|Year : 2005 | Volume
| Issue : 4 | Page : 204-207
The indirect role of site distribution in high-grade dysplasia in adenomatous colorectal polyps
N Khatibzadeh1, SA Ziaee1, N Rahbar2, S Molanie3, L Arefian3, SA Fanaie2
1 Azad–Tehran University of Medical Science, Tehran, Iran
2 Department of Surgery, Milad Hospital, Tehran, Iran
3 Department of Pathology, Milad Hospital, Tehran, Iran
S A Ziaee
Azad–Tehran University of Medical Science, Tehran
Source of Support: None, Conflict of Interest: None
Background: The appropriate application of Endoscopic modalities for polypectomy depends on the likelihood that the adenoma in question harbors invasive cancer. While prior studies have evaluated polyp size and morphology in assessing the risk of malignancy, in recent decay some authorities have paid more attention to dysplasia. All in all, the relative risk of cancer based on polyp distribution in correlation with dysplasia has not been statistically studied which is done in our study.
Methods and Materials: Between June 2001 and March 2004, the distribution of 130 adenomatous polyps was compared with synchronous invasive or in situ cancer. Factors such as Patient age, Patients gender, location of lesion, size of polyp, histological subtype of adenoma on biopsy, degree of dysplasia, synchronous cancer, color of polyp, and number of polyps were included in the data collection.
Results: Multivariate logistic regression test was used to evaluate the association between malignancy and various clinical variables. It revealed histological subtype, high grade of dysplasia and size to be independent predictor of malignancy. However; left-sided location and histological subtype to be independent risk factor for high-grade dysplasia.
Conclusion: Lesions greater than 1 cm in diameter with high-grade dysplasia after speleinc flexure should be managed as presumptive malignancies with segmental colon resection. In intermediate-risk lesions the physician should decide individually.
Keywords: Adenomatous Polyp, Dysplasia, Colorectal Distribution
|How to cite this article:|
Khatibzadeh N, Ziaee S A, Rahbar N, Molanie S, Arefian L, Fanaie S A. The indirect role of site distribution in high-grade dysplasia in adenomatous colorectal polyps. J Can Res Ther 2005;1:204-7
|How to cite this URL:|
Khatibzadeh N, Ziaee S A, Rahbar N, Molanie S, Arefian L, Fanaie S A. The indirect role of site distribution in high-grade dysplasia in adenomatous colorectal polyps. J Can Res Ther [serial online] 2005 [cited 2016 Aug 28];1:204-7. Available from: http://www.cancerjournal.net/text.asp?2005/1/4/204/19587
| > Introduction|| |
Colorectal Cancer is the most important malignancies in Iran and the second most common cancer overall.Most colorectal cancers are believed to arise from benign adenomatous polyps,,and this concept regarding the adenoma-carcinoma sequence is the main reason for the preventing screening and removal of the adenomatous polyps using colonoscopy. To this end, a great number of studies have focused on endoscopically or surgically removed adenomas, correlating different epidemiologic and pathologic features of the patient and the adenoma respectively with the finding of invasive cancer or future risk.The two factors that have been repeatedly shown to be independent risk factors for malignancy include the size of the lesion and its histologic subtype of adenoma,with the risk of invasive cancer increasing with large, villous type growth. The aim of this study was thus to determine whether the distribution of adenomatous polyps with that of colorectal cancer. We therefore have examined the extent correlation between high-grade dysplasia on biopsies and their distribution has not been studied.
| > Materials and Methods|| |
From approximately 23329 biopsies performed at Milad Hospital Tehran, from Jun 2001 to March 2004, 156 consecutive patients who had undergone biopsy of a solitary adenoma or synchronous invasive or in situ colorectal carcinoma were reviewed. Patients were excluded from analysis if they had been previously diagnosed with familial adenomatous Polyposis or inflammatory bowel disease, or if correlation of the lesions on endoscopy and surgical resection could not be confirmed. All in all, 130 patients were included in our study.Factors such as patient age, patient gender, location of lesion, size of lesion, histologic subtype of adenoma on biopsy, degree of dysplasia on biopsy and resection, synchronous cancer, color of polyp and number of polyps were included in the data collection. Polyps were classified as tubular if they had 0% to 25% villous component, tubulovillous lesion if they contained 26% to 75% villous component, and villous lesions if greater than 75% villous component. Dysplasia was divided into high grade or low grade based on the pathologist's interpretation. All pathology specimens received intradepartmental review. Univariate and multivariate logistic regression was used to evaluate the association between malignancy and various clinical variables.Variables included patient age (by decade), location of lesion and its position to speleinc flexure, size of lesion (< 10 mm, >= 10 mm), histologic subtype of adenoma on biopsy (tubular, tubulovillous, villous), and degree of dysplasia (low or high grade).However, color of polyps and clinical indications of colonoscopy were included in our study.
All variables were treated as unordered categorical variables.
| > Results|| |
Twenty-one of 130 patients (16.2%) were found to have adenocarcinoma on pathologic examination of the surgical specimen. The distribution of adenomatous polyps and general characteristics of adenomas and carcinomas presenting with polyps were summarized in [Table - 1]. However, the variety of polyps' color and colonoscopic indication were explained in [Table - 2].
In our study, high-grade dysplasia, villous histology, left-sided location, and increasing size were all features associated with an increased chance of malignancy. The rate of malignancy rose from 4.1% in biopsies showing low-grade dysplasia to 53.1% in biopsies revealing high-grade dysplasia. Likewise, the histology of the biopsy was predictive of malignancy with tubular, tubulovillous, and villous features corresponding, respectively, to a 2.7%, 22.2% and 44.4% risk of malignancy in the surgical specimen. Size of the lesion revealed an increase in malignancy risk with =< 1 cm and > 1 cm lesions harboring occult malignancy in 10 %, and 36.7% of cases, respectively.
On multivariate analysis, only size, degree of dysplasia, and histologic type of adenoma were independent predictors of a lesion harboring a malignancy. Odd ratios for adenomas grater than 1 cm compared with lesions that were less than 1 cm demonstrated a 3.6-fold increased. High grade of dysplasia on biopsy was associated with an 12.95-fold increased risk of occult cancer compared with low-grade lesions (95% confidence interval= 4.5 to 37.9).However, there was an 16.4-fold increased risk for villous component compared with tubular lesions (95% confidence interval= 4.8 to 83.6).Interestingly, on multivariate analysis, left-sided location and histologic type of adenoma were independent predictors of a lesion harboring a high-grade dysplasia. The shift to left was predictive of dysplasia with before and after speleinc flexure, respectively, to a 5.4%, 32.3%.Segregation of all studies lesions into three risk categories based on the location of adenoma, sized and dysplasia suggests the lowest risk tumors were always benign, whereas the highest risk tumors were almost malignant [Table - 3].
We did not find any significant correlation between color, age, sex and malignancy.
| > Discussion|| |
The presence or absence of invasive cancer is one of the most important determinants of appropriate management of a colonic adenoma.  Size, high-grade dysplasia, and histologic type were all found to be associated with an increased incidence with occult invasive cancer within an adenoma. ,  A number of studies examining large numbers of resected polyps have demonstrated an association between these factors and the incidence of invasive cancer. [Table - 3] We did find there is not the mutual understanding in all studies. The absence of such an association may be due to their selection of risk factors  or the environmental and genetic factors. In Thailand, Rerknimitr showed that right-sided colorectal polyps were more risky than recto sigmoid.  Similarly, however, Yasser H. studied just site distribution between Hispanics and whites.  In our study, high-grade dysplasia on biopsy was a powerful predictor of the presence of invasive cancer in the resected specimens. Similar studies confirmed our conclusion. , , , , , Directly, site distribution had a significant association with dysplasia. It means that left-sided polyps have the potential directly for high grade dysplasia indirectly for invasive or in situ cancer. Also, the role of Site distribution in some studies was mentioned. , , , , , , ,  We believe this association is the first study to examine the ability of high-grade dysplasia and site distribution in an endoscopic biopsy to predict the presence of occult invasive or in situ cancer in adenomas of the colon.
| > Conclusion|| |
Lesions less than 1 cm in diameter without high grade dysplasia located before speleinc flexure can be managed by endoscopic or laparoscopic resection when this expertise is available. Lesions greater than 1 cm in diameter with high-grade dysplasia after speleinc flexure should be managed as presumptive malignancies with segmental colon resection. In the remaining intermediate-risk lesions, treatment decisions will be predicted on the condition of the patient and the physician's treatment philosophy, but can be made with greater precision if the presence or absence of high-grade dysplasia in the biopsy specimen is taken into account.
| > References|| |
|1.||Charles Brunicardi F, Dna K. Anderson, Timothy R. Biliar. Schwartz's Principle of Surgery: Colon,Rectum and Anus, edited by McGrahamHill, New York: Chicago; 2005. p. 1055-119. |
|2.||Tze-Vun Fong, Seng- Kee Chuah, Shue-Shian Chiou. Correlation of the Morphology and Size of Colonic Polyps with Their Distibution. Cang Gung Med J 2003;26:339-43. |
|3.||Wexner S, Cohen S, Ulrich A. Laparoscopic colorectal surgery:are we being honest with our patient? Dis Colon Rectum. 1995;38:723-7. |
|4.||Marvin l. Corman. Colon and Rectum Surgery: Adenoma. 4th edn. 1998. p. 585. |
|5.||Jerome M, McDonald, Tacome, Washington. Pathologic Risk Factors of Occult Malignancy in Endoscopiclly Unresectable Colonic Adenoma. Am J Surg 1999;177:384-7. |
|6.||Lambert R. Early diagnosis and prevention of sporadic colorectal cancer. Endoscopy 2001;33:1042-64. |
|7.||Bj Rembacken. Flat and depressed colonic neoplasams: a prospective study of 1000 colonoscopies in the UK. Lancet 2000;355:1211-4. |
|8.||Nivatvongs S, Nicholson J, Rothenberger D. Villous adenoma of the rectum: the acuaracy of clinical assessment. surgery. 1980:87:549-51. |
|9.||John H. Bond. Polyp Guideline:Diagnosis, Treatment, and Surveillance for Patients With Colorectal Polyps. Am J of Gastoentrology 2000;95:3053-63. |
|10.||Tsai CJ, Lu DK. Small Colorectal Polyps:Histopathology and Clinical Significant. Am J Gastroenterol 1996;91:618-9. |
|11.||Ozick LA, Jacob L, Donelson SS. Distribution of adenomatous polyps in African-Amricans. Am J Gastroenterol 1995;90:758-60. |
|12.||Rerknimitr R, Veskitkul P, Kullavanijaya P. Clinical indication of Patients with Colorectal Neoplasm who underwent colonoscopy at King Chulalongkorn Memorial Hospital presentation of colorectal neoplasm from colonoscopy database). J Med Assos Thai 2003;86:459-64. |
|13.||Yasser H, Shaib, Ehab Rabaa. The site distribution and charactreristic of colorectal adenoma in Hispanic:a comparetive study. Am. J Gastroentro 2002;97:2100. |
|14.||Yamamato M, Mine H, Kusimoto H. Polyps with different grades of dysplasia and their distribution in the colorectum. epatogastroentrology 2004;51:121-3. |
|15.||Gatteschi B, Costantinni M, Bruzzi P. Univariate and Multivariate analyses of the relationship between adenocarcinoma and solitary and multiple adenoma in colorectal adenoma patients. Int J Cancer 1991;49:509-12. |
|16.||Hermanek P, Fruhmorgen P, Guggenmoos Holzmann I. The malignant potential of colorectal polyps;a new statistical approach. Endoscopy 1983;15:16-20. |
|17.||Shinya H, Wolff W. Morphology, anatomic distribution and cancer potential of colonic polyps;an analysis of 7000 polyps endoscopically removed. Am Surg 1970;190:679-83. |
|18.||Betes Ibanez M, Munoz-Navas MA, Duque JM. Diagnostic Value of distal colonic polyps for prediction of advanced proximal neoplasia in an average-risk population undergoing screenin colonoscopy. Gastrintest Endosc 2004;59:634-41. |
|19.||Anderson JC, Alpren Z, Messina CR. Predictors of proximal neoplasia in patients without distal adenomatous pathology. Am J Gastroentrol 2004;99:472-7. |
|20.||Kulling D, Christ AD, Karaaslan N, Fried M. Is histological investigation of polyps always necessary? Endocsopy 2001;33:454-7. |
|21.||Senore C, Segnan N, Bonelli L. Predicting proximal advanced neoplasms at screening sigmoidoscopy. Dis Colon Rectum. 2004;47:1331-40. |
|22.||Pinsky PF, Schoen RE, Weissfeld JL. Predictors of advanced proximal neoplasia in persons with abnormal screening flexible sigmoidoscopy. Clin Gastroenterol Hepatol 2003;1:103-10. |
|23.||Lewis JD, Ng K, Hung KE. Detection of proximal adenomatous polyps with screening sigmoidoscopy:a systemic review and data anaylysis of screenin colonoscopy. Arch Intern Med 2003;163:413-20. |
|24.||Hammer K, Hammer J, Oesterreicher C. Advanced distal colonic lesions as predictors of advanced lesions in proximal colon. Medicine (Baltimore) 2000;79:127-34. |
|25.||R. Scheiden, J. Sand, M. Pandin. Colorectal high-grade adenomas:incidence, localization and adenoma -adenocarcinoma ratio in a retrospective and comparetive population-based study of 225 consequtive cases between 1988 and 1996. Int J of Colorectal Dis 2000;15:29-34. |
|26.||Netzer P, Buttiker U, Pfister M, Halter F, Schmassmann A. Frequency of advanced neoplasia in the proximal colon without an index polyp in the rectosigmoid. Dis Colon Rectum 1999;42:661-7. |
|27.||Yoichi Ikeda, Masaki Mori, Tsukasa Yoshizumi. Cancer and Adenoumatous Polyp Distribution in the Colorectum. Am J Gasteroentol 1999;94:191-3. |
|28.||Grassi A, Casale V, Fracasso P. Medium-large polyps of the colon:a contribution for their clinical profile and a proper surveillance. J Exp Clin Cancer Res 1997;16:313-9. |
|29.||Rocha Ramirez JL, Pena JP., Franco Gutierrez. Colonic Adenoma:risk factors for their malignant transformation.Rev Gastroenterol 1996;61:178-83. |
|30.||Alonso G., Lozzi D, Szram H. Factors associated with high grade dysplasia and cancer in colorectal adenoma. Acta Gastroenterol Latinoam 1995;25:131-5. |
|31.||Pines A, Bat L, Shemesh E. Clustering of colorectal neoplasia:characteristic of coexisting adenoma in patients with severly dysplastic polyps or invasive(malignant) polyps as compared to patients with benign adenoma or carcinomas. Postgrad Med J 1991;67:760-3. |
|32.||Disario JA, Foutch PG, Mai HD. Prevalence and malignant potential of colorectal polyps in asymptomatic, average-risk men. Am J Gastroentrol 1991;86:941-5. |
|33.||Stolfi VM., Bacaro D, Rossi P. Endoscopic polypectomy and adenoma-carcinoma sequence of the large intestine. Consideration on personal case series. G Chir 1990;11:573-8. |
|34.||Schuman BM, Simsek H, Lyons RC. The association of mutiple colonic adenoma polyps with cancer of the colon. Am J Gastroentrol 1990;85:846-9. |
|35.||Stulc JP, Petrelli NJ, Herrera L. Colorectal villous and tubulovillous adenoma equal to or greater than four centimeters. Ann Surg 1988;207:65-71. |
|36.||Haggitt RC, Glotzbach RE, Soffer EE. Prognostic factor in colorectal carcinoma arising in adenomas;implication for lesion removed by endoscopic polypectomy. Gasteroentrology 1985;89:328-36. |
[Table - 1], [Table - 2], [Table - 3]
|This article has been cited by|
||Immunohistochemical expression of ki-67 and p53 in colorectal adenomas: A clinicopathological study
| ||Nussrat, F.L. and Ali, H.H. and Hussein, H.G. and Al-Ukashi, R.J. |
| ||Oman Medical Journal. 2011; 26(4): 229-234 |
||Is cervical cancer a risk factor for colorectal neoplasia? Prevalence of colorectal adenoma in Korean patients with cervical cancer
| ||Kim, Y.J. and Kim, E.S. and Lee, J.E. and Park, W.Y. and Kwon, J.S. and Park, K.S. and Cho, K.B. and Jang, B.K. and Chung, W.J. and Hwang, J.S. and Park, J.C. |
| ||Hepato-Gastroenterology. 2011; 58(109): 1177-1181 |
|| Invasive carcinomas may arise in colorectal adenomas with high-grade dysplasia and with carcinoma in situ
| ||Rubio, C.A., Delinassios, J.G. |
| ||International Journal of Clinical and Experimental Medicine. 2010; 3(1): 41-47 |
||Clinical predictors of colorectal polyps and carcinoma in a low prevalence region: Results of a colonoscopy based study
| ||Bafandeh, Y., Khoshbaten, M., Sadat, A.T.E., Farhang, S. |
| ||World Journal of Gastroenterology. 2008; 14(10): 1534-1538 |
||Colorectal neoplasms in symptomatic patients without evidence of bleeding: A prospective study in an iranian population
| ||Bafandeh, Y. and Khoshbaten, M. and Eftekhar-Sadat, A.T. and Farhang, S. |
| ||Asian Pacific Journal of Cancer Prevention. 2007; 8(4): 485-488 |