Journal of Peking University (Health Sciences) ›› 2021, Vol. 53 ›› Issue (6): 1122-1127. doi: 10.19723/j.issn.1671-167X.2021.06.019

Previous Articles     Next Articles

Analysis of endoscopic and pathological features of gastric adenomatous polyps and risk factors for canceration

NIU Zhan-yue,XUE Yan,ZHANG Jing,ZHANG He-jun,DING Shi-gang()   

  1. Department of Gastroenterology, Peking University Third Hospital, Beijing 100191, China
  • Received:2020-03-31 Online:2021-12-18 Published:2021-12-13
  • Contact: Shi-gang DING E-mail:dingshigang222@163.com

RICH HTML

  

Abstract:

Objective: To investigate the endoscopic and pathological characteristics of gastric adenomatous polyps and to assess the potential risk factors for canceration of gastric adenomatous polyps. Methods: The endoscopic and pathological characteristics of the patients with gastric adenomatous polyps from January 1, 2005 to December 31, 2019 were summarized retrospectively, and the risk factors of canceration were analyzed. Results: A total of 125 patients with gastric adenomatous polyps were included, 51.20% of whom were females. The average age was (66.7±12.3) years. 64.80% of patients with gastric adenomatous polyps equal or more than 65 years old, and only 5.60% of the patients less than 45 years old. Adenomatous polyps were mostly distributed in the corpus and antrum with 40.80% and 32.80%, respectively. The majority of them were single (90.40%) and sessile (76.81%). 65.4% of adenomatous polyps were no more than 1.0 cm in diameter, and 23.20% of patients with adenomatous polyps were combined with hyperplastic polyps and/or fundus glandular polyps, and 1.60% had both pathological types of polyps. 58.62% (17/29) patients with hyperplastic polyps and/or fundus glandular polyps had multiple polyps. 1.60% (2/125) of the patients had gastric neuroendocrine tumor of G1 stage. Synchronous gastric cancer was detected in 13.60% (17/125) of the patients with adenomatous polyps, and the proportion of low-grade intraepithelial neoplasia was 18.40% (23/125). The main types of synchronous gastric cancer were progressive (70.59%) and undifferentiated (66.67%). Chronic atrophic gastritis with intestinal metaplasia was found in 52.80% of the patients, and autoimmune gastritis accounted for 11.20%. The positive rate of Helicobacter pylori was 21.60%. The canceration rate of gastric adenomatous polyps was 20.80%. The cancer was mainly differentiated, but there was sigmoid ring cell carcinoma as well. Diameter of >1.0 cm (OR=5.092, 95%CI: 1.447-17.923, P=0.011), uneven surface morphology and erosion (OR=13.749, 95%CI: 1.072-176.339, P=0.044) were independent risk factors of adenomatous polyps. Conclusion: The synchronous gastric cancer is common and the canceration of gastric adenomatous polyps is high with diameter and surface morphology as independent risk factors. We should pay attention to the identification of the pathological types of polyps and the evaluation of the whole gastric mucosa during the endoscopic examination.

Key words: Adenomatous polyps, Neoplasms, multiple primary, Endoscopy, gastrointestinal, Risk factors

CLC Number: 

  • R735.2

Table 1

Basic data of gastroscopy and gastric adenomatous polyp"

Year Gastroscopy, n Gastric adenomatous polyp, n (%)
2005 4 389 3 (0.07)
2006 7 185 8 (0.11)
2007 8 511 10 (0.12)
2008 9 192 7 (0.08)
2009 11 116 6 (0.05)
2010 11 348 4 (0.04)
2011 12 179 7 (0.06)
2012 13 772 13 (0.09)
2013 14 890 9 (0.06)
2014 16 404 8 (0.05)
2015 16 007 4 (0.02)
2016 17 592 13 (0.07)
2017 17 641 6 (0.03)
2018 19 422 17 (0.09)
2019 19 153 10 (0.05)
Total 198 801 125 (0.06)

Table 2

Gastroscopic features of adenomatous polyp"

Gastroscopic features n (%)
Location
Cardia 10 (8.00)
Fundus 10 (8.00)
Body 51 (40.80)
Incisura angularis 5 (4.00)
Antral 41 (32.80)
Multiple 8 (6.40)
Number
Single 113 (90.40)
Multiple (n≥2) 12 (9.60)
Diameter/cm
≤0.5 32 (23.19)
>0.5-1.0 59 (42.75)
>1.0-1.5 15 (10.87)
>1.5-2.0 15 (10.87)
>2.0-2.5 5 (3.62)
>2.5-3.0 3 (2.17)
>3.0 9 (6.52)
Yamada type
73 (52.90)
33 (23.91)
20 (14.49)
12 (8.70)

Figure 1

Endoscopic and pathological manifestations of adenomatous polyps and canceration A, adenomatous polyp of antrum, smooth surface, same color as the surrounding mucosa; B, pathological manifestations of adenomatous polyp (HE ×10); C, canceration of cardiac adenomatous polyp with rough and reddish surface; D, the pathology of cancerous adenomatous polyp (HE ×20)."

Table 3

Comorbid gastric disease with adenomatous polyp"

Disease n (%)
Other types of polyp
Fundic gland polyp
Single 0 (0)
Multiple 3 (2.40)
Hyperplastic polyp
Single 12 (9.60)
Multiple 12 (9.60)
Both 2 (1.60)
Neuroendocrine tumor
G1 2 (1.60)
G2 0 (0)
G3 0 (0)
Low grade intraepithelial neoplasia 23 (18.40)
High grade intraepithelial neoplasia 3 (2.40)
Early cancer 2 (1.60)
Advanced gastric cancer
Differentiated 4 (3.20)
Undifferentiated 8 (6.40)

Table 4

The pathological features of adenomatous polyp"

Pathological features n (%)
Polyp
High grade intraepithelial neoplasia 10 (8.00)
Canceration 16 (12.80)
Background
Chronic superficial gastritis 24 (19.20)
Autoimmune gastritis 14 (11.20)
Chronic atrophic gastritis 21 (16.80)
Chronic atrophic gastritis with intestinal metaplasia 66 (52.80)
Helicobacter pylori 27 (21.60)

Table 5

Risk factors for canceration of adenomatous polyp"

Risk factors Canceration, n Non-canceration, n χ2 P value
Gender
Male 9 52 2.644 0.104
Female 17 47
Age
<45 0 7 6.353 0.174
45-54 2 13
55-64 3 19
65-74 14 30
≥75 7 30
Location
Cardia 3 7 8.789 0.118
Fundus 4 6
Body 7 44
Incisura angularis 1 4
Antral 7 34
Multiple 4 4
Number
Single 21 92 3.509 0.061
Multiple (n≥2) 5 7
Diameter/cm
≤1.0 7 74 28.868 <0.001
1.1-2.0 7 20
2.1-3.0 5 3
>3.0 7 2
Type
Pedicless 16 80 4.291 0.038
Pedicled 10 19
Color
Normal 11 57 2.138 0.343
Red 11 33
White 4 9
Surface
Smooth 7 65 20.538 0.001
Rough 8 18
Lobulated 5 8
Erosion 1 6
Rough and erosion 3 1
Lobulated and erosion 2 1
Background
Chronic superficial gastritis 2 22 4.303 0.231
Autoimmune gastritis 4 10
Chronic atrophic gastritis 3 18
Chronic atrophic gastritis with intestinal metaplasia 17 49
Helicobacter pylori
Positive 5 22 0.125 0.724
Negative 21 76

Table 6

Multivariate Logistic regression analysis of risk factors for canceration"

Risk factors OR (95%CI) P value
Diameter/cm
≤1.0 1
>1.0 5.092 (1.447-17.923) 0.011
Type
Pedicled 1
Pedicless 1.120 (0.343-3.654) 0.852
Surface
Normal 1
Rough 1.850 (0.496-6.895) 0.360
Lobulated 2.339 (0.489-11.183) 0.287
Erosion 1.641 (0.154-17.519) 0.682
Rough and erosion 13.749 (1.072-176.339) 0.044
Lobulated and erosion 5.617 (0.389-81.126) 0.205
[1] Carmack SW, Genta RM, Schuler CM, et al. The current spectrum of gastric polyps: A 1-year national study of over 120,000 patients[J]. Am J Gastroenterol, 2009, 104(6):1524-1532.
doi: 10.1038/ajg.2009.139
[2] Corral JE, Keihanian T, Diaz LI, et al. Management patterns of gastric polyps in the United States[J]. Frontline Gastroenterol, 2019, 10(1):16-23.
doi: 10.1136/flgastro-2017-100941
[3] Enestvedt BK, Chandrasekhara V, Ginsberg GG. Endoscopic ultrasonographic assessment of gastric polyps and endoscopic mucosal resection[J]. Curr Gastroenterol Rep, 2012, 14(6):497-503.
doi: 10.1007/s11894-012-0292-2 pmid: 23001857
[4] Velázquez-Dohorn ME, López-Durand CF, Gamboa-Domínguez A. Changing trends in gastric polyps[J]. Rev Invest Clin, 2018, 70(1):40-45.
doi: 10.24875/RIC.17002430 pmid: 29513301
[5] Castro R, Pimentel-Nunes P, Dinis-Ribeiro M. Evaluation and management of gastric epithelial polyps[J]. Best Pract Res Clin Gastroenterol, 2017, 31(4):381-387.
doi: S1521-6918(17)30060-4 pmid: 28842047
[6] Chen WC, Wallace MB. Endoscopic management of mucosal lesions in the gastrointestinal tract[J]. Expert Rev Gastroenterol Hepatol, 2016, 10(4):481-495.
doi: 10.1586/17474124.2016.1122520
[7] Banks M, Graham D, Jansen M, et al. British Society of Gastroenterology guidelines on the diagnosis and management of patients at risk of gastric adenocarcinoma[J]. Gut, 2019, 68(9):1545-1575.
[8] Laxén F, Sipponen P, Iham?ki T. Gastric polyps: their morphological and endoscopical characteristics and relation to gastric carcinoma[J]. Acta Pathol Microbiol Immunol Scand A, 1982, 90(3):221-228.
pmid: 7102316
[9] Borch K, Skarsgard J, Franzen L, et al. Benign gastric polyps: Morphological and functional origin[J]. Dig Dis Sci, 2003, 48(7):1292-1297.
doi: 10.1023/A:1024150924457
[10] Zhao G, Xue M, Hu Y, et al. How commonly is the diagnosis of gastric low grade dysplasia upgraded following endoscopic resection? A meta-analysis[J]. PLoS One, 2015, 10(7):e0132699.
doi: 10.1371/journal.pone.0132699
[11] de Vries AC, van Grieken NC, Looman CW, et al. Gastric cancer risk in patients with premalignant gastric lesions: A nationwide cohort study in the Netherlands[J]. Gastroenterology, 2008, 134(4):945-952.
doi: 10.1053/j.gastro.2008.01.071
[12] Meining A, Riedl B, Stolte M. Features of gastritis predisposing to gastric adenoma and early gastric cancer[J]. J Clin Pathol, 2002, 55(10):770-773.
pmid: 12354805
[13] Zhang H, Jin Z, Cui R, et al. Autoimmune metaplastic atrophic gastritis in chinese: A study of 320 patients at a large tertiary medical center[J]. Scand J Gastroenterol, 2017, 52(2):150-156.
doi: 10.1080/00365521.2016.1236397
[14] Zhang H, Nie X, Song Z, et al. Hyperplastic polyps arising in autoimmune metaplastic atrophic gastritis patients: Is this a distinct clinicopathological entity[J]. Scand J Gastroenterol, 2018, 53(10/11):1186-1193.
doi: 10.1080/00365521.2018.1514420
[15] Suzuki S, Gotoda T, Suzuki H, et al. Morphologic and histologic changes in gastric adenomas after Helicobacter pylori eradication: A long-term prospective analysis[J]. Helicobacter, 2015, 20(6):431-437.
doi: 10.1111/hel.12218 pmid: 25704290
[16] Malfertheiner P, Megraud F, O’Morain CA, et al. Management of Helicobacter pylori infection: the Maastricht V/Florence Consensus Report[J]. Gut, 2017, 66(1):6-30.
doi: 10.1136/gutjnl-2016-312288 pmid: 27707777
[17] Pimentel-Nunes P, Dinis-Ribeiro M, Ponchon T, et al. Endosco-pic submucosal dissection: European Society of Gastrointestinal Endoscopy (ESGE) Guideline[J]. Endoscopy, 2015, 47(9):829-854.
doi: 10.1055/s-0034-1392882 pmid: 26317585
[1] Jiafu JI, Jingtao WEI, Ke JI, Zhaode BU. Bottlenecks and breakthroughs in gastric cancer diagnosis and treatment: Towards a new era of precision and intelligent integration [J]. Journal of Peking University (Health Sciences), 2026, 58(2): 231-238.
[2] Jiale GAO, Zhongtao ZHANG. Current status and future perspectives of precision treatment for locally advanced rectal cancer [J]. Journal of Peking University (Health Sciences), 2026, 58(2): 247-250.
[3] Youdong LIU, Yajun LYU, Jie CHEN, Mingde ZANG, Hongda PAN, Xiaowen LIU, Jun LU, Fenglin LIU. Clinical efficacy and safety of totally laparoscopic subtotal gastrectomy with cardia-gastric fundus preservation in middle-upper gastric cancer [J]. Journal of Peking University (Health Sciences), 2026, 58(2): 301-306.
[4] Hui WEI, Jingfeng ZHANG, Zhongqiang YAO, Jinxia ZHAO. Clinical characteristics and relevant factors of rheumatoid arthritis patients with anemia of chronic disease [J]. Journal of Peking University (Health Sciences), 2026, 58(2): 307-312.
[5] Qianying WEN, Liqing ZHANG, Anlin QIN, Xiaofeng LI. Small intestinal bacterial overgrowth and inflammatory factor expression levels in patients with asymptomatic hyperuricemia [J]. Journal of Peking University (Health Sciences), 2026, 58(2): 313-318.
[6] Jie ZHAO, Chun FU, Xiujuan ZHAO, Haiyan XUE, Shu LI, Zhenzhou WANG, Fengxue ZHU. Risk factors for ventilator-associated pneumonia in patients with chest trauma in intensive care unit [J]. Journal of Peking University (Health Sciences), 2026, 58(2): 351-358.
[7] Jialin LI, Liqiao CHEN, Jiatian TANG, Yan WU, Anqiang WANG. Conversion therapy for hepatoid adenocarcinoma of the stomach: A case report [J]. Journal of Peking University (Health Sciences), 2026, 58(2): 399-404.
[8] Bin LI, Han LIANG. Robotic gastrectomy: Research progress and practical challenges [J]. Journal of Peking University (Health Sciences), 2026, 58(2): 416-422.
[9] Yanhua LIU, Min LU, Xuyang ZHAO, Kuan'gen ZHANG, Rui WU, Fang MEI, Zhihao DAI, Jiangfeng YOU, Fei PEI. Effect of dephosphorylation of tumor metastasis suppressor gene LASS2 on vacuolar ATPase activity and invasiveness of prostate cancer [J]. Journal of Peking University (Health Sciences), 2025, 57(6): 1113-1123.
[10] Bowen LI, Qiang ZHANG, Yixin SUN. Establishment and validation of a risk prediction model for scoliosis after Nuss procedure in children and young adults with pectus excavatum [J]. Journal of Peking University (Health Sciences), 2025, 57(5): 941-946.
[11] Xiaoyong YANG, Fan ZHANG, Lulin MA, Cheng LIU. Clinical characteristics and influencing factors of extraglandular invasion of prostatic ductal adenocarcinoma [J]. Journal of Peking University (Health Sciences), 2025, 57(5): 956-960.
[12] Jiaxin NING, Haoran WANG, Shuhang LUO, Jibo JING, Jianye WANG, Huimin HOU, Ming LIU. Multi-omics analysis of the relationship between oxidative stress-related gene and prostate cancer [J]. Journal of Peking University (Health Sciences), 2025, 57(4): 633-643.
[13] Zeyuan WANG, Shuanbao YU, Haoke ZHENG, Jin TAO, Yafeng FAN, Xuepei ZHANG. A preoperative prediction model for pelvic lymph node metastasis in prostate cancer: Integrating clinical characteristics and multiparametric MRI [J]. Journal of Peking University (Health Sciences), 2025, 57(4): 684-691.
[14] Wei LIU, Wen GUO, Zhe GUO, Chunyan LI, Yunlong LI, Siqi LIU, Liang ZHANG, Hui SONG. Risk factors associated with non-radiographic bone erosion in patients with gout [J]. Journal of Peking University (Health Sciences), 2025, 57(4): 735-739.
[15] Shuai LIU, Zhuo LIU, Yunhe GUAN, Guoliang WANG, Xiaojun TIAN, Hongxian ZHANG, Lei LIU, Lulin MA, Shudong ZHANG. Robot-assisted laparoscopic inferior vena cava segmental resection for renal tumor with tumor thrombus invading the vascular wall [J]. Journal of Peking University (Health Sciences), 2025, 57(4): 796-802.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!