de Jong Andrea E, Morreau Hans, Nagengast Fokko M, Mathus-Vliegen Elisabeth M H, Kleibeuker Jan H, Griffioen Gerrit, Cats Annemieke, Vasen Hans F A
The Netherlands Foundation for the Detection of Hereditary Tumours, Leiden University medical Center, Poortgebouw Zuid, 2333 AA Leiden, The Netherlands.
Am J Gastroenterol. 2005 Jan;100(1):139-43. doi: 10.1111/j.1572-0241.2005.41000.x.
We evaluated the prevalence and characteristics of adenomas in a young population not genetically predisposed for the development of colorectal cancer (CRC).
The databases of the Dutch Hereditary Colorectal Cancer Registry were used. The study population included patients (n = 444) who had regular endoscopy until mutation analysis revealed they did not carry the (Adenomatous Polyposis Coli (APC)/Mismatch Repair) gene defect identified in their family.
At first colonoscopy (n = 342; 50% males, mean age 37 yr) a total of 19 adenomas (10 males, mean age 50 yr, range 24-91 yr) and two CRCs (2 males, age 49 and 72 yr) were identified, and at first sigmoidoscopy (n = 102; 53% males, mean age 29 yr) three adenomas (2 males, age 8, 40, and 41 yr) were found. A second colonoscopy was performed in 14 patients with, and in 162 patients without an adenoma. Three of 14 patients (21%) developed a new adenoma (all >50 yr) and 8 of 162 (5%) patients developed their first adenoma during follow-up. In the colonoscopy group, the cumulative proportion of patients free of adenomas at age 50 yr was 86%. Of all adenomas diagnosed during colonoscopy (n = 49), 65% were located distal from the flexura lienalis. Of the adenomas detected during all endoscopies (n = 53), 9.8% were > or =7 mm, 7.5% showed high-grade dysplasia, and 7.5% showed tubulovillous features.
On the basis of our findings during colonoscopy we conclude that the risk of developing adenomas/CRC in young individuals without genetic risk factors is low. Adenoma surveillance programs should focus on young individuals with a positive family (or personal) history for adenomas/CRC, or on individuals >50 yr.
我们评估了在非遗传性结直肠癌(CRC)发病风险的年轻人群中腺瘤的患病率及特征。
使用荷兰遗传性结直肠癌登记数据库。研究人群包括接受常规内镜检查的患者(n = 444),直至突变分析显示他们未携带在其家族中鉴定出的(腺瘤性息肉病 coli(APC)/错配修复)基因缺陷。
在首次结肠镜检查时(n = 342;50%为男性,平均年龄37岁),共发现19个腺瘤(10名男性,平均年龄50岁,范围24 - 91岁)和2例CRC(2名男性,年龄49岁和72岁),在首次乙状结肠镜检查时(n = 102;53%为男性,平均年龄29岁)发现3个腺瘤(2名男性,年龄8岁、40岁和41岁)。14例有腺瘤和162例无腺瘤的患者接受了第二次结肠镜检查。14例患者中有3例(21%)出现新的腺瘤(均>50岁),162例患者中有8例(5%)在随访期间出现首个腺瘤。在结肠镜检查组中,50岁时无腺瘤患者的累积比例为86%。在结肠镜检查期间诊断出的所有腺瘤(n = 49)中,65%位于脾曲远端。在所有内镜检查中检测到的腺瘤(n = 53)中,9.8%直径≥7 mm,7.5%显示高级别发育异常,7.5%显示绒毛管状特征。
基于我们在结肠镜检查中的发现,我们得出结论,在无遗传风险因素的年轻个体中发生腺瘤/CRC的风险较低。腺瘤监测计划应侧重于有腺瘤/CRC家族(或个人)史阳性的年轻个体,或年龄>50岁的个体。