Clinicopathological Characteristics of Serrated Polyposis Syndrome in Korea: Single Center Experience

Kim, Hyung-Keun; Seo, Kyung-Jin; Choi, Hyun Ho; Kim, Sung Soo; Chae, Hiun-Suk; Shin, Ok-Ran; Ahn, Chang Hyuck; Cho, Young-Seok

doi:https://doi.org/10.1155/2015/842876

Gastroenterology Research and Practice

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Clinical Study | Open Access

Volume 2015 | Article ID 842876 | https://doi.org/10.1155/2015/842876

Clinicopathological Characteristics of Serrated Polyposis Syndrome in Korea: Single Center Experience

Hyung-Keun Kim,¹Kyung-Jin Seo,²Hyun Ho Choi,¹Sung Soo Kim,¹Hiun-Suk Chae,¹Ok-Ran Shin,²Chang Hyuck Ahn,³and Young-Seok Cho¹

Academic Editor: Vicki Whitehall

Received31 Oct 2014

Accepted18 Mar 2015

Published12 May 2015

Abstract

Background/Aim. Serrated polyposis syndrome (SPS) is a rare condition characterized by multiple serrated polyps throughout the colon and rectum. The aim of this study was to evaluate the clinicopathological characteristics of SPS in Koreans. Methods. This retrospective analysis of prospectively collected data was performed using information from the endoscopy, clinical records, and pathology database system of Uijeongbu St. Mary’s Hospital. Consecutive patients satisfying the updated 2010 World Health Organization criteria for SPS between June 2011 and May 2014 were enrolled. Results. Of the 17,552 patients who underwent colonoscopies during the study period, 11 (0.06%) met the criteria for SPS. The mean age of these patients was 55.6 years. Ten patients (91%) were males. None had a family history of CRC or a first-degree relative with SPS. Seven patients (64%) had synchronous advanced adenoma. One patient had coexistence of SPS with CRC that was diagnosed at the initial colonoscopy. Five patients (45%) had more than 30 serrated polyps. One of the patients underwent surgery and 10 underwent endoscopic resection. Conclusion. The prevalence of SPS in this study cohort was comparable to that in Western populations. Considering the high risk of CRC, correct diagnosis and careful follow-up for SPS are necessary.

1. Introduction

Colorectal cancer (CRC) is one of the most commonly diagnosed cancers worldwide [1]. Its incidence in Asian countries is increasing rapidly, causing a major public health issue [2]. Indeed, in Korea, CRC is the second most common cancer in males and the third most common cancer in females [3]. It is known that the adenoma-carcinoma sequence is the basis for tumorigenesis and progression of CRC [4, 5]. Emerging evidence shows that one-third of CRC arises through the serrated neoplastic pathway, which is characterized by abnormal promoter CpG island hypermethylation and activation of the BRAF oncogene with or without microsatellite instability [6]. The precursor lesion in this pathway is a serrated polyp. Serrated polyps of the colorectum are characterized histologically by a serrated, saw-tooth appearance and are classified by the World Health Organization (WHO) into three general categories: hyperplastic polyp (HP), sessile serrated adenomas/polyps (SSA/Ps) with or without cytological dysplasia, and traditional serrated adenomas (TSAs) [7].

Serrated polyposis syndrome (SPS), previously called “hyperplastic polyposis syndrome,” is a rare condition, characterized by multiple serrated colorectal polyps [7]. A recent study from UK showed that SPS appeared to be relatively common (1 : 151) in patients undergoing screening colonoscopy based on fecal occult blood testing [8]. Although the exact risk of CRC in SPS is unknown, the risk of personal and familial CRC is increased in SPS. Published case series and cohort studies have reported rates of CRC from 25 to 50% at first clinical presentation in patients with SPS [9–11]. A retrospective cohort study showed that the cumulative risk of CRC under endoscopic surveillance was 7% in 5 years [9]. Thus, close endoscopic surveillance and adequate management are required to prevent malignant progression.

There are few studies regarding the prevalence or phenotypic characteristics of SPS in Asian countries. The aim of this study was to study the prevalence and clinicopathological characteristics of SPS in Korea.

2. Patients and Methods

2.1. Patients

We performed a retrospective study in 11 patients with SPS identified at Uijeongbu St. Mary’s Hospital between June 2011 and May 2014. The following WHO criteria were used to identify SPS: (1) at least five serrated polyps proximal to the sigmoid colon with two or more of them being >10 mm, (2) any number of serrated polyps proximal to the sigmoid colon in an individual who has a first-degree relative with serrated polyposis, or (3) >20 serrated polyps of any size, but distributed throughout the colon [7]. We excluded cases with a family history of familial adenomatous polyposis (FAP), hereditary nonpolyposis colorectal cancer (HNPCC), or familial colorectal cancer, surgical resection of the colon or rectum, inflammatory bowel disease, and incomplete examination of the entire colon due to poor bowel preparation or technical difficulties. The study protocol was approved by the Institutional Research Ethics Board of Uijeongbu St. Mary’s Hospital (IRB number UC14SISI0105). The study was conducted in accordance with the Helsinki Declaration.

2.2. Data Collection and Analysis

This retrospective analysis of prospectively collected data was performed using information from the endoscopy, clinical records, and pathology database system of Uijeongbu St. Mary’s Hospital. Demographic data of patients included age, gender, smoking habits, comorbidities, personal and family history of CRC or other neoplasia, body mass index (BMI), and surgical history. Colonoscopy reports regarding characteristic of polyps (number and size of serrated polyps, polyp distribution, resection for polyps, and synchronous lesions) and diagnostic criteria met were collected.

Based on the WHO classification, serrated colorectal polyps were classified histologically as HPs, SSA/Ps with or without cytological dysplasia, or TSAs [7]. SSA/Ps are characterized by the presence of distorted and dilated crypts, especially at the base, along with excess serration near the base. The crypt often appears with a “boot” or “L” shape. TSAs are characterized by a protuberant or pedunculated growth pattern with distorted villiform configurations. They have columnar cells with abundant eosinophilic cytoplasm and centrally located elongated nuclei with an even chromatin pattern. The colon was divided into the distal (rectum, sigmoid colon, and descending colon) and proximal colon (splenic flexure, transverse colon, hepatic flexure, ascending colon, and cecum). Because information regarding family history is often subjective and not always reliable, none of the patients with SPS was diagnosed on the basis of the second WHO criterion (any number of serrated polyps proximal to the sigmoid colon in an individual who has a first-degree relative with serrated polyposis).

3. Results

In total, 17,552 subjects underwent colonoscopies at Uijeongbu St. Mary’s Hospital during the study period. Among them, 11 (0.06%) patients met the criteria for SPS (Table 1, Figure 1). Ten were males and one was female; their mean age at the time of diagnosis was (range 35–72) years. Demographic data are shown in Table 1. Of these 11 patients, 5 met WHO criterion 1, and 6 met criterion 3. Five patients (45%) had more than 30 serrated polyps, and the average size of the largest polyp was 22 mm. In total, 125 polyps were removed with conventional polypectomy or endoscopic mucosal resection in the 11 SPS patients. HPs comprised 36 (28.8%), SSA/Ps 49 (39.2%), TSAs 3 (2.4%), and tubular adenomas 37 (29.6%) of the 125 polyps. A pancolonic distribution of polyps was shown in nine (82%) patients, and proximal colon distribution was observed in the remaining two (18%) patients. Seven patients (64%) had synchronous advanced adenomas. There was no difference in the pathological characteristics of polyps of patients meeting criterion 1 versus those meeting criterion 3. One patient had coexisting SPS with CRC that was diagnosed at the initial colonoscopy. This CRC was serrated adenocarcinoma histopathologically (Figure 2). One underwent surgery and 10 underwent endoscopic resections.

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In total, seven (64%) patients were current or former smokers. None had a family history of CRC or a first-degree relative with SPS. All of the patients underwent esophagogastroduodenoscopy (EGD). No patients had duodenal polyps or gastric adenomas on examination. Three patients (27%) had other extracolonic cancers or hematologic malignancies: one with hepatocellular carcinoma (HCC) associated with chronic hepatitis B, one with lung cancer, and one with myelodysplastic syndrome (MDS).

4. Discussion

SPS is a disease entity that is not well recognized, especially in Asian countries. Its genetic background and natural course have not been well characterized. In our study, we evaluated the clinicopathological characteristics of patients meeting the updated WHO criteria for the diagnosis of SPS. The prevalence of SPS in our study cohort was 0.06% (1 : 1,596). Previous reports from Western countries have shown variable results for the prevalence of SPS. Lockett and Atkin reported that the prevalence of SPS was relatively low (1 : 3,000; 0.033%) in the general UK population [12]. However, this result may have been underestimated because colonoscopy was performed only in patients with more than 20 polyps on flexible sigmoidoscopy. Orlowska et al. reported the frequency of SPS to be 0.056% (28/50,148) in asymptomatic patients who participated in colonoscopy-based CRC screening [13]. This result was similar to that of our study. However, recent studies reported that the prevalence of SPS was estimated between 1 : 151 and 1 : 294 in patients who underwent index screening colonoscopies based on fecal occult blood testing [8, 14]. These differences may be due to the differences in study design, patient populations, and other confounding factors. There have been few studies on the prevalence of SPS in Asia. Miwata et al. first reported the prevalence of SPS in Asia [15]. Of 73,608 Japanese patients who underwent colonoscopies in 14 hospitals, 10 (0.014%) met the WHO criteria for the diagnosis of SPS. However, the frequency of SPS in patients who underwent endoscopic resections was not so rare (0.38%) in this study. Vemulapalli and Rex reported that SPS was common in patients referred for resection of large sessile colorectal polyps, and it was frequently unrecognized [16]. Of the 529 patients, 20 were diagnosed as having SPS according to the WHO criteria, but only one patient was suspected by a referring physician. In our 11 patients with SPS, 5 were referred from local physicians for the resection of large colorectal polyps. All referred patients were undiagnosed at their first colonoscopy. A recent study demonstrated that patients with SPS underwent a median of four colonoscopies before satisfying the WHO criteria, and at least two pathologically confirmed serrated lesions are required to identify patients satisfying the WHO criteria for SPS [17]. Because SPS may be underdiagnosed due to lack of awareness, further studies are necessary to confirm its prevalence in Asians.

Previous studies showed that SPS has a near-equal gender distribution [9, 15, 18]. However, this study showed a strong male predominance in patients with SPS. The reason for this gender difference remains unclear. Recent studies from Western countries showed that most patients met WHO criterion 3 rather than criterion 1 [18, 19]. However, such a finding was not observed in our study or Japanese study, and this may be due to ethnic and/or racial differences [15]. Additionally, a recent study showed that there was no significant demographic, pathological, or molecular difference between patients meeting criterion 1 and patients meeting criterion 3, with the only exception of a greater likelihood of a family history of CRC and colonic polyps in patients meeting criterion 3 [19]. Further studies to compare clinical criteria with genotype are necessary.

The risk of personal and familial CRC is known to be increased in SPS. Previous studies showed that about 25–70% of SPS patients had CRC at the initial presentation or during follow-up [15]. A retrospective multicenter study showed that CRC was detected during surveillance in 5 of 77 SPS patients after a median follow-up of 1.3 years, and the cumulative risk of CRC under surveillance was 7% at 5 years [9]. In our study, only one patient (9%) had CRC at the initial presentation. This finding may be attributed to the short interval in colonoscopies performed and racial differences. The molecular basis of CRC development in patients with SPS remains unclear, but the importance of the serrated neoplastic pathway of carcinogenesis in SPS has been suggested [19, 20]. A recent prospective cohort study demonstrated that CRC was not detected in SPS patients during annual surveillance after endoscopic clearance of all polyps ≥ 3 mm, and the cumulative risks of detecting of CRC, advanced adenoma, or large serrated polyps (≥10 mm) were 0%, 9%, and 34%, respectively [21]. This result suggests that CRC development in SPS patients may be decreased by close endoscopic surveillance with removal of polyps ≥ 3 mm. However, further studies are needed to identify the most appropriate time interval for endoscopic surveillance and high risk patients requiring prophylactic surgery.

Additionally, emerging evidence shows that first-degree relatives of patients with SPS have an increased risk of developing CRC. Retrospective cohort studies reported an approximately fivefold increased incidence of CRC in first-degree relatives of patients with SPS compared with the general population [22–24]. Moreover, a recent study demonstrated that single screening colonoscopy in first-degree relatives of patients with SPS detected one or more significant polyps (43%), multiple polyps (9%), and SPS (14%) [25]. This suggests that a colonoscopy screening program for these individuals is necessary. None of the first-degree relatives of patients with SPS were diagnosed as having SPS in our study or a Japanese study [15]. However, the reason may be that colonoscopy was not performed in all first-degree relatives.

In the present study, 64% of patients with SPS were current or former smokers, which was higher than the prevalence of 46.2% of ever-smokers based on the data of the Korean National Health and Nutrition Examination Surveys [26]. A recent study showed that smoking at least 20 pack-years was strongly associated with SSAs of any and large sizes [27]. SPS patients also were significantly more likely to be current smokers than were either colonoscopy controls or population controls in another study [28]. Further studies should examine the effects of smoking in SPS patients in more detail.

Hereditary CRC syndromes (FAP and HNPCC) and hamartomatous polyposis syndromes (Peutz-Jeghers syndrome, juvenile polyposis syndrome, and Cowden syndrome) carry significant risks for extracolonic malignancies [29]. Although gastric neoplasia is a common disease in Korea, none of our patients had duodenal polyps or gastric adenomas on EGD. This result is similar to those from previous Western studies, suggesting that SPS patients may not be at increased risk of gastroduodenal polyps [30, 31]. Additionally, the present study showed that 27% had a history of extracolonic cancers or hematologic malignancies. Although HCC and lung cancer are common in the general population, SPS in MDS patients has not been reported. Further research is needed because studies regarding extracolonic tumors reported in SPS patients have shown inconsistent results [11, 31].

In conclusion, the prevalence of SPS in our cohort was comparable to that in Western populations. However, clinicopathological characteristics of patients with SPS showed some differences, including a strong male predominance and the WHO diagnostic criterion met. Additionally, SPS was almost unrecognized by referring physicians. Further large-scale multicenter studies are needed to confirm the prevalence of SPS in Asia. Considering the high risk of CRC, correct diagnosis and careful follow-up for SPS and colonoscopy screening for first-degree relatives of patients with SPS are necessary.

Disclosure

The study sponsor has no contribution in the study design, analysis, interpretation of data, and publication.

Conflict of Interests

All authors have no conflict of interests to declare.

Authors’ Contribution

Hyung-Keun Kim and Kyung-Jin Seo contributed equally to this work.

Acknowledgment

This research was in part supported by a grant from Hanmi Pharmaceuticals, Republic of Korea.

References

J. Ferlay, H.-R. Shin, F. Bray, D. Forman, C. Mathers, and D. M. Parkin, “Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008,” International Journal of Cancer, vol. 127, no. 12, pp. 2893–2917, 2010.
View at: Publisher Site | Google Scholar
I. Hyodo, H. Suzuki, K. Takahashi et al., “Present status and perspectives of colorectal cancer in Asia: colorectal cancer working group report in 30th Asia-Pacific cancer conference,” Japanese Journal of Clinical Oncology, vol. 40, supplement 1, pp. i38–i43, 2010.
View at: Publisher Site | Google Scholar
K. W. Jung, S. Park, H. J. Kong et al., “Cancer statistics in Korea: incidence, mortality, survival, and prevalence in 2009,” Cancer Research and Treatment, vol. 44, no. 1, pp. 11–24, 2012.
View at: Publisher Site | Google Scholar
E. R. Fearon and B. Vogelstein, “A genetic model for colorectal tumorigenesis,” Cell, vol. 61, no. 5, pp. 759–767, 1990.
View at: Publisher Site | Google Scholar
S. D. Markowitz and M. M. Bertagnolli, “Molecular origins of cancer: molecular basis of colorectal cancer,” The New England Journal of Medicine, vol. 361, no. 25, pp. 2449–2460, 2009.
View at: Publisher Site | Google Scholar
D. K. Rex, D. J. Ahnen, J. A. Baron et al., “Serrated lesions of the colorectum: review and recommendations from an expert panel,” The American Journal of Gastroenterology, vol. 107, no. 9, pp. 1314–1330, 2012.
View at: Publisher Site | Google Scholar
D. C. Snover, D. Ahnen, R. W. Burt, and R. D. Odze, “Serrated polyps of the colon and rectum and serrated (‘hyperplastic’) polyposis,” in WHO Classification of Tumours. Pathology and Genetics. Tumours of the Digestive System, F. T. Bosman, F. Carneiro, R. H. Hruban, and N. Theise, Eds., Springer, Berlin, Germany, 2010.
View at: Google Scholar
S. Biswas, A. J. Ellis, R. Guy, H. Savage, K. Madronal, and J. E. East, “High prevalence of hyperplastic polyposis syndrome (serrated polyposis) in the NHS bowel cancer screening programme,” Gut, vol. 62, no. 3, p. 475, 2013.
View at: Publisher Site | Google Scholar
K. S. Boparai, E. M. H. Mathus-Vliegen, J. J. Koornstra et al., “Increased colorectal cancer risk during follow-up in patients with hyperplastic polyposis syndrome: a multicentre cohort study,” Gut, vol. 59, no. 8, pp. 1094–1100, 2010.
View at: Publisher Site | Google Scholar
L. G. Carvajal-Carmona, K. M. Howarth, M. Lockett et al., “Molecular classification and genetic pathways in hyperplastic polyposis syndrome,” Journal of Pathology, vol. 212, no. 4, pp. 378–385, 2007.
View at: Publisher Site | Google Scholar
M. F. Kalady, A. Jarrar, B. Leach et al., “Defining phenotypes and cancer risk in hyperplastic polyposis syndrome,” Diseases of the Colon and Rectum, vol. 54, no. 2, pp. 164–170, 2011.
View at: Publisher Site | Google Scholar
M. Lockett and W. S. Atkin, “Hyperplastic polyposis: prevalence and cancer risk,” Gut, vol. 49, supplement 1, p. A4, 2001.
View at: Google Scholar
J. Orlowska, M. Kiedrowski, F. M. Kaminski, J. Regula, and E. Butruk, “Hyperplastic polyposis syndrome in asymptomatic patients: the results from the colorectal-cancer screening program,” Virchows Archiv, vol. 455, supplement 1, p. S47, 2009.
View at: Google Scholar
L. Moreira, M. Pellisé, S. Carballal et al., “High prevalence of serrated polyposis syndrome in FIT-based colorectal cancer screening programmes,” Gut, vol. 62, no. 3, pp. 476–477, 2013.
View at: Publisher Site | Google Scholar
T. Miwata, T. Hiyama, S. Oka et al., “Clinicopathologic features of hyperplastic/serrated polyposis syndrome in Japan,” Journal of Gastroenterology and Hepatology, vol. 28, no. 11, pp. 1693–1698, 2013.
View at: Publisher Site | Google Scholar
K. C. Vemulapalli and D. K. Rex, “Failure to recognize serrated polyposis syndrome in a cohort with large sessile colorectal polyps,” Gastrointestinal Endoscopy, vol. 75, no. 6, pp. 1206–1210, 2012.
View at: Publisher Site | Google Scholar
V. W. Hui, E. Steinhagen, R. A. Levy et al., “Utilization of colonoscopy and pathology reports for identifying patients meeting the world health organization criteria for serrated polyposis syndrome,” Diseases of the Colon & Rectum, vol. 57, no. 7, pp. 846–850, 2014.
View at: Publisher Site | Google Scholar
C. Rosty, D. D. Buchanan, M. D. Walsh et al., “Phenotype and polyp landscape in serrated polyposis syndrome: a series of 100 patients from genetics clinics,” The American Journal of Surgical Pathology, vol. 36, no. 6, pp. 876–882, 2012.
View at: Publisher Site | Google Scholar
C. Guarinos, C. Sánchez-Fortún, M. Rodríguez-Soler et al., “Clinical subtypes and molecular characteristics of serrated polyposis syndrome,” Clinical Gastroenterology and Hepatology, vol. 11, no. 6, pp. 705–711, 2013.
View at: Publisher Site | Google Scholar
K. S. Boparai, E. Dekker, M. M. Polak, A. R. Musler, S. van Eeden, and C. J. M. van Noesel, “A serrated colorectal cancer pathway predominates over the classic WNT pathway in patients with hyperplastic polyposis syndrome,” The American Journal of Pathology, vol. 178, no. 6, pp. 2700–2707, 2011.
View at: Publisher Site | Google Scholar
Y. Hazewinkel, K. M. A. J. Tytgat, S. van Eeden et al., “Incidence of colonic neoplasia in patients with serrated polyposis syndrome who undergo annual endoscopic surveillance,” Gastroenterology, vol. 147, no. 1, pp. 88–95, 2014.
View at: Publisher Site | Google Scholar
P. Lage, M. Cravo, R. Sousa et al., “Management of Portuguese patients with hyperplastic polyposis and screening of at-risk first-degree relatives: a contribution for future guidelines based on a clinical study,” The American Journal of Gastroenterology, vol. 99, no. 9, pp. 1779–1784, 2004.
View at: Publisher Site | Google Scholar
K. S. Boparai, J. B. Reitsma, V. Lemmens et al., “Increased colorectal cancer risk in first-degree relatives of patients with hyperplastic polyposis syndrome,” Gut, vol. 59, no. 9, pp. 1222–1225, 2010.
View at: Publisher Site | Google Scholar
A. K. Win, R. J. Walters, D. D. Buchanan et al., “Cancer risks for relatives of patients with serrated polyposis,” The American Journal of Gastroenterology, vol. 107, no. 5, pp. 770–778, 2012.
View at: Publisher Site | Google Scholar
Y. Hazewinkel, J.-J. Koornstra, K. S. Boparai et al., “Yield of screening colonoscopy in first-degree relatives of patients with serrated polyposis syndrome,” Journal of Clinical Gastroenterology, 2014.
View at: Publisher Site | Google Scholar
W. J. Kim, J. S. Song, D. W. Park et al., “The effects of secondhand smoke on chronic obstructive pulmonary disease in nonsmoking Korean adults,” The Korean Journal of Internal Medicine, vol. 29, no. 5, pp. 613–619, 2014.
View at: Publisher Site | Google Scholar
J. C. Anderson, P. Rangasamy, T. Rustagi et al., “Risk factors for sessile serrated adenomas,” Journal of Clinical Gastroenterology, vol. 45, no. 8, pp. 694–699, 2011.
View at: Publisher Site | Google Scholar
K. Wallace, M. V. Grau, D. Ahnen et al., “The association of lifestyle and dietary factors with the risk for serrated polyps of the colorectum,” Cancer Epidemiology Biomarkers and Prevention, vol. 18, no. 8, pp. 2310–2317, 2009.
View at: Publisher Site | Google Scholar
K. Sweet, J. Willis, X.-P. Zhou et al., “Molecular classification of patients with unexplained hamartomatous and hyperplastic polyposis,” Journal of the American Medical Association, vol. 294, no. 19, pp. 2465–2473, 2005.
View at: Publisher Site | Google Scholar
D. L. Edelstein, J. E. Axilbund, L. M. Hylind et al., “Serrated polyposis: rapid and relentless development of colorectal neoplasia,” Gut, vol. 62, no. 3, pp. 404–418, 2013.
View at: Publisher Site | Google Scholar
K. W. Jasperson, P. Kanth, A. C. Kirchhoff et al., “Serrated polyposis: colonic phenotype, extracolonic features, and familial risk in a large cohort,” Diseases of the Colon and Rectum, vol. 56, no. 11, pp. 1211–1216, 2013.
View at: Publisher Site | Google Scholar

Copyright

Copyright © 2015 Hyung-Keun Kim et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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