Skip to main content
The Korean Journal of Internal Medicine logoLink to The Korean Journal of Internal Medicine
. 2017 Nov 8;34(1):65–71. doi: 10.3904/kjim.2016.063

Clinicopathological features of colorectal polyps in 2002 and 2012

Yoon Jeong Nam 1, Kyeong Ok Kim 1,, Chan Seo Park 1, Si Hyung Lee 1, Byung Ik Jang 1
PMCID: PMC6325443  PMID: 29108402

Abstract

Background/Aims

There are few comparative studies on the historical changes in the clinicopathologic characteristics of colorectal polyps in Korea. This retrospective study compared the clinicopathologic characteristics of colorectal polyps treated at our institution in 2002 and 2012.

Methods

The medical records of 1,816 patients who underwent colonoscopy and were found to have colorectal polyps in 2002 (n = 597) or 2012 (n = 1,219) were reviewed retrospectively. Patient characteristics and polyp sizes, gross morphologies, locations, and pathologic results were analyzed and compared.

Results

Mean age was older in the 2002 group than in the 2012 group (67.3 ± 11.1 years vs. 55.4 ± 10.8 years, p < 0.001). The 1,816 study subjects had a total of 3,723 colorectal polyps, with a mean of 2.05 polyps per patient. Mean polyp size was larger in the 2002 group than in the 2012 group (0.6 ± 0.4 cm vs. 0.4 ± 0.3 cm, p < 0.001). The most common histology was tubular adenoma and they were more common in the right colon in both study groups. Although the distribution of total adenoma was not significantly different between groups, the location of advanced adenoma differed significantly and was more common in the right colon in the 2012 group (30.4% vs. 63.2%, p = 0.01).

Conclusions

No significant change in total polyps and adenoma distribution was found between 2002 and 2012. However, advanced adenoma was more common in the right colon in 2012, which cautiously suggests a locational shift from the left to right colon. These findings indicate that right colon polyps require more attention.

Keywords: Colonic polyps, Distribution, Adenoma

INTRODUCTION

Eighty percent of colorectal cancers (CRCs) arise from preexisting adenomas [1], and the localization and anatomical distribution of adenomatous polyps are viewed with increasing importance. In the era of screening colonoscopy, the colorectal polyp detection rate is increasing. Colonoscopy continues to be considered as the gold standard screening tool for colon cancer prevention because it enables the removal of precancerous adenomas [2].

An estimated 30% of the Western population has colon polyps, but a lower rate (10% to 15%) is reported for Asians and Africans [3,4]. In a recent Korean study on colonoscopy results obtained after health examinations, it was found that more than half of examinees older than 50 and one-thirds of young examinees, including individuals in their 30s and 40s, had colon polyps [5]. Previous studies have shown that colon polyps are more common in men than in women and that prevalence increases with age [6,7].

A locational shift of colorectal adenomas and carcinomas toward the right colon has been observed in the United States and Europe [8,9], and time trend analysis has shown a progressive shift toward right-sided colon cancer in the past 40 years [10].

An understanding of the chronological changes in colorectal polyps and cancer is very important because these are associated with the efficacy of colorectal screening strategies. However, few chronological comparative studies have been conducted on colorectal polyps. In the present study, we compared the clinicopathological features of colorectal polyps recorded in 2002 with those documented in 2012, with focus on anatomical distribution.

METHODS

This was a retrospective observational study comparing clinicopathological differences over a 10-year period. Initially, the medical records of 4,791 patients who underwent colonoscopy at Yeungnam University Hospital in 2002 (n = 1,562) and 2012 (n = 3,229) were reviewed retrospectively. Patients were excluded if they had (1) a history of CRC, (2) a history of colectomy, (3) regular colonoscopy for previously diagnosed colorectal polyps, (4) inflammatory bowel disease, (5) hereditary polyposis syndrome, or (6) diagnosis of advanced CRC. However, patients with a confirmed intramucosal carcinoma after endoscopic or surgical resection were all included.

Of these 4,791 patients, 784 were excluded; of the remaining 4,007, 1,816 were found to have polyps (n = 3,723). These 1,816 patients constituted the study cohort and were allocated to a 2002 group (n = 597) or a 2012 group (n = 1,219) (Fig. 1).

Figure 1.

Figure 1.

Study flow chart of enrolled patients.

All polyps found during colonoscopy were removed using a biopsy forceps or by snare polypectomy, endoscopic resection and endoscopic submucosal dissection or surgery and were referred for histological examination.

The 2002 and 2012 groups were compared with respect to patient characteristics and polyp sizes, gross morphologies, distributions, and histologies. Polyp locations were classified into eight categories—cecum, ascending colon, hepatic flexure, transverse colon, splenic flexure, descending colon, sigmoid colon, and rectum—and then further classified as right- or left-side colon origin. Right-sided polyps were defined as any polyps detected between the splenic flexure and cecum, and left-sided polyps as polyps located distal to the splenic flexure. Polyp sizes were classified as follows: diminutive (< 5 mm in diameter), small (≥ 5 mm to < 10 mm), and large (≥ 10 mm). Gross morphologies were described as pedunculated (Ip), subpedunculated (Isp), sessile (Is), or flat (IIa), according to the Paris classification [11].

Histology was classified as neoplastic polyp including tubular adenoma, tubulovillous adenoma, villous adenoma, serrated adenoma, adenocarcinoma, or non-neoplastic polyp including hyperplastic polyp and inflammation. Cases of not able to be defined as neoplastic or non- neoplastic were all classified into others. Advanced adenoma was defined as villous or tubulovillous adenoma, high-grade dysplasia, intramucosal carcinoma, or as an adenoma of diameter ≥ 10 mm.

Statistical analysis was carried out using SPSS version 15.0 (SPSS Inc., Chicago, IL, USA). Results are expressed as means and standard deviations for continuous variables or as percentages for categorical variables. Differences in clinical characteristics for different segments were analyzed using the chi-square test for categorical variables and by analysis of variance for quantitative variables. Statistical significance was accepted for p values < 0.05.

This study was approved by the Institutional Review Board of Yeungnam University Hospital (YUH-13-0390-O38). Written informed consent by the patients was waived due to a retrospective nature of our study.

RESULTS

Baseline characteristics and clinicopathological characteristics of polyps

Among the 4,007 patients who met the inclusion criteria, 1,816 patients with polyps at colonoscopy were included in the analysis. The male to female ratio for all 1,816 study subjects was 1.5:1, and the male to female ratio in the 2012 group was significantly higher than in the 2002 group (1.8:1 vs. 2.3:1, p = 0.038). On the other hand, mean age in the 2002 group was significantly higher than in the 2012 group (67.3 ± 11.1 vs. 55.4 ± 10.8, p < 0.001).

The annual number of colonoscopic examinations performed doubled over the study period. When we consider the indications, 592 individuals (48.6%) underwent colonoscopy during health examinations in 2012, but in 2002, most colonoscopies were performed because of symptoms or medical indications.

Polyp detection rate in 2002 was 45.5% and 45.2% in 2012 (p = 0.091). The mean number of polyps per patient was not different between groups (2.2 ± 1.7 vs. 2.0 ± 1.5, p = 0.056). Adenoma was detected in 31.3% of the 4,007 patients; the adenoma detection rate did not show a significant difference between 2002 and 2012 (31.1% vs. 31.5%, p = 0.064) (Table 1).

Table 1.

Baseline characteristics of patients with colorectal polyp(s)

Variable 2002 Group 2012 Group p value
Sex, male:female 1.8:1 2.3:1 0.038
Age, yr 67.3 ± 11.1 55.4 ± 10.8 < 0.001
Indication 0.025
 Screening/survaillancea 221 (32.0) 592 (48.6)
 Abdominal pain 132 (27.1) 171 (14.0)
 Melena/hematochezia 163 (27.3) 204 (16.7)
 Othersb 81 (13.6) 252 (20.7)
Polyp detection ratec 597/1,312 (45.5) 1,219/2,695 (45.2) 0.091
Polyps per patients 2.2 ± 1.7 2.0 ± 1.5 0.056
Adenoma detection rated 408/1,312 (31.1) 849/2,695 (31.5) 0.064
Right:left:both 187 (31.3):242 (40.5):168 (28.2) 391 (32.1):491 (40.3):337 (27.6) 0.945

Values are presented as mean ± standard deviation or number (%).

a

Only surveillance and follow-up after negative index colonoscopy were included.

b

Others included diarrhea and anemia.

c

Polyp detection rate was calculated from the number of patients with polyps divided by the total of included patients.

d

Adenoma detection rate was calculated from the number of patients with adenomatous polyps divided by the total of included patients

Polyps were more frequent in the left colon in both groups and there was no significant difference (Table 2). When we analyzed the distribution with only neoplastic polyps, they were both more common in right side colon (435/825 in 2002 vs. 767/1,379 in 2012, p = 0.180).

Table 2.

Clinicopathologic characteristics of 3,723 polyps

Variable 2002 Group (n = 1,277) 2012 Group (n = 2,446) p value
Location 0.012
 Cecum 80 (6.2) 90 (3.7)
 Ascending colon 259 (20.3) 544 (22.2)
 Hepatic flexure 57 (4.5) 98 (4.0)
 Transverse colon 217 (17.0) 387 (15.8)
 Splenic flexure 13 (1.0) 21 (0.9)
 Descending colon 138 (10.8) 287 (11.7)
 Sigmoid colon 291 (22.8) 611 (25.0)
 Rectum 222 (17.4) 408 (16.7)
Right:left 626 (49.0):651 (51.0) 1,140 (46.6):1,306 (53.4) 0.767
Shape < 0.001
 Pedunculated 64 (5.0) 28 (1.1)
 Subpedunculated 87 (6.8) 395 (16.1)
 Sessile 552 (43.2) 1,433 (58.6)
 Flat 574 (45.0) 590 (24.2)
Size, mma 0.6 ± 0.4 0.4 ± 0.3 < 0.001
 Diminutive 613 (48.0) 1,790 (73.2)
 Small 429 (33.6) 541 (22.1)
 Large 235 (18.4) 115 (4.7)
Histology < 0.001
 Neoplastic polyp
  Tubular adenoma 786 (61.6) 1,334 (54.5)
  Tubulovillous 21 (1.6) 21 (0.9)
  Villous adenoma 4 (0.3) 4 (0.2)
  Serrated adenoma 3 (0.2) 13 (0.5)
  Adenocarcinoma 11 (0.9) 7 (0.3)
 Non-neoplastic polyp 435 (34.1) 1,063 (43.4)
 Othersb 17 (1.3) 4 (0.2)

Values are presented as number (%) or mean ± standard deviation.

a

Diminutive, < 5 mm; small, ≥ 5 to < 10 mm; large, ≥ 10 mm.

b

Adenomatous change, 15; atypical gland, 2; eosinophilic infiltration, 1; fat necrosis, 2; xanthoma, 1.

The flat type was the most common morphology in the 2002 group, but in the 2012, sessile type was most common. Mean polyp size was larger in the 2002 group (0.6 ± 0.4 cm vs. 0.4 ± 0.3 cm, p < 0.001) and tubular adenoma was the most common histology (61.6% in 2002 and 54.5% in 2012) (Table 2).

Clinical characteristics of advanced adenoma

Of the 3,723 polyps excised, 113 were diagnosed as advanced adenoma, which was more common in the 2002 group (56, 4.4% vs. 57, 2.3%). There was no significant difference in age of the patients with advanced adenoma (67.8 ± 10.5 years vs. 64.1 ± 12.5 years, p = 0.226).

Rectum was most common location (25.7%), followed by the sigmoid (20.4%) and ascending colon (17.7%). In the 2002 group, 30.4% of advanced adenomas were located in the right colon, whereas in the 2012 group, 63.2% were located in the right colon (p = 0.012). Mean size in the 2012 groups was larger than in 2002 group (1.5 ± 0.8 cm and 2. 1± 1.2 cm, respectively) (Table 3).

Table 3.

Histologic and morphologic characteristics of advanced adenomas in the two groups

Variable 2002 Group (n = 1,277) 2012 Group (n = 2,446) p value
Age, yr 67.8 ± 10.5 64.1 ± 12.5 0.226
Location, right:left 17 (30.4):39 (69.6) 36 (63.2):21 (36.8) 0.010
Shape
 Pedunculated 17 (30.4) 5 (8.8)
 Subpedunculated 10 (17.8) 13 (22.8)
 Sessile 17 (30.4) 18 (31.6)
 Flat 12 (21.4) 21 (36.8)
Size, cm 1.5 ± 0.8 2.1 ± 1.2 0.145
Histology 0.104
 Tubular adenoma 13 (23.2) 19 (33.3)
 Villous adenoma 4 (7.1) 4 (7.0)
 Tubulovillous adenoma 12 (21.4) 14 (24.6)
 High grade dysplasia 16 (28.6) 13 (22.8)
 Adenocarcinoma 11 (19.6) 7 (12.3)

Values are presented as mean ± standard deviation or number (%)

Histologically, high-grade dysplasia or intramucosal carcinoma was diagnosed in 47 polyps (27 in 2002 and 20 in 2012). Intramucosal cancer and of high-grade dysplasia in the 2012 group were detected more frequently in the right colon (22.2% vs. 65.0%, p = 0.023) (Table 4).

Table 4.

Locations and sizes of carcinoma in situ including high-grade dysplasia and intramucosal adenocarcinoma in the two groups

Variable 2002 Group (n = 27) 2012 Group (n = 20) p value
Age, yr 66.5 ± 9.8 63.0 ± 12.5 0.404
Location, right:left 6 (22.2):21 (77.8) 13 (65.0):7 (35.0) 0.023
Size, cm 1.9 ± 0.8 2.4 ± 1.4 0.278

Values are presented as mean ± standard deviation or number (%).

DISCUSSION

In Korea, the incidence of CRC has increased and the importance of prevention and screening of CRC has been emphasized [12]. Colnoscopy has been considered one of the most effective screening modalities because detection and remove of the colorectal polyp using colonoscopy can reduce the incidence of CRC by up to 90% [1,13].

Youn et al. [14] reported that the detection rate of polyps had increased from 5.1% in the 1970s to 9.5% in the 1990s. In a recent Western study by Raju et al. [15], the rate of adenoma detection was 60% and the rate of precancerous lesion detection was as high as 66%. In the present study, there was no significant change in the polyp detection rate over this 10-year period.

We also found that mean polyp size was significantly larger in 2002 than in 2012. This result presumably was associated with the increased performances of screening colonoscopy and equipment such as a cap in 2012. On the other hand, the sizes of intramucosal cancer and high-grade dysplasia among cases of advanced adenoma were about 5 mm larger in 2012. These differences in sizes reflect the recent increase in the endoscopic treatment of larger, advanced polyps, especially with endoscopic mucosal resection or submucosal dissection.

In our study, the prevalence of advanced adenoma was higher in 2002 than in 2012. However, it might be associated with the differences in indications and patients’ age. Actually in 2002, patients underwent colonoscopy when they had symptoms; in 2012, screening or surveillance after negative index colonoscopy was most common. Older age predominated in 2002, also affecting the prevalence of advanced adenoma. Thus, we could not conclude that advanced adenomas decreased in 2012 compared with in 2002.

The incidence of right-sided colon cancer has been increasing in Korea and its clinical importance has been emphasized [16]. A recent study showed that the developmental pathways of left- and right-sided colon cancer and their responses to chemotherapy differs [17,18]. In addition, it has been suggested that the distribution of colon polyps started to shift from the left to right colon 10 years ago [13,19,20]. Our study also showed that neoplastic polyps were more common in right side colon in both groups; thus, it appears that the shift of adenoma to right colon began from 10 years ago in our study.

Interestingly, the distribution of advanced adenoma was different between groups. The possible causes are that we could not rule out the possibility of missed lesions at negative index colonoscopy although we excluded patients with a history of colon polyps at previous colonoscopy. Secondly, we cautiously suggested that our result could reflect the current polyp trend. Actually, several previous Western and Oriental studies reported a left to right shift of colorectal polyp and cancer [8-10].

The present study has several limitations. First, it is limited by its retrospective, single-center design. We could not identify risk factors such as smoking, family history, and body mass index completely. In that reasons, we could not represent the colorectal polyp trend in Korea. Second, the 2012 group contained more asymptomatic examinees and fewer older examinees with medical conditions than the 2002 group. The use of screening endoscopy continues to increase, mean patient age has fallen, and the small polyp detection rate is increasing. We tried to reduce selection bias by adopting strict criteria, and excluded patients who underwent follow-up colonoscopy after polypectomy. However, there were significant differences in age and gender, and these differences could have affected the results. However, we found no significant differences in the prevalence of polyps and total adenomas. Additionally, these results might suggest the possibility of an increase in other risk factors such as westernized diets and obesity in Korea. Nevertheless, the present study was conducted with a relatively large number of patients and shows a difference in distribution of advanced adenoma (left colon < right) between 2002 and 2012.

In conclusion, we found no significant difference in polyp prevalence and distribution between 2002 and 2012; however, advanced adenoma was more common in the right colon in 2012. Although a prospective, long-term study with a large number of patients is needed for confirmation, our results suggest that additional effort should be directed at detection and more active treatment of right-sided colon polyps.

KEY MESSAGE

1. Overally, there was no significant difference in polyp prevalence and distribution between 2002 and 2012.

2. Compared to 10 years ago, advanced adenoma was more common in right side colon and we need more attention when we exam right side colon.

Acknowledgments

This study was supported by 2015 Yeungnam University Research Grant.

Footnotes

No potential conflict of interest relevant to this article was reported.

REFERENCES

  • 1.Nouraie M, Hosseinkhah F, Brim H, Zamanifekri B, Smoot DT, Ashktorab H. Clinicopathological features of colon polyps from African-Americans. Dig Dis Sci. 2010;55:1442–1449. doi: 10.1007/s10620-010-1133-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Visovan II, Tantau M, Ciobanu L, Pascu O, Tantau A. Increasing prevalence of right-sided colonic adenomas in a high-volume endoscopy department in Romania: implications for colorectal cancer screening. J Gastrointestin Liver Dis. 2014;23:147–151. doi: 10.15403/jgld.2014.1121.232.iiv1. [DOI] [PubMed] [Google Scholar]
  • 3.Coode PE, Chan KW, Chan YT. Polyps and diverticula of the large intestine: a necropsy survey in Hong Kong. Gut. 1985;26:1045–1048. doi: 10.1136/gut.26.10.1045. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Tony J, Harish K, Ramachandran TM, Sunilkumar K, Thomas V. Profile of colonic polyps in a southern Indian population. Indian J Gastroenterol. 2007;26:127–129. [PubMed] [Google Scholar]
  • 5.Jung KW, Park S, Kong HJ, et al. Cancer statistics in Korea: incidence, mortality, survival, and prevalence in 2009. Cancer Res Treat. 2012;44:11–24. doi: 10.4143/crt.2012.44.1.11. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Weston AP, Campbell DR. Diminutive colonic polyps: histopathology, spatial distribution, concomitant significant lesions, and treatment complications. Am J Gastroenterol. 1995;90:24–28. [PubMed] [Google Scholar]
  • 7.Villavicencio RT, Rex DK. Colonic adenomas: prevalence and incidence rates, growth rates, and miss rates at colonoscopy. Semin Gastrointest Dis. 2000;11:185–193. [PubMed] [Google Scholar]
  • 8.Greene FL. Distribution of colorectal neoplasms: a left to right shift of polyps and cancer. Am Surg. 1983;49:62–65. [PubMed] [Google Scholar]
  • 9.Chan AO, Hui WM, Chan CK, et al. Colonoscopy demand and practice in a regional hospital over 9 years in Hong Kong: resource implication for cancer screening. Digestion. 2006;73:84–88. doi: 10.1159/000094038. [DOI] [PubMed] [Google Scholar]
  • 10.Thorn M, Bergstrom R, Kressner U, Sparen P, Zack M, Ekbom A. Trends in colorectal cancer incidence in Sweden 1959-93 by gender, localization, time period, and birth cohort. Cancer Causes Control. 1998;9:145–152. doi: 10.1023/a:1008826109697. [DOI] [PubMed] [Google Scholar]
  • 11.van Doorn SC, Hazewinkel Y, East JE, et al. Polyp morphology: an interobserver evaluation for the Paris classification among international experts. Am J Gastroenterol. 2015;110:180–187. doi: 10.1038/ajg.2014.326. [DOI] [PubMed] [Google Scholar]
  • 12.Cheng L, Eng C, Nieman LZ, Kapadia AS, Du XL. Trends in colorectal cancer incidence by anatomic site and disease stage in the United States from 1976 to 2005. Am J Clin Oncol. 2011;34:573–580. doi: 10.1097/COC.0b013e3181fe41ed. [DOI] [PubMed] [Google Scholar]
  • 13.Siegel RL, Ward EM, Jemal A. Trends in colorectal cancer incidence rates in the United States by tumor location and stage, 1992-2008. Cancer Epidemiol Biomarkers Prev. 2012;21:411–416. doi: 10.1158/1055-9965.EPI-11-1020. [DOI] [PubMed] [Google Scholar]
  • 14.Youn SJ, Kim NY, Kim YT, et al. Colorectal polyp in Korea. Korean J Gastroenterol. 1991;23:450–458. [Google Scholar]
  • 15.Raju GS, Vadyala V, Slack R, et al. Adenoma detection in patients undergoing a comprehensive colonoscopy screening. Cancer Med. 2013;2:391–402. doi: 10.1002/cam4.73. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Um WH, Kim HG, Jeon SR, et al. Clinical comparison for colon polyps between right and left colon in Koreans. Intest Res. 2012;10:372–378. [Google Scholar]
  • 17.Bufill JA. Colorectal cancer: evidence for distinct genetic categories based on proximal or distal tumor location. Ann Intern Med. 1990;113:779–788. doi: 10.7326/0003-4819-113-10-779. [DOI] [PubMed] [Google Scholar]
  • 18.Delattre O, Olschwang S, Law DJ, et al. Multiple genetic alterations in distal and proximal colorectal cancer. Lancet. 1989;2:353–356. doi: 10.1016/s0140-6736(89)90537-0. [DOI] [PubMed] [Google Scholar]
  • 19.Okamoto M, Kawabe T, Yamaji Y, et al. Flat-type early colorectal cancer preferentially develops in right-sided colon in older patients. Dis Colon Rectum. 2005;48:101–107. doi: 10.1007/s10350-004-0754-1. [DOI] [PubMed] [Google Scholar]
  • 20.Lucendo AJ, Guagnozzi D, Angueira T, et al. The relationship between proximal and distal colonic adenomas: is screening sigmoidoscopy enough in the presence of a changing epidemiology? Eur J Gastroenterol Hepatol. 2013;25:973–980. doi: 10.1097/MEG.0b013e3283614b57. [DOI] [PubMed] [Google Scholar]

Articles from The Korean Journal of Internal Medicine are provided here courtesy of Korean Association of Internal Medicine

RESOURCES