ABSTRACT
Colorectal cancer is one of the major causes of cancer deaths in both men and women.
It is estimated that ∼5% to 10% of patients with colorectal cancer have an inherited
germline mutation that predisposes them to cancer. Clinically, hereditary colorectal
cancer syndromes can be divided into those associated with colonic polyposis (familial
adenomatous polyposis, attenuated familial adenomatous polyposis, and MYH-associated polyposis) and those not associated with colonic polyposis (hereditary
nonpolyposis colon cancer).
Treatment options for these patients include multiple aggressive screening regimens,
chemopreventive medications, and prophylactic surgery. Selection of the appropriate
management approach is best made using information obtained from the patient's clinical
examination, the family medical history, and genetic evaluation. Compliance is improved
when patients completely understand their disease and participate fully in the formulation
of the treatment plan. Although not proved, it seems reasonable that this approach
may prevent the poor outcomes so frequently associated with inherited cancer syndromes.
KEYWORDS
Familial adenomatous polyposis - attenuated familial polyposis -
MYH-associated polyposis - hereditary nonpolyposis colon cancer
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C. Neal EllisM.D.
Department of Surgery, University of South Alabama
2451 Fillingim St., 706 Mastin Bldg.
Mobile, AL 36617-2293
Email: nellis@usouthal.edu