study. J Clin Oncol 2012;30(9):958-64. doi: 10.1200/JCO.2011.39.5590.
- 7. Guillem JG, Smith AJ, Calle JP, Ruo L. Gastrointestinal polyposis syndromes. Curr Probl Surg. 1999;36(4):217-323. doi: 10.1016/s0011-3840(99)80013-6.
- 8. Goodenberger ML, Thomas BC, Riegert-Johnson D, Boland CR, Plon SE, Clendenning M, et al. PMS2 monoallelic mutation carriers: the known unknown. Genet Med. 2016;18(1):13-9. doi: 10.1038/gim.2015.27
Ayrıntılar
Birincil Dil
Türkçe
Konular
Cerrahi
Bölüm
Derleme
Yazarlar
Emrah Akın
*
0000-0003-0224-3834
Türkiye
Uğur Can Dülger
0000-0001-5476-715X
Türkiye
Fatih Altıntoprak
0000-0002-3939-8293
Türkiye
Yayımlanma Tarihi
30 Nisan 2021
Gönderilme Tarihi
23 Ocak 2021
Kabul Tarihi
5 Mart 2021
Yayımlandığı Sayı
Yıl 2021 Cilt: 4 Sayı: 1