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Surgical management of hereditary colorectal cancer: surgery based on molecular analysis and family history
被引:0
|作者:
Perea, J.
[1
]
Justo, I.
[1
]
Alvaro, E.
[1
]
Lomas, M.
[1
]
Diaz Tasende, J.
[2
]
Marin, J. C.
[2
]
Franco, A.
[2
]
Colina, F.
[3
,4
]
Rodriguez, Y.
[3
]
Martinez, J.
[5
]
Robles, L.
[6
]
Urioste, M.
[7
]
Hidalgo, M.
[1
]
机构:
[1] 12 Octubre Univ Hosp, Dept Gen Surg B, Madrid, Spain
[2] 12 Octubre Univ Hosp, Dept Gastroenterol, Madrid, Spain
[3] 12 Octubre Univ Hosp, Dept Pathol, Madrid, Spain
[4] 12 Octubre Univ Hosp, Dept Tumor Registry, Madrid, Spain
[5] 12 Octubre Univ Hosp, Mol Biol Unit, Madrid, Spain
[6] 12 Octubre Univ Hosp, Genet Counsel Unit, Dept Oncol, Madrid, Spain
[7] Spanish Natl Canc Res Ctr, Human Genet Grp, Madrid, Spain
关键词:
Colorectal cancer;
Surgery;
Lynch syndrome;
Familial adenomatous polyposis;
Familial colorectal cancer type X;
ADENOMATOUS POLYPOSIS;
LYNCH-SYNDROME;
SURVEILLANCE;
POPULATION;
CRITERIA;
D O I:
暂无
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
摘要:
The importance of colorectal cancer (CRC) is increasing. A proportion show a hereditary component, as in Lynch syndrome and Familial Adenomatous Polyposis, and a recently defined entity as well, namely, Familial Colorectal Cancer type X. The high probability to develop CRC in these groups may, at the time of recognition, change surgical management, including its timing or even the surgical technique. In some cases prophylactic surgery can play an important role. The possibility of using tools that allow recognition of the aforementioned syndromes, including microsatellite instability, immunohistochemistry for DNA mismatch repair system proteins, and especially their mutations, is on the basis of therapeutic strategies that differ from those employed in sporadic CRC cases.
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页码:536 / 540
页数:5
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