Rectal cancer in hereditary nonpolyposis colorectal cancer

被引:36
|
作者
Lee, JS
Petrelli, NJ
Rodriguez-Bigas, MA
机构
[1] Roswell Pk Canc Inst, Dept Surg, Buffalo, NY 14263 USA
[2] SUNY Buffalo, Buffalo, NY 14263 USA
来源
AMERICAN JOURNAL OF SURGERY | 2001年 / 181卷 / 03期
关键词
rectal cancer; colorectal cancer; hereditary nonpolyposis colorectal cancer; HNPCC; hereditary cancer syndromes;
D O I
10.1016/S0002-9610(01)00568-2
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Hereditary nonpolyposis colorectal cancer (HNPCC) accounts for approximately 2% to 5% of all colorectal cancers. Rectal cancer in HNPCC is not well characterized. Methods: A retrospective medical record review of HNPCC patients with colorectal cancer diagnosis from December 1948 to December 1999 was performed in an attempt to elucidate the natural history of rectal cancer in HNPCC. Group A consisted of patients diagnosed with rectal cancer as the index colorectal cancer. Group B consisted of patients diagnosed with rectal cancer as a metachronous colorectal cancer. Results: Twenty-five of 104 patients developed rectal cancer in our HNPCC registry. There were 18 patients in group A with a median age at diagnosis of rectal cancer of 48 years (range 24 to 79) and 7 patients in group B diagnosed at a median age of 58 years (range 45 to 68). Three of 18 patients (17%) in group A developed metachronous colon cancers at a median of 203 months (range 27 to 373) from the index rectal cancer. Rectal cancer in group B was diagnosed at a median 245 months (range 51 to 564) from the index colorectal cancer diagnosis. Conclusions: Rectal cancer in HNPCC is not uncommon. The presentation of rectal carcinoma should not obviate the evaluation for HNPCC in suspected cases. (C) 2001 Excerpta Medica, Inc. All rights reserved.
引用
收藏
页码:207 / 210
页数:4
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